|Dividing the spoils of growth and the cell cycle: The fission yeast as a model for the study of cytokinesis.|
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|PMID: 21246752 Owner: NLM Status: MEDLINE|
|Cytokinesis is the final stage of the cell cycle, and ensures completion of both genome segregation and organelle distribution to the daughter cells. Cytokinesis requires the cell to solve a spatial problem (to divide in the correct place, orthogonally to the plane of chromosome segregation) and a temporal problem (to coordinate cytokinesis with mitosis). Defects in the spatiotemporal control of cytokinesis may cause cell death, or increase the risk of tumor formation [Fujiwara et al., 2005 (Fujiwara T, Bandi M, Nitta M, Ivanova EV, Bronson RT, Pellman D. 2005. Cytokinesis failure generating tetraploids promotes tumorigenesis in p53-null cells. Nature 437:1043–1047); reviewed by Ganem et al., 2007 (Ganem NJ, Storchova Z, Pellman D. 2007. Tetraploidy, aneuploidy and cancer. Curr Opin Genet Dev 17:157–162.)]. Asymmetric cytokinesis, which permits the generation of two daughter cells that differ in their shape, size and properties, is important both during development, and for cellular homeostasis in multicellular organisms [reviewed by Li, 2007 (Li R. 2007. Cytokinesis in development and disease: variations on a common theme. Cell Mol Life Sci 64:3044–3058)]. The principal focus of this review will be the mechanisms of cytokinesis in the mitotic cycle of the yeast Schizosaccharomyces pombe. This simple model has contributed significantly to our understanding of how the cell cycle is regulated, and serves as an excellent model for studying aspects of cytokinesis. Here we will discuss the state of our knowledge of how the contractile ring is assembled and disassembled, how it contracts, and what we know of the regulatory mechanisms that control these events and assure their coordination with chromosome segregation.|
|Anupama Goyal; Masak Takaine; Viesturs Simanis; Kentaro Nakano|
|Type: Journal Article; Research Support, Non-U.S. Gov't; Review|
|Title: Cytoskeleton (Hoboken, N.J.) Volume: 68 ISSN: 1949-3592 ISO Abbreviation: Cytoskeleton (Hoboken) Publication Date: 2011 Feb|
|Created Date: 2011-01-19 Completed Date: 2011-04-25 Revised Date: 2013-06-30|
Medline Journal Info:
|Nlm Unique ID: 101523844 Medline TA: Cytoskeleton (Hoboken) Country: United States|
|Languages: eng Pagination: 69-88 Citation Subset: IM|
|EPFL SV ISREC UPSIM, SV2.1830, Station 19, CH 1015 Lausanne, Switzerland.|
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Chromosomes, Fungal / physiology*
Cytokinesis / physiology*
Mitosis / physiology*
Schizosaccharomyces / physiology*
Journal ID (nlm-ta): Cytoskeleton (Hoboken)
Journal ID (publisher-id): cm
Publisher: John Wiley & Sons, Inc.
Copyright © 2011 Wiley-Liss, Inc., A Wiley Company
Received Day: 20 Month: 10 Year: 2010
Revision Received Day: 15 Month: 12 Year: 2010
Accepted Day: 20 Month: 12 Year: 2010
Print publication date: Month: 2 Year: 2011
Electronic publication date: Day: 10 Month: 1 Year: 2011
Volume: 68 Issue: 2
First Page: 69 Last Page: 88
PubMed Id: 21246752
|Dividing the Spoils of Growth and the Cell Cycle: The Fission Yeast as a Model for the Study of Cytokinesis|
1EPFL SV ISREC UPSIMSV2.1830, Station 19, CH 1015 Lausanne, Switzerland
2Structural Biosciences, Graduate School of Environmental and Life Sciences, University of Tsukuba1-1-1 Tennohdai, Tsukuba, Ibaraki 305-8577, Japan
|Correspondence: *Address correspondence to: Kentaro Nakano, Structural Biosciences, Graduate School of Environmental and Life Sciences, University of Tsukuba, 1-1-1 Tennohdai, Tsukuba, Ibaraki 305-8577, Japan. E-mail: email@example.com
Monitoring Editor: Makoto Kinoshita
Anupama Goyal and Masak Takaine are the joint first authors.
We will briefly introduce the S. pombe model, giving references to reviews addressing aspects of fission yeast biology that are beyond the scope of this overview. As their common name implies, cells of the fission yeast Schizosaccharomyces pombe divide by medial fission, reminiscent of cell division of animal cells. The cells take the form of a cylinder capped by hemispherical ends. During interphase, cells grow mainly at their tips, with cell length being a measure of cell cycle progression. Upon commitment to mitosis, cells stop elongating and reorganize the actin and tubulin cytoskeletons in preparation for nuclear and cell division [McCully and Robinow,1971; Mitchison and Nurse,1985; Marks et al.,1986; Hagan,1998]. The duplicated spindle pole body (SPB) inserts into the nuclear envelope [Ding et al.,1997] and the interphase microtubule array is replaced with an intranuclear spindle. Three mitotic phases have been defined [Nabeshima et al.,1998]; phase 1, when the spindle is formed and the SPBs move to opposite sides of the nucleus; phase 2, when chromosomes are captured and aligned prior to separation, during which the spindle length does not increase much; phase 3, which corresponds to anaphase B, when the sister chromatids are separated and move to opposite SPBs, which then move apart [reviewed by Hagan,1998]. The position of the division site is set by the location of the interphase nucleus and depends on a PH-domain protein mid1p and proteins that confer cell polarity [reviewed by Oliferenko et al.,2009]. A contractile ring (CR), which is composed mainly of actin and myosin filaments, is assembled at the centre of the cell during mitosis [reviewed by Pollard,2008; Pollard and Wu,2010] at the end of anaphase, the constriction of this ring is thought to guide synthesis of the septum that bisects the cell [reviewed by Ishiguro,1998; Sipiczki,2007]. Cytokinesis is mediated by CR or actin and myosin in most eukaryotic cells, including S. pombe. This has led to the use of this simple model system for studies addressing the regulatory and mechanistic aspects of cytokinesis, which have provided many insights into the regulation of this critical stage of the cell cycle. Cytokinesis is regulated by a group of protein kinases known as the septation initiation network (SIN). The SIN is essential for cytokinesis, and is coregulated with mitotic events, to ensure the coordination of mitosis and cytokinesis (see below). Table I lists the major proteins of whose function is required for cytokinesis in S. pombe. Table II lists the principal elements and regulators of the SIN, and their functions.
S. pombe has a single, essential mitotic cyclin-dependent kinase (CDK), named cdc2p: its function is conserved in distantly related yeasts such as S. cerevisiae where it is named CDC28, and in human cells, where it is known as CDK1 [Beach et al.,1982; Lee and Nurse,1987]. Cdc2p is required for mitotic entry; its activity is regulated in part by phosphorylation at Tyr15. The level of phosphorylation at this site is governed by the relative activities of the protein kinase wee1p and the phosphoprotein phosphatase cdc25p. The activities of cdc25p and wee1p are regulated at multiple levels to ensure that mitotic commitment occurs at the appropriate time; recent studies have revealed mechanisms that appear to coordinate growth, nutrient status and cell division [Petersen and Nurse,2007; Martin and Berthelot-Grosjean,2009; Moseley et al.,2009].
Reorganization of the actin and tubulin cytoskeletons for mitosis and cytokinesis depends upon commitment mitosis and CDK activity [reviewed by Marks et al.,1986; Hagan,1998]. Once mitosis has been initiated, elevated cdc2p activity prevents cytokinesis early in mitosis [Yamano et al.,1996; Chang et al.,2001; Dischinger et al.,2008]. Following CDK inactivation, cytokinesis requires the activity of a group of protein kinases known as the SIN (see below).
Unlike mammalian cells, fission yeast undergo a “closed” mitosis, in which the nuclear envelope does not break down, and the spindle forms inside the nucleus [Hagan and Hyams1988; reviewed by Hagan,1998]. A consequence of this is that the molecular mechanism controlling the positioning of the division plane differs from that in animal cells. Though microtubules are not required for cytokinesis in S. pombe [He et al.,1997,1998; Sparks et al.,1999], they do play an important role in the spatial control of the division plane. The division site corresponds to the location of the late interphase nucleus, which is kept in the middle of the cell by a microtubule-dependent mechanism [Tran et al.,2000]. Moreover, the localization of pom1p at the cell tips [Bähler and Pringle,1998] is assured by the cytoplasmic MTs in S. pombe [reviewed by Martin,2009].
The PH-domain protein mid1p, is a key factor of positioning CR at the medial cell cortex [Chang et al.,1996; Sohrmann et al.,1996; Daga and Chang,2005]. Mid1p shuttles between the nucleus and cell cortex [Paoletti and Chang,2000] and positions the division plane by acting as an “anchor” for CR proteins. At least three molecular systems control mid1p localization in a cell-cycle specific manner. The first is that cdr2p forms nodes that physically anchor a population of mid1p at cell cortex during interphase [Almonacid et al.,2009]. These interphase mid1p nodes are excluded from cell tips by pom1p and passively restricted to the medial cortex [Celton-Morizur et al.,2006; Padte et al.,2006]. This pom1p-mediated tip occlusion system is also important for controlling cell polarity [Tatebe et al.,2008]. The finding that a partial reduction of cdc15p activity is able to restore normal septum placement in cells lacking mid1 and pom1 [Huang et al.,2007] suggests that the tip occlusion system also inhibits cdc15p and other CR proteins to prevent septation at the cell ends. This is reminiscent of the situation in bacteria, where systems exist to prevent cytokinesis at the cell tips under normal conditions; reviewed by [Oliferenko et al.,2009].
The second is nuclear export of mid1p at the G2/M transition, which targets mid1p to the cortex proximal to the nucleus [Sohrmann et al.,1996; Paoletti and Chang,2000; Daga and Chang,2005], which is likely to be mediated by plo1p [Bähler et al.,1998]; Plo1p directly binds to mid1p and seems to play an important role in formation of the medial mid1p ring; the protein kinase pdk1p also contributes to this process [Bimbo et al.,2005]. Consistent with this, both kinases localize to SPB and the medial ring in mitosis [Bähler et al.,1998; Bimbo et al.,2005]. The third regulatory mechanism is thought to be the presence of domains formation of tightly packed ER in the medial region, which helps to retain mid1p at the CR [Zhang et al.,2010]. Thus, redundant mechanisms including a positive spatial cue from the centrally positioned nucleus and inhibitory signals at the cell tips contribute to medial positioning of the division plane to produce similar-sized daughter cells.
An elegant study from the Pollard lab [Wu et al.,2003] used fluorescent protein tagged ring components, which had been tested as far as possible for their biological function, to examine the kinetics and timing of CR assembly. Using SPB markers, they were able to correlate this with mitotic progression. Though the behavior of many individual CR proteins had been analyzed previously, this study examined many CR markers in parallel, under similar filming and growth conditions, enabling the relative timing of their appearance at the CR to be investigated. It therefore provides an important landmark in our understanding of how the CR assembles. The process of CR assembly and cytokinesis is shown in cartoon form in Fig. 1.
When cells enter metaphase, F-actin and myosin II (myo2p) independently appear on the medial cortex and then interact with each other to form the CR [Naqvi et al.,1999; Motegi et al.,2000]. Prior to F-actin localization, accumulation of myo2p as cortical dots is induced, probably through interaction with mid1p [Motegi et al.,2004]. Importantly, whereas full-length myo2p will only accumulate at the medial region after onset of metaphase, a C-terminal tail region of myo2p can associate with cortical mid1p nodes before the G2/M transition, suggesting that interphase-specific auto-inhibition of localization to nodes may be an immanent property of myo2p [Motegi et al.,2004]. It has also been suggested that mitosis-specific dephosphorylation of Ser1444 controls the timing of association of myo2p with cortical nodes [Motegi et al.,2004]. Though expression of the nonphosphorylatable mutant myo2S1444A induces CR-assembly in G2-arrested cells [Motegi et al.,2004], a recent study casts doubt on the importance of this phosphoregulation because the same mutation does not affect the time course of myo2p accumulation into CR, and the phosphomimetic myo2S1444D mutant, can substitute for the wild-type protein without significantly affecting cytokinesis [Sladewski et al.,2009]. At present, it remains unclear how the auto-inhibition of myo2p is relieved at G2/M transition.
In addition to myo2p, an IQGAP-like actin-crosslinking protein rng2p, the formin cdc12p, and the F-BAR protein cdc15p are also incorporated into cortical mid1p nodes in early metaphase, independently of F-actin [Wu et al.,2003]. Dynamic redistribution of actin from cell tips, where actin patches are located in interphase, to the medial region occurs during formation of CR F-actin, which depends on the actin-depolymerizing factor, adf1p [Nakano and Mabuchi,2006]. Longitudinal F-actin cables are often seen in the middle of early metaphase cells [Arai et al.,1998]. However, preexisting actin cables are not essential for CR assembly, because functional CR is formed in cells lacking the cables such as for3-null mutant [Nakano et al.,2002]. Therefore, de novo polymerization of F-actin is the dominant pathways for CR assembly in S. pombe. Actin subunits depolymerized from actin patches in cell tips are bound to profilin cdc3p [Balasubramanian et al.,1994] and are repolymerized in the medial region of the cell, probably by cdc12p [Chang et al.,1997]. The cdc12p-capped barbed end of F-actin favors the use of the cdc3p-actin complex for polymerization [Kovar et al.,2003]. Recent biochemical and genetic analyses suggest that rng2p may be involved in actin-polymerization redundantly with cdc12p [Takaine et al.,2009]. Subsequent to this, myo2p dots associate with each other through interacting with F-actin and finally the CR is formed before anaphase. Thus, the timing of CR formation in S. pombe differs from animal cells, where assembly of the CR is induced after inactivation of CDK1 and anaphase onset. Formation of the S. pombe CR early in mitosis is mediated by mid1p, which acts as an organizing scaffold for the actin polymerization machinery and myo2p to the future division site. Mid1p has a C-terminal PH domain with low similarity to the metazoan cytokinesis proteins of the anillin family, which directly bind to both F-actin and myosin II [reviewed by D'Avino,2009]. Though mid1p may share the functional similarity with anillin, it is unclear whether these proteins have evolved from a common ancestral gene.
In mid1 mutant cells, although CR formation is not initiated at metaphase, myo2p associates with a cable-like F-actin structure elongating from the cell cortex during anaphase, resulting in formation of an abnormally shaped CR, which is frequently displaced from the cell middle [Huang et al.,2007]. Therefore, mid1p-dependent events assure that S. pombe division is symmetrical while another system, probably SIN-mediated, supports CR-assembly. Interestingly, at least two other species of the Schizosaccharomyces genus, S. japonicus and S. octosporus do not have a clear ortholog of mid1p and in these organisms CR assembly is initiated during anaphase [Alfa and Hyams1990] (KN, unpublished data). All three species (KN, unpublished data) have a conserved anillin-related protein, named mid2p in S. pombe, which is required for formation of the septin ring and cell separation in S. pombe [Berlin et al.,2003; Tasto et al.,2003].
Flp1p/clp1p is the S. pombe ortholog of the conserved CDC14-family of phosphoprotein phosphatases; it is implicated in many cellular processes, and is regulated by phosphorylation and localization [Cueille et al.,2001; Trautmann et al.,2001; Wolfe et al.,2006]. During mitosis, it localizes to the CR by associating with mid1p and controls the dynamics of CR components such as cdc15p and myo2p [Clifford et al.,2008]. Flp1p/clp1p also contributes to the dephosphorylation of cdc15p, probably in cooperation with other phosphatases [Fankhauser et al.,1995; Wachtler et al.,2006; Clifford et al.,2008]. Flp1p/clp1p is likely to have many targets, and since it is not an essential gene, other phosphoprotein phosphatases will also doubtless regulate aspects of cytokinesis in S. pombe. The CR is assembled stepwise during mitosis [Wu et al.,2003]; when it is fully compacted at the onset of anaphase B, completion of cytokinesis requires the SIN. The following sections will describe the SIN, what it does and how it is regulated.
The SIN is a group of protein kinases which are essential for cytokinesis. Signaling requires the activity of three protein kinases, each of which has a regulatory subunit (kinase-regulator); cdc7p-spg1p [Fankhauser and Simanis,1994; Schmidt et al.,1997; Mehta and Gould,2006], sid1p-cdc14p [Fankhauser and Simanis,1993; Guertin et al.,2000; Guertin and McCollum,2001] and sid2p-mob1p [Sparks et al.,1999; Hou et al.,2000; Salimova et al.,2000]. SIN signaling is modulated by the nucleotide status of the GTPase spg1p [Schmidt et al.,1997; Sohrmann et al.,1998] (Fig. 2). This is determined by the balance of spontaneous nucleotide exchange, a putative GEF, etd1p [Daga et al.,2005; Garcia-Cortes and McCollum,2009] and a GAP, cdc16p [Minet et al.,1979; Fankhauser et al.,1993], with which spg1p interacts through a scaffold, byr4p [Song et al.,1996; Furge et al.,1998; Furge et al.,1999]. The SIN is also activated by the mitotic regulator plo1p [Tanaka et al.,2001], which is the fission yeast orthologue of Drosophila POLO [Ohkura et al.,1995]. Loss of SIN signaling produces multinucleate cells, while constitutive activation of the SIN results in multiseptated cells [Minet et al.,1979; Fankhauser et al.,1993; Song et al.,1996]. Ectopic activation of the SIN by either overexpression of plo1, cdc7, or spg1 promotes CR and septum formation from any stage of the cell cycle, uncoupling the usual dependency of cytokinesis upon entry into mitosis [Fankhauser and Simanis,1994; Ohkura et al.,1995; Schmidt et al.,1997; Guertin et al.,2002].
The SIN has been implicated in assembly of contractile actin ring (CR) [Hachet and Simanis,2008; Huang et al.,2008] as well as its contraction [reviewed by Gould and Simanis,1997] and the subsequent synthesis of the division septum [Jin et al.,2006]. The CR anchor mid1p and the SIN cooperate in assembly of the CR; plo1p regulates both mid1p and the SIN, which may provide global coordination of CR assembly early in mitosis [reviewed by Roberts-Galbraith and Gould,2008]; see also the discussion above. The SIN has also been implicated in reformation of the interphase microtubule array from the EMTOC at the end of mitosis [Heitz et al.,2001], formation and/or retention of astral microtubule arrays at the SPB [Krapp et al.,2001], equatorial retention of the CR during mitosis [Pardo and Nurse,2003] and in spatial reorganization of the endocytic machinery [Gachet and Hyams,2005]. The SIN may regulate the morphology network, which controls cell polarity [Kanai et al.,2005; Mendoza et al.,2005; Ray et al.,2010], thereby contributing to the switch from polar growth to CR assembly. The SIN is also implicated in the cytokinesis checkpoint, which stabilizes a defective CR to allow time to allow it to complete its assembly [Le Goff et al.,1999; Liu et al.,2000] (see below). The kinase plo1p is also required, in conjunction with the stress-response pathway, for resumption of normal growth after stress [Petersen and Hagan,2005]; in most cases, the relevant phosphorylation targets in these processes have not been determined.
Laser ablation of SPBs in fission yeast during mitosis suggests that at least one SPB must be intact during anaphase B for cytokinesis to occur [Magidson et al.,2006]. The S. pombe SPB is composed of cytoplasmic and nuclear components which are separated by the nuclear envelope and connected by fine striations [Ding et al.,1997]. The duplication of the SPB appears to be conservative [Ding et al.,1997; Grallert et al.,2004], generating “old” and “new” SPBs that can be distinguished using slow-folding RFP-tagged proteins [Grallert et al.,2004]. Studies of the localization of SIN proteins indicates that association with the SPB at various points of the cell cycle plays an important part in regulating the SIN, and therefore in the coordination of mitosis and cytokinesis [reviewed by Simanis,2003; Wolfe and Gould,2005; Krapp and Simanis,2008; Lattmann et al.,2009]. The distribution of the SIN proteins during mitosis is shown in Fig. 3.
The SIN proteins associate with the SPB via a tripartite scaffold comprised of ppc89p, sid4p and cdc11p [Chang and Gould,2000; Krapp et al.,2001; Tomlin et al.,2002; Morrell et al.,2004; Rosenberg et al.,2006]. Mutants that compromise either sid4 or cdc11 block association of SIN proteins with the SPB, and prevent SIN signaling. Ectopic activation of the SIN in a sid4 mutant fails to promote septum formation, indicating that SPB association of SIN proteins is important for signaling [Balasubramanian et al.,1998]. The scaffold proteins are seen at the SPB throughout the mitotic cycle. The requirement for the SIN in CR assembly also suggests that the SIN has a cytoplasmic role, but it is noteworthy that all of its functions seem to require the SPB-associated scaffold molecules sid4p and cdc11p [Hachet and Simanis,2008].
During interphase, spg1p, byr4p, and cdc16p are all observed at the SPB; cdc16p and byr4p are interdependent for localization [Sohrmann et al.,1998; Cerutti and Simanis,1999; Li et al.,2000]. This tripartite complex [Furge et al.,1998] is presumed to be inactive for signaling the initiation of septation, but whether it has any other role at the SPB in interphase is unclear. The steady state level of byr4p is influenced by its ability to bind spg1p [Krapp et al.,2008], which may regulate the amount of GAP present in the cell. Following CDK activation and entry into mitosis, cdc16p is removed from the SPB. In the absence of cdc16p, byr4p prevents release and hydrolysis of GTP by spg1p in vitro [Furge et al.,1998], and may thus contribute to stabilizing active spg1p in early mitosis.
Spg1p in its GTP-bound form interacts with cdc7p during mitosis [Sohrmann et al.,1998; Mehta and Gould,2006], and is observed initially on both SPBs, where low levels of byr4p are also present [Cerutti and Simanis,1999; Li et al.,2000]. Cdc7p requires spg1p to localize to the SPB [Sohrmann et al.,1998], but not vice-versa, provided byr4p is present [Krapp et al.,2008]. After the onset of anaphase B, the constellation of SIN proteins seen at the two SPBs is different. As the poles separate, the cdc7p signal at the old SPB grows fainter while the new SPB becomes brighter, reaching a maximum as the SPBs approach the cell tips [Sohrmann et al.,1998; Cerutti and Simanis,1999; Grallert et al.,2004; Garcia-Cortes and McCollum,2009]. The GAP (byr4p-cdc16p) is reconstituted first at the old SPB, and the intensity of the signals at the old SPB increase throughout anaphase [Cerutti and Simanis,1999; Li et al.,2000], mirroring the behavior of cdc7p at the new SPB. Indirect immunofluorescence has shown that byr4p becomes asymmetric before cdc7p [Cerutti and Simanis,1999]. There are ∼ 400 molecules of cdc7p at the SPB in late mitosis [Wu and Pollard,2005] and time-lapse analysis of cdc7p has shown that its removal from the new SPB correlates with closure of the CR [Garcia-Cortes and McCollum,2009].
The protein kinase sid1p and its regulatory subunit cdc14p appear at the new SPB only after the inactivation of CDK and onset of anaphase B [Guertin et al.,2000; Dischinger et al.,2008]. Like cdc7p, the signal increases in intensity during anaphase B spindle elongation, peaking as the SPBs approach maximal separation. Sid1p and cdc14p are interdependent for localization to the SPB, which also requires functional spg1 and cdc7 [Guertin et al.,2000]. Sid2p and mob1p are also interdependent for localization and associate with both SPBs throughout mitosis, and also with the medial region at the time of septum formation. The sid2p-mob1p complex requires functional SIN and CR components to localize to the medial region [Sparks et al.,1999; Hou et al.,2000; Salimova et al.,2000]. Full activation of sid2p also requires functional cdc7p [Sparks et al.,1999]. Sid2p and mob1p localization to the SPB is reduced in cdc7 mutants and some alleles of spg1 [Sparks et al.,1999; Hou et al.,2000; Salimova et al.,2000].
Biochemical analysis has shown that cdc16p, spg1p, mob1p, and cdc13p (the mitotic cyclin for cdc2p) all bind to the N-terminal domain of cdc11p [Morrell et al.,2004]. Maintaining the association of cdc7p and sid2p with the SPB in anaphase B requires etd1p function [Daga et al.,2005]. Studies of the localization and activity of sid2p have given rise to a model placing it downstream of cdc7p and sid1p [Sparks et al.,1999; Guertin et al.,2000]. However, given its symmetrical distribution during anaphase, it cannot be excluded that it plays different roles at the new and old SPBs. Immunoelectron microscopy has shown that in interphase, sid2p is associated with the cytoplasmic face of the SPB [Sparks et al.,1999]. It is not known whether the other SIN proteins also localize to the outer face of the SPB during mitosis. Taken together, these data have led to the idea that the order of action of the SIN proteins is cdc7p-spg1p, then sid1p-cdc14p, and finally sid2p-mob1p [Guertin et al.,2000].
The transition from the symmetric to the asymmetric configuration of the SIN and the initiation of septation requires inactivation of mitotic CDK [Yamano et al.,1996; He et al.,1997; Guertin et al.,2000; Chang et al.,2001; Dischinger et al.,2008]. It has been proposed that this asymmetric distribution of proteins is important to turn off the SIN and complete cytokinesis [Garcia-Cortes and McCollum,2009; reviewed by Lattmann et al.,2009]. Consistent with this, cells in which the GAP is absent, leading to permanent activation of spg1p, show a symmetric distribution of SIN proteins during anaphase [Sohrmann et al.,1998; Guertin et al.,2000], and undergo multiple rounds of septation without cleavage [Minet et al.,1979; Song et al.,1996]. The transition to the asymmetric state of the SIN is also influenced by chromosome segregation [Mayer et al.,2006]; cells that contain lagging chromosomes on an elongating spindle show symmetric distribution of cdc7p; the nature of the signaling pathway involved is unknown, but probably differs from that regulating the association of mad2p with the SPB [Mayer et al.,2006]. Mutation of either par1, the B′ regulatory subunit of PP2A [Jiang and Hallberg,2001], or the regulator of mitotic commitment fin1 [Grallert et al.,2004], result in an increase of the number of cells in which cdc7p segregates symmetrically during anaphase. In cells arrested by the cytokinesis checkpoint, cdc7p remains associated with the new SPB as long as the defective CR is present in the cell [Mishra et al.,2004], consistent with signaling between the CR and SPB. Loss of the phosphoprotein phosphatase flp1p/clp1p affects maintenance of cdc7p at the new SPB in cytokinesis-checkpoint arrested cells [Mishra et al.,2004], and also impedes recruitment of sid1p to the new SPB in late anaphase [Trautmann et al.,2001]. Inactivation of etd1p results in premature loss of cdc7p from the SPBs in anaphase [Daga et al.,2005], while excess etd1p delays removal of cdc7p from the new SPB after cell separation [Garcia-Cortes and McCollum,2009], leading to the proposal that a feedback mechanism regulates SIN activity; reviewed by [Lattmann et al.,2009].
A number of putative regulators of the SIN have been identified genetically; zfs1 and scw1 are RNA binding proteins [Beltraminelli et al.,1999; Karagiannis et al.,2002; Jin and McCollum,2003; Cuthbertson et al.,2008], but the RNAs involved in SIN regulation remain undefined. The nucleolar protein dnt1p [Jin et al.,2007] and the phosphatases PP2A [Jiang and Hallberg,2001; Le Goff et al.,2001] and flp1p/clp1p [Cueille et al.,2001; Trautmann et al.,2001] have also been identified as regulators of the SIN, though their targets remain unknown. Fully active cdc2p inhibits the SIN early in mitosis and its inactivation is required for septum formation [Yamano et al.,1996; He et al.,1997; Chang et al.,2001; Dischinger et al.,2008]; the association of cdc13p with cdc11p may facilitate this regulation [Morrell et al.,2004]. Furthermore, cdc2p and the SIN may cooperate to regulate septation in interphase [Cerutti and Simanis,1999]. Proteolysis also plays a role in regulating the SIN; resetting the SIN involves the APC/C subunit nuc2p [Chew and Balasubramanian,2008] and elimination of etd1p [Daga et al.,2005; Garcia-Cortes and McCollum,2009]. The putative ubiquitin ligase dma1p is an inhibitor of the SIN which is required to prevent septum formation in mitotically arrested cells [Murone and Simanis,1996]; it influences recruitment of plo1p to the SPB and its ubiquitin ligase domain is required for its function [Guertin et al.,2002]. The protein kinase fin1p requires the SIN for its localization to the SPB, and it modulates SIN signaling [Grallert et al.,2004], which may point to the existence of feedback regulation of the SIN. In this context it is also noteworthy that plo1p is recruited to the SPB prematurely in a cdc7 mutant at the permissive temperature [Mulvihill et al.,1999]. Finally, it has been proposed that to coordinate mitotic progression and cytokinesis, the γ-tubulin complex inhibits the SIN until mitotic CDK is inactivated [Vardy et al.,2002].
The biological counterpart of the S. pombe SIN in another yeast, Saccharomyces cerevisiae, is called the mitotic exit network (MEN). In addition to a role in cytokinesis, the MEN is required for the inactivation of CDK, and exit from the mitotic state into G1; for reviews, see [Burke,2009; Rock and Amon,2009]. Many components are conserved structurally (and in some cases, also to the level of functional cross-complementation) between the MEN and SIN [for details see the following reviews: Bardin and Amon,2001; Simanis,2003; Stegmeier and Amon,2004]. Some components of the SIN have recognisable counterparts in higher eukaryotes; for example, the SIN scaffold cdc11p shares a common domain with centriolin, which is required for cytokinesis [Gromley et al.,2003; Gromley et al.,2005]. The kinase sid2p-mob1p is a member of the NDR kinase family, which is implicated in growth control and cytokinesis in multicellular eukaryotes as part of the Salvador-Warts-Hippo tumor suppressor network. In this context, it seems to function by inhibiting gene expression programs; it is unclear whether the SIN has any role in regulating gene expression [reviewed by Harvey and Tapon,2007; Matallanas et al.,2008; Hergovich and Hemmings,2009; Zhang et al.,2009].
As mentioned above, the SIN seems to be important for stabilizing the CR after onset of anaphase and to sustain assembly of CR components until cytokinesis is finished. The SIN and flp1p/clp1p, are both implicated in a cytokinesis checkpoint, which blocks the next round of mitosis in response to perturbed assembly of the CR [Le Goff et al.,1999; Cueille et al.,2001; Trautmann et al.,2001; Mishra et al.,2004]. Flp1p/clp1p is sequestered in the nucleolus during interphase and is released to the nucleoplasm and then the cytoplasm during mitosis. The core SIN kinase sid2p phosphorylates the flp1p/clp1p to keep it in the cytoplasm, which contributes to the function of the cytokinesis checkpoint [Chen et al.,2008a].
Overexpression of C-terminal truncated cdc12p, probably corresponding to a dominant active form lacking the auto-inhibitory domain, induces cdc15p- and CR-dependent cytokinesis even in interphase cells [Yonetani and Chang,2010]. Overexpression of cdc15p is able to induce actin rearrangements to the medial region in G2-arrested cells. Cdc15p may be negatively regulated by phosphorylation in interphase [Fankhauser et al.,1995]. Cdc15p can self-assemble and may interact directly with the plasma membrane through its F-BAR domain [Roberts-Galbraith et al.,2010]. Dephosphorylation of cdc15p promotes its oligomerization and increases its affinity for one its binding partners, cdc12p [Roberts-Galbraith et al.,2010]. In view of the fact that cdc12p physically associates with cdc15p [Carnahan and Gould,2003], high doses of these proteins may be possible to induce actin-polymerization beneath cell cortex and ectopic CR assembly bypassing mitosis-specific regulation including phosphorylation. Ectopic activation of the SIN in interphase will also promote CR assembly and septum formation [Schmidt et al.,1997], bypassing the mid1p spatial cue [Hachet and Simanis,2008].
Though whole genome-based screening shows that more than 200 proteins are localized to the division site in S. pombe, only a small subset of these can trigger reorganization of F-actin, CR formation and septation when their activity is altered [Matsuyama et al.,2006; reviewed by Bathe and Chang,2010]. These may define rate-limiting steps or control points in CR assembly analogous to the pivotal role played by the rhoA GTPase in animal-cell cytokinesis (see below).
After the completion of nuclear division, the CR constricts, which is followed by the primary septum synthesis. At present, it is unclear whether CR constriction is an active, motor-driven process, or whether it occurs passively, as the septum is deposited behind it. Previous studies have shown the following: Mutant cells that are unable to assemble a coherent CR deposit septum materials at the cell cortex [Streiblova et al.,1984; Marks et al.,1992], which suggests that the septum cannot close without constriction of the CR. In a spheroplast, where cell wall synthesis is impaired the CR does not constrict [Jochová et al.,1991], though it should be noted that it is not known whether all the required proteins are present in these CRs. Mutant cells that lack bgs1p/cps1p, the β-glucan synthase required for synthesis of the division septum, retain the CR with no constriction for several hours at the restrictive temperature [Liu et al.,2000]. This may indicate that septum synthesis is required for CR constriction; however, since this arrest is maintained by a checkpoint [Le Goff et al.,1999; Liu et al.,2000] and the mechanisms underpinning the checkpoint are incompletely understood, other interpretations are possible. Furthermore, the mechanism by which expansion of plasma membrane occurs at the division site remains poorly understood. Although exocytotic machineries such as the exocyst complex and the presumed vesicle transporter myo52p (myosin V) accumulate at the division site, neither CR constriction nor septum formation is interrupted in mutants lacking these functions [Motegi et al.,2002; Wang et al.,2002; Mulvihill et al.,2006]. However, the Golgi-mediated secretory pathway seems to be required for medial localization of bgs1p/cps1p [Liu et al.,2002]. Future studies should determine whether membrane ingression, CR constriction and septation are actively coordinated.
As the primary septum is synthesized, actin patches accumulate around the region of septation. In S. pombe, the Arp2/3-complex is not required for CR assembly [Wu et al.,2006], but is essential for formation of actin patches [McCollum et al.,1996]. Loss of the Arp2/3-complex function reduces the rate of CR constriction [Wu et al.,2006] without impairing the deposition of septal material [McCollum et al.,1996]. Since actin patches are the structure responsible for endocytosis [Gachet and Hyams,2005], it is possible that endocytosis is involved in membrane ingression at the division site and/or septation. This idea is supported by findings that mutants defective in endocytosis frequently form an abnormal septum [Castagnetti et al.,2005; Ge et al.,2005]. Interestingly, it has recently been demonstrated that endocytosis restricts the membrane domain required for localization of the exocytosis machinery to the division plane during cytokinesis of the higher plant Araidopsis thaliana [Boutte et al.,2010]. Moreover, Rab11-dependent membrane recycling between the plasma membrane and endosomes seems to recruit signaling molecules inducing furrow ingression at the cleavage site in the Drosophila early embryo [Cao et al.,2008]. Coincidently, in S. pombe cells the Rab11-homolog ypt3p localizes to the medial region during cytokinesis, dependent on an intact actin cytoskeleton [Cheng et al.,2002]. Therefore, it is possible that endocytosis and membrane recycling may also function in cell cleavage in this S. pombe.
The primary septum is composed of linear chains of 1,3-β-glucan [Humbel et al.,2001]. After completion of the primary septum synthesis, the secondary septum, which becomes the cell wall of the new end of the daughter cell, is synthesized on both sides of the primary septum. Finally, cell separation is induced by enzymatic degradation of the primary septum by glucanases such as the endo β-1,3-glucanase, eng1p, and endo-α-glucanase, agn1p [Martin-Cuadrado et al.,2005]. Mutations defective in either glucanase activity or extracellular secretion of the enzymes result in highly elongated and multicompartmented cells (chains of cells, each containing one nucleus, separated by an uncleaved septum). The transcription factor ace2p controls a late-cell-cycle specific gene expression program, which is required for cell separation; deletion of ace2 produces multicompartmented cells [Alonso-Nunez et al.,2005; Petit et al.,2005].
In this section, we will discuss the assembly, constriction and disassembly of the CR, with particular emphasis on the mechanical and structural aspects of these processes. We will also compare the properties of the S. pombe CR with those of mammalian cells, and speculate upon possible mechanisms for its assembly and constriction. We will begin with a brief review of the mechanics of cytokinesis in mammalian cells.
In animal cells, cytokinesis is brought about by membrane ingression, which has been named the cleavage furrow (CF). The CF is thought to be induced by geometrical asymmetry of the cortical tension in the cell. Several mechanisms for CF formation have been proposed [reviewed by Wang,2005]; currently, the most favored one is the purse-string model [reviewed by Mabuchi and Itoh,1992; Noguchi et al.,2001; Pollard,2010]. The equatorial CR is composed of F-actin filaments and myosin II, and their interaction produces the force required for membrane ingression at the site of division. The concentration of F-actin at the CR seems to be particularly evident in nonmotile cells such as early embryos or yeasts. Though the F-actin at the CR is often parallel to the equator of the cell, there are also examples where cortical F-actin or myosin II are observed perpendicular to the division plane in some dividing cells [Fishkind and Wang,1993; DeBiasio et al.,1996; Oegema et al.,2000; Murthy and Wadsworth,2005; Chen et al.,2008b]. According to the purse-string model, these cortical actomyosin filaments should not contribute to constriction of the ring. Moreover, there are some cell types, especially those which are adherent to a substrate, which are able to divide without using a CR [Neujahr et al.,1997; O'Connell et al.,2001; Kanada et al.,2005]; in these cases, it seems that coordination of the compression of the equatorial cortex and cortical expansion at the cell poles is sufficient to induce a CF. Globally, it is likely that these mechanisms are not mutually exclusive but interdependent, and the extent to which each of them contributes to CF ingression differs according to the cell type. Thus, though cytokinesis is a fundamental cellular event, the mechanism that brings it about in any given cell-type will be a mixture of conserved and cell-type-specific features.
In animal cells, the central spindle and overlap region of astral microtubules (MTs), which extend from opposite spindle poles, promote CR assembly at telophase. Centralspindlin, a protein complex consisting of MKLP1, a kinesin-6 dimer, and Rho-family GTPase-activating protein (RhoGAP) subunits, plays the central role in this system [Mishima et al.,2002]. Cell cycle-dependent kinase 1 (CDK1), which promotes mitotic events such as centriole duplication, chromosome condensation, and spindle formation, phosphorylates MKLP1 during metaphase, which prevents it from interacting with MTs [Mishima et al.,2004]. After CDK1 is inactivated at the onset of anaphase, the protein-phosphatase CDC14 dephosphorylates MKLP1, and Centralspindlin moves on MTs and accumulates at their equatorial plus-ends. The POLO-like kinase, which regulates multiple mitotic events in addition to cytokinesis, induces association of ECT2, a guanine nucleotide-exchange factor for Rho GTPase, with Centralspindlin and localizes this protein complex to the equatorial region of the anaphase cell [reviewed by Petronczki et al.,2008; Wolfe et al.,2009]. As a result, Rho is specifically activated there and induces CR formation by promoting actin-polymerization and activation of myosin II via effectors such as formin and Rho-kinase. Furthermore, in the equatorial region of Caenorhabditis elegans oocyte Centralspindlin also reduces Rac GTPase-activity, which inhibits the formation of an Arp2/3-complex-dependent branched actin network and thereby ensures formation of the formin-dependent CR, which is composed of straight F-actin [Canman et al.,2008]. In addition to this, the tips of astral MTs which contact the cell poles relax cortical tension at the polar regions, which leads to a relative increase in equatorial contractility in C. elegans oocyte [reviewed by Werner and Glotzer,2008].
Cytokinesis is accomplished by the scission of a “bridge” connecting the daughter cells. Dynamic reorganization of membranes including scrambling of outer and inner sides of plasma membrane, SNARE–mediated vesicle fusions, and membrane scission by ESCRT complex is required for this step [reviewed by Prekeris and Gould,2008]. Vesicle fusion is particularly important for cytokinesis in higher plant cells where formation of the cell plate progresses centrifugally [reviewed by Jurgens,2005; Otegui et al.,2005; Dhonukshe et al.,2007]. Interestingly, an archaeal ortholog of Vps4, a protein stimulating ESCRT-mediated membrane scission, is required for cell division in the crenarchaeon Sulfolobus acidocaldarius [Lindas et al.,2008]. Therefore, it is possible that some molecular systems in cytokinesis may be conserved across evolutionary kingdoms; alternatively, their mechanistic similarity may reflect convergent evolution. Future study of the molecular basis for cytokinesis in various cells and organisms will doubtless help to answer this question.
In this section, we will address two questions: first, what is the origin of CR F-actin? Second, is the CR formed by a spot/leading cable mechanism, or from a band of nodes? Considerable effort has been devoted to analysis of CR assembly [Vavylonis et al.,2008; Yonetani et al.,2008; Coffman et al.,2009]; reviewed by [Mishra and Oliferenko,2008; Roberts-Galbraith and Gould,2008; Bathe and Chang,2010; Pollard and Wu,2010]. These studies have given rise to two models for the initial assembly of CR F-actin in fission yeast. One is the node model, which assumes that short F-actin filaments are nucleated in random directions from about 65 nodes, each of which contains two cdc12p dimers [Wu and Pollard,2005], and then condensed into a continuous ring by a search, capture, pull and release (SCPR) mechanism that is driven by myosin II motor activity [Wu et al.,2006; Pollard,2008; Vavylonis et al.,2008; Pollard and Wu,2010]. The other is the spot model, which proposes that F-actin cables emanating from a single or several spot(s) of clustered cdc12p encircle the cell equator to form a ring [Chang et al.,1997; Chang,1999; Arai and Mabuchi,2002; Wong et al.,2002; Carnahan and Gould,2003; Motegi et al.,2004; Kamasaki et al.,2007]. These two models are consistent in that they agree that CR F-actin is polymerized de novo at mitosis (and does not arise from conversion of interphase actin cables or patches), but they are differ significantly with regard to how CR F-actin is formed: from dozens of cdc12p nodes or from a small number of cdc12p spots. Recent studies have shown that the cdc12p spot formation depends on its FH3 domain and the actin-bundling protein ain1p, and is dispensable for CR assembly [Yonetani et al.,2008; Coffman et al.,2009]. Thus, it is likely that recruitment of cdc12p to the medial region and concomitant initial CR F-actin assembly may be mediated through multiple distinct mechanisms operating individually or in parallel, reminiscent of the situation in mammalian cells, where multiple redundant mechanisms also operate (see above). Coffman et al. found that cdc12p appears in, at least, four distinct forms: speckle (one cdc12p dimer), node (two cdc12p dimers), spot (a probable cluster of cdc12p dimers) and ring [Coffman et al.,2009]. It is possible that the abundance of each form is dictated by the extent of aggregation of cdc12p. Analysis of how oligomerization of cdc12p affects its actin polymerization activity may help to elucidate the way in which multiple modes of initial CR F-actin assembly vary.
At least two nonexclusive mechanisms seem to be involved in recruitment of actin to the equatorial region during cytokinesis in animal cells: cortical flow and de novo assembly. The cortical flow of preformed F-actin is supported by direct observations of flux of fluorescently labeled actin [Cao and Wang,1990; Chen et al.,2008b] or GFP-actin [Zhou and Wang,2008] toward the CF. Although mechanism of the cortical flow remains elusive, the actin flux is suppressed by myosin II specific inhibitor blebbistatin, suggesting that myosin II motor is involved in these processes. The de novo assembly of CR F-actin was observed as accumulation of actin at the equator of blebbistatin-treated mitotic cells where the cortical flow is abolished [Guha et al.,2005; Murthy and Wadsworth,2005; Zhou and Wang,2008]. Involvement of formins that fascilitate actin assembly in cytokinesis also supports this hypothesis [Severson et al.,2002; Watanabe et al.,2008].
It is generally accepted that the CR is comprised mainly of actin and myosin II. However, their precise configuration in the ring remains undetermined. EM observations in several dividing cells have revealed that CR F-actin generally aligns parallel with the equator beneath the plasma membrane at the division site [Schroeder,1972; Sanger and Sanger,1980; Yasuda et al.,1980; Maupin and Pollard,1986; Kanbe et al.,1989; Kamasaki et al.,2007]. These filaments are often composed of many small bundles in series, each of which has an average length of 0.6 μm in S. pombe cells. The CR actin filaments have mixed polarities, and interdigitating myosin-like thick filaments between them were also observed in animal cells [Sanger and Sanger,1980; Maupin and Pollard,1986]. Based on these observations, the purse-string model is favored as the mechanism for constriction of CR [Schroeder,1972; Mabuchi and Itoh,1992; Satterwhite and Pollard,1992]. This model assumes that sliding of anti-parallel F-actin via interaction with myosin II filaments shortens the unitary bundles of CR, like the contraction of muscle sarcomeres, and hence drive shrinkage of the ring. The validity of this model in S. pombe is discussed below.
As mentioned above, cortical F-actin filaments oriented perpendicular to CR, which would not be involved in CR constriction according to the purse-string model, are often detectable. Filaments with this orientation have escaped detection by EM observation. Given the high turnover rates of actin and myosin II in CR, this perpendicular F-actin may also be dynamic, probably more than CR F-actin, and hence may be difficult to preserve during severe fixation. Functional dissection of these filaments might substantiate alternative mechanisms for cortical ingression during cytokinesis [Wang,2005; Eggert et al.,2006]. Along similar lines, it should also be noted that a measurable amount of short F-actin filaments orthogonally crossing the CR F-actin were detected in dividing fission yeast cells [Kamasaki et al.,2007].
Some actin-binding proteins (ABPs) localized selectively at CR are thought to characterize the special properties of CR F-actin bundles. The actin-bundling protein α-actinin localizes to the CF in dividing NRK cells and is involved in accumulation of CR F-actin [Mukhina et al.,2007]; Another actin-bundling protein EPLIN also locates to the CF during cytokinesis in HeLa cells and regulates local accumulation of active myosin II [Chircop et al.,2009]; IQGAP proteins accumulate in CF regions of dividing sea urchin eggs [Nishimura and Mabuchi,2003] and mouse oocyte [Bielak-Zmijewska et al.,2008] and might be involved in cytokinesis. Anillin also bundles F-actin and localizes to CR in Drosophila and HeLa cells [Field and Alberts,1995; Straight et al.,2005]. In fission yeast cells, actin-bundling proteins including α-actinin ain1p, fimbrin fim1p, the calponin-like stg1p, and the IQGAP rng2p localize to the CR and affect the organization of CR F-actin [Eng et al.,1998; Nakano et al.,2001; Wu et al.,2003; Nakano et al.,2005; Takaine et al.,2009].
It is noteworthy that the equatorial accumulation of F-actin is not always evident in dividing cells, whereas ABPs or myosin II are clearly detectable in most cases [e.g., Neujahr et al.,1997; Foe and von Dassow,2008; Watanabe et al.,2008]. In fission yeast, the N-terminal head (actin-binding) domain of myosin II localizes by itself specifically to CR F-actin, but not to F-actin patches or cables [Lord et al.,2005]. Moreover, overexpression of rng2p induces formation of F-actin bundles associated with myo2p (MT and KN, unpublished data). Therefore, myosin II proteins may be tethered to the CR F-actin through the specific protein interactions, not simply because of the high concentration of F-actin. Although anillin interacts directly with myosin II, its depletion barely affects the CR localization of myosin II [Straight et al.,2005]. Similarly, even in the absence of mid1p, myo2p localizes only to CR F-actin in fission yeast [Motegi et al.,2004]. Biochemical examination of the interactions between myosin II and F-actin network or bundles induced by these proteins should elucidate the nature of specific targeting of myosin II to CR F-actin.
It also remains possible that myosin II contributes to organization of CR F-actin bundles. Myosin II is implicated in rearrangement of the actin cytoskeleton in protruding lamellae of fibroblast cells [Verkhovsky et al.,1995]. Myosin II filaments are also involved in assembly of stress fibers [Hotulainen and Lappalainen,2006] and confer contractility upon them. In particular, it is of great interest that active myosin II motors induce reorganization of F-actin into various patterns only in collaboration with actin-bundling proteins [Backouche et al.,2006]. In these systems myosin II is thought to act as an active F-actin crosslinkers, which can generate force between filaments using the energy of ATP hydrolysis, whereas so-called actin-bundling proteins act as passive crosslinkers and do not produce any work. Thus self-organization of F-actin induced by both active and passive crosslinkers might contribute to CR formation in fission yeast, which is partially conceptualized in the search, capture, pull and release (SCPR) model. Future studies will doubtless test this hypothesis.
In the purse-string hypothesis, myosin II motors are presumed to generate a force driving CR constriction via interaction with CR F-actin. Inhibition of the ATPase activity of myosin II using blebbistatin blocks cytokinesis in mammalian cells without affecting CR F-actin assembly [Straight et al.,2003]. Interestingly, studies using blebbistatin also revealed that myosin II is involved in turnover of CR F-actin [Guha et al.,2005; Murthy and Wadsworth,2005].
S. pombe has two myosin II isoforms, myo2p and myo3p (also called myp2p), both of which localize to the CR [Bezanilla and Pollard,2000]. Myo2p is essential for cytokinesis, while myo3p is required for growth under stress conditions. Localization of the myosins to cortical nodes and the CR has been analyzed extensively [Naqvi et al.,1999; Motegi et al.,2000; Mulvihill et al.,2001; Wu et al.,2003; Motegi et al.,2004; Martin-Garcia and Valdivieso,2006; Sladewski et al.,2009]. The precise function of myosin II in S. pombe cytokinesis remains unclear. F-actin accumulates at the division site in myo2-null cells but fails to form a ring [Kitayama et al.,1997]. Biochemical experiments using purified myo2p revealed that a G345R mutation (the temperature-sensitive myo2-E1 allele), significantly reduces the actin-binding and motor activity of myo2p [Lord and Pollard,2004]. In the myo2-E1 mutant cells, node condensation into a ring abolished at restrictive temperature and is delayed at the permissive temperature [Coffman et al.,2009]. Moreover, CRs in myo2-E1 cells constrict twofold slower than those in wild-type cells [Stark et al.,2010]. These observations are consistent with the SCPR model in that myosin II functions both in assembly of the F-actin ring and contraction of the CR. Myo3p does not appear as an equatorial band of nodes in early mitosis and joins the CR after myo2p has formed a ring [Wu et al.,2003]; this may indicate that myo3p plays an important role in CR constriction. Alternatively, since myo3p associates physically with chitin-synthase, it may contribute to CR closure via septum formation [Martin-Garcia and Valdivieso,2006]. Since a null-mutation of myo3 exacerbates the phenotype of myo2-E1 cells, the two myosin-IIs seem to share overlapping functions in cytokinesis [Motegi et al.,2000].
Folding of the myosin head domain requires a co-chaperone of the (UNC-45/CRO1/She4p) family of proteins. In C. elegans, UNC-45 colocalizes with myosin II during cytokinesis in the early embryos [Barral et al.,2002; Kachur et al.,2004] and is required for assembling thick filaments of myosin II in sarcomeres [reviewed by Kachur and Pilgrim,2008]. S. pombe rng3p belongs to the same UCS -family and associates with myo2 and other four myosin proteins cotranslationally [Amorim and Mata,2009]. Rng3p is involved in CR formation cooperatively with myo2p [Wong et al.,2000] and promotes motor activity of myo2p for F-actin [Lord and Pollard,2004; Lord et al.,2008]. Rng3p localizes to the CR just before CR constriction in wild-type cells [Lord and Pollard,2004], suggesting that rng3p may induce myo2p-dependent CR constriction. Interestingly, rng3p is concentrated in nodes at metaphase in myo2-E1 cells [Lord et al.,2008].
One of the observable characteristics of myosin II molecules is to assemble into bipolar thick filaments through their tails [Kaminer and Bell,1966]. When considering the role of myosin II in cytokinesis, its filamentogenesis should be examined because the bipolar filaments are indispensable prerequisite for CR constriction according to the purse-string model. In dividing Dictyostelium or Drosophila S2 cells, accumulation of individual myosin-II filaments at the equatorial region has been visualized as small rods less than 1 μm in length by fluorescence microscopy [Yumura and Fukui,1985; Yumura et al.,2008; Vale et al.,2009]. To date, no such myosin-II-containing rod-shaped structures have been observed in fission yeast cells. Biochemical studies have revealed that both myo2p purified from fission yeast cells and bacterially expressed myo3p tail are insoluble at physiological salt concentrations and become soluble in high salts like common myosin-IIs [Bezanilla and Pollard,2000; Lord and Pollard,2004]. Quantitative microscopic analysis estimated that about 40 molecules of myo2p are present in each cortical node, so the local concentration of myo2p in CR would be 20 μM [Wu and Pollard,2005], which both seems to be enough to form thick filaments. However, it is still unknown whether these myosin-IIs form ordered bipolar filaments in each node or in CR. In this context, it will be important to investigate whether the rng3p has an ability to induce oligomerization of myo2p.
FRAP analysis has shown that CR F-actin and cortical F-actin turn over rapidly both in fission yeast and mammalian cells [Pelham and Chang,2002; Guha et al.,2005; Murthy and Wadsworth,2005]. The actin-depolymerizing factor (ADF)/cofilin-family (hereafter refer to as ADF) proteins facilitate depolymerization and severing of actin filaments and hence play a key role in regulation of F-actin dynamics in various motile processes; reviewed by [Pantaloni et al.,2001]. In some animal cells, ADF proteins are required for completion of cytokinesis, but not for assembly of the CR [Gunsalus et al.,1995; Somma et al.,2002; Kaji et al.,2003; Ono et al.,2003]. It is likely that these ADFs contribute to turnover of CR F-actin or its active disassembly.
In S. pombe cells, the sole ADF, named as adf1p, localizes to the CR and is essential for accumulation of F-actin at the division site during cytokinesis [Nakano and Mabuchi,2006]. This is consistent with the observation that Xenopus ADF/cofilin, XAC, localizes to the leading edge of the CF in a fertilized egg and also participates in its formation [Abe et al.,1996]. Complementation-assays in fission yeast using mutant ADFs suggest that the actin-severing activity of adf1p may primarily contribute to its function in cytokinesis rather than its actin-depolymerizing activity. Actin-severing increases number of filament ends, which is required to induce dynamic turnover of actin subunits, since internal subunits are never exchanged in actin filaments. Andrianantoandro and Pollard, however, revealed that high concentration of adf1p nucleates actin polymerization whereas it effectively severs F-actin at lower concentrations [Andrianantoandro and Pollard,2006]. Thus, in fission yeast, adf1p would promote turnover of CR F-actin by a combination of its actin-severing and -nucleation activities. Another F-BAR protein, imp2p and a paxillin-related protein, pxl1p may also be implicated in CR disassembly or constriction [Demeter and Sazer,1998; Ge et al.,2005; Pinar et al.,2008], though their mechanism of action in this context remains unclear.
It is unequivocal that in dividing animal cells net inward forces are generated along the equator, whether by the CR or by other mechanisms, and they drive the constriction of the medial cortex [Rappaport,1967; Hiramoto,1975]. On the other hand, contribution of CR to the generation of contractile force is elusive in fission yeast as discussed above. In the budding yeast, S. cerevisiae, the CR is not essential for cytokinesis, and septation alone manages to carry out the closure of bud neck [Bi et al.,1998]. The SIN pathway is not only required for localization of β-1,3-glucan synthase, bgs1p, at the division plane for formation of the primary septum [Liu et al.,2002], but is also essential for maturation of CR [Hachet and Simanis,2008]. Hyperactivation of the SIN pathway induces ectopic F-actin ring formation [Schmidt et al.,1997]. Taken together, CR constriction and septation would be interdependent in both mechanical and signaling aspects, and it may be difficult to distinguish separately their functions in cytokinesis. We believe, however, that fission yeast CR shares enough functional molecular bases with those of animal cells to serve as a model system.
Whatever the actual function of CR constriction is, its mechanism(s) is still an open question. As discussed above, the purse-string model should be challenged by examining whether myo2p assembles into minifilaments in vitro. Fine and time-resolved EM observation of CR and the medial region of dividing fission yeast cells may also help to address this issue. An attractive model for generation of the contractile force has been proposed, which posits that polymerization and depolymerization of CR F-actin can produce mechanical force for the ring contraction in the presence of end-tracking crosslinkers even without myosin II motors [Zumdieck et al.,2007]. In this model, tracking of a depolymerizing filament end by the crosslinker, which also binds to the second filament, is harnessed to generate sliding force between the two filaments. At present, the model remains to be validated, but it clearly seems worth pursuing, given the general and critical importance of both ADFs and formin proteins in cytokinesis.
The fission yeast Schizosaccharomyces pombe has proved to be an informative model for the study of cytokinesis and its coordination with mitosis. Many of the structural components required for cytokinesis are well conserved through evolution, so the fission yeast provides an excellent background in which to test the in vivo effects of defined mutations; when proteins are involved in multiple processes, hypomorphic alleles may permit separation of these functions. Though we have learnt a great deal about how cytokinesis occurs in S. pombe through a judicious mixture of cell biology, genetics and biochemical analysis, it is clear from the foregoing discussion that much remains to be done. Scientifically speaking, the next few years should be very exciting!
Research in the Simanis lab is supported by grants from the Swiss National Science Foundation and EPFL. MT and KN are supported by a Grant-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science, and Technology (MEXT; No. 22019003).
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[Figure ID: fig01]
Fission yeast cytokinesis
The cartoon shows the various stages of CR formation with respect to mitotic progression. See text for details.
[Figure ID: fig02]
Components of the SIN
The cartoon depicts the core components of the SIN and the presumed relationship between them. For the sake of clarity, nonessential regulators are not shown. See text for additional details.
[Figure ID: fig03]
Localization of SIN proteins during interphase and mitosis
The cartoon depicts the localization of the core SIN proteins during mitosis and cytokinesis. The size of the circles associated with the SPB is meant to represent the intensity of the signal that is observed. For the sake of clarity, the localization of regulatory proteins is not shown: see Lattmann et al. ; Simanis  for additional details.
Proteins Required for Cytokinesis in S. pombe
|mid1p/dmf1p||PH-domain protein||Shuttles between nucleus and cytoplasm and determines the division site|
|plo1p||Polo-like Ser/Thr protein kinase||Induces exclusion of Mid1p from nucleus and activates SIN pathway|
|act1p||Conventional actin||Major component of CR|
|myo2p||Myosin II heavy chain (MHC II)||Actin-based motor activity, essential for cytokinesis|
|myo3p/myp2p||Unconventional MHC II||Actin-based motor activity, essential for cytokinesis under stressful condition|
|cdc4p||EF-hand protein||Essential light chain of myosin II, associating with rng2p and pik1p|
|rlc1p||EF-hand protein||Regulatory light chain of myosin II, phosphoregulated by pak1p|
|rng2p||IQGAP-like protein||F-actin-crosslinking, actin polymerization, controlling myo2p distribution|
|cdc12p||Formin||Induces actin polymerization from G-actin-cdc3p (profilin) complex|
|cdc15p||PCH-family, F-BAR-domain||Controls membrane domain and binds to cdc12p and myo1p|
|ain1p||α-actinin||Crosslinks F-actin, essential for cytokinesis under stressful condition|
|fim1p||Fimbrin||F-actin-bundling, unessential for CR formation|
|adf1p||ADF/cofilin||Accelerates actin-depolymerization and severs F-actin|
|cdc8p||Tropomyosin||Activates actin-myosin II interaction, protects F-actin from Adf1|
|rng3p||UCS-family protein||Activates motor activity of myosin II|
|cps1p/drc1p||β-1,3-glucan synthase||Septum synthesis, a possible sensor for cytokinesis checkpoint signaling|
|mok1p||α-1,3-glucan synthase||Septum synthesis|
|eng1p||Endo-β-1,3-glucanase||Required for cell separation probably by digesting the primary septum|
|agn1p||Endo-α-glucanase||Required for cell separation redundantly with eng1p|
|mid2p||Similar to Mid1p||Localizes septin ring at a division site, required for cell separation|
|ace2p||Zinc finger C2H2 type domain||Induces expression of genes required for cell separation including mid2|
Components and Regulators of the S. pombe SIN
|cdc11p||Leucine rich repeat||Scaffold subunit; interacts with sid4p,spg1p, sid2p, cdc13p and cdc16p|
|ppc89p||SPB protein||Interacts with sid4p|
|sid4p||SPB protein||Interacts with cdc11p, plo1p and dma1p|
|spg1p||GTPase||Interacts with cdc11p and cdc7p; spg1p-GTP binds cdc7p which process downstream signaling|
|cdc16p||GAP||Regulates GTP hydrolysis of spg1p|
|byr4p||Scaffold protein||Regulates GTP hydrolysis of spg1p|
|cdc7p||Ser/Thr kinase||Binds to spg1p-GTP and process downstream signaling|
|sid1p||PAK-related kinase||Binds to cd14p and process SIN signaling downstream to cdc7p kinase|
|cdc14p||SIN component||Binds to sid1p and process SIN signaling downstream to cdc7p kinase|
|sid2p||AGC-kinase||Binds to mob1p and is recruited to medial region at the end of anaphase thus assumed to trigger ring contraction and septum formation|
|mob1p||MOB1/phocein family||Binds to mob1p and is recruited to medial region at the end of anaphase thus assumed to trigger ring contraction and septum formation|
|dma1p||FHA-RING finger protein||Prevents septation in spindle assembly checkpoint-arrested cells; may regulate plo1p localization at the SPB|
|zfs1p||Zinc-finger RNA binding protein||Prevents septation in spindle assembly checkpoint-arrested cells; targets unknown|
|scw1p||RNA binding protein||Rescues sid2p mutant alleles indirectly; probably through stabilization of microtubules|
|par1p||Regulatory subunit of PP2A||Negative regulator of SIN pathway; targets unknown|
|fin1p||NIMA-related kinase||Regulates spindle formation, affinity of plo1 for the SPB and activity of SIN at old pole.|
|rad24p||14-3-3 protein||Retains phosphorylated flp1p in cytoplasm|
|sce3p||A putative RNA-binding protein that is homologous to human eIF4B||Rescues mutations in cdc11p; targets unknown|
|dnt1p||Nucleolar protein||Interacts negatively with the SIN proteins; function unknown|
|flp1p/clp1p||Phosphoprotein phosphatase||Functions in cytokinesis checkpoint CDC14 homolog|
|etd1p||Possible GEF||Association of cdc7p and sid2p at the SPB; degradation could be linked to inactivation of SIN|
Keywords: cytokinesis, SIN, contractile ring, actin, myosin, Schizosaccharomyces pombe.
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