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The scutellum of germinated wheat grains undergoes programmed cell death: identification of an acidic nuclease involved in nucleus dismantling.
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PMID:  22888125     Owner:  NLM     Status:  Publisher    
Programmed cell death (PCD) is a crucial phenomenon in the life cycle of cereal grains. In germinating grains, the scutellum allows the transport of nutrients from the starchy endosperm to the growing embryo, and therefore it may be the last grain tissue to undergo PCD. Thus, the aim of this work was to analyse whether the scutellum of wheat grains undergoes PCD and to perform a morphological and biochemical analysis of this process. Scutellum cells of grains following germination showed a progressive increase of DNA fragmentation, and the TUNEL assay showed that PCD extended in an apical-to-basal gradient along the scutellum affecting epidermal and parenchymal cells. Electron-transmission microscopy revealed high cytoplasm vacuolation, altered mitochondria, and the presence of double-membrane structures, which might constitute symptoms of vacuolar cell death, whereas the nucleus appeared lobed and had an increased heterochromatin content as the most distinctive features. An acid- and Zn(2+)-dependent nucleolytic activity was identified in nuclear extracts of scutellum cells undergoing PCD. This nuclease was not detected in grains imbibed in the presence of abscisic acid, which inhibited germination. This nucleolytic activity promoted DNA fragmentation in vitro on nuclei isolated from healthy cells, thus suggesting a main role in nucleus dismantling during PCD.
Fernando Domínguez; Javier Moreno; Francisco Javier Cejudo
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Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2012-8-9
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Title:  Journal of experimental botany     Volume:  -     ISSN:  1460-2431     ISO Abbreviation:  J. Exp. Bot.     Publication Date:  2012 Aug 
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Created Date:  2012-8-13     Completed Date:  -     Revised Date:  -    
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Nlm Unique ID:  9882906     Medline TA:  J Exp Bot     Country:  -    
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Instituto de Bioquímica Vegetal y Fotosíntesis, Universidad de Sevilla and CSIC Avda Américo Vespucio, 49, 41092-Sevilla Spain.
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Journal ID (nlm-ta): J Exp Bot
Journal ID (iso-abbrev): J. Exp. Bot
Journal ID (hwp): jexbot
Journal ID (publisher-id): exbotj
ISSN: 0022-0957
ISSN: 1460-2431
Publisher: Oxford University Press, UK
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© 2012 The Authors.
Print publication date: Month: 9 Year: 2012
Electronic publication date: Day: 9 Month: 8 Year: 2012
pmc-release publication date: Day: 9 Month: 8 Year: 2012
Volume: 63 Issue: 15
First Page: 5475 Last Page: 5485
ID: 3444264
PubMed Id: 22888125
DOI: 10.1093/jxb/ers199

The scutellum of germinated wheat grains undergoes programmed cell death: identification of an acidic nuclease involved in nucleus dismantling
Fernando Domínguez1
Javier Moreno2
Francisco Javier Cejudo1*
1Instituto de Bioquímica Vegetal y Fotosíntesis, Universidad de Sevilla and CSICAvda Américo Vespucio, 49, 41092-SevillaSpain
2Departamento de Biología Celular, Facultad de Biología, Universidad de SevillaAvda Reina Mercedes s/n, 41012 -SevillaSpain
Correspondence: * To whom correspondence should be addressed. E-mail:


The programmed elimination of unwanted cells is an essential process of development of animals and plants. The two most common forms of cell death in animals are apoptosis and autophagy, which can be distinguished by morphological and molecular features (Conradt, 2009). Apoptosis is characterized by a series of well-defined morphological changes including cell shrinkage, cytoplasm contraction, and chromatin condensation prior to the final engulfment by phagocytic cells (Taatjes et al., 2008). At the molecular level, apoptosis is characterized by activation of caspases (cysteinyl, aspartate-specific proteases) and nuclear DNA fragmentation (Kitazumi and Tsukahara, 2011). In contrast, autophagy is characterized at the morphological level by the presence of autophagic vesicles (autophagosomes) within the dying cells and the absence of engulfment by phagocytes during early stages of the cell-death process (He and Klionsky, 2009). Despite these differences between the two mechanisms of cell death, genetic studies carried out in different animal models have identified genes involved both in autophagy and apoptosis (Conradt, 2009). Besides caspases, there are a variety of apoptogenic effectors supporting the cellular suicide programme that leads to internucleosomal DNA fragmentation and nuclear condensation, such as caspase-activated DNase (CAD), mitochondrial endonuclease G (EndoG), DNaseI, DNaseII, apoptosis-inducing factor (AIF) (for review, see Samejima and Earnshaw, 2005), and apoptosis chromatin condensation inducer in the nucleus (Acinus) (Sahara et al., 1999).

In plants, programmed cell death (PCD) is both an important process of development (Kuriyama and Fukuda, 2002) and a mechanism of defence against pathogens (Lam, 2004). Whilst plant PCD shares some similarities with apoptosis of animals, such as internucleosomal fragmentation of DNA, chromatin condensation, and activation of caspase-like proteases (Bai et al., 2010), PCD in plant cells also exhibit distinctive features. The presence of chloroplasts, a prominent vacuole, and the cell wall are unique characteristics of plant cells, which affect PCD (Williams and Dickman, 2008). In the case of the chloroplasts, which constitute an important source of reactive oxygen species production in plant cells, it was proposed that these organelles may have a signalling function of some plant PCD responses (Zapata et al., 2005). Moreover, a combination of the function of the vacuole during cell death and autophagy may represent a plant alternative to the phagocytosis system of apoptosis (Hatsugai et al., 2006; Bassham, 2007), which has a specific morphology termed ‘vacuolar cell death’ (van Doorn et al., 2011). At the molecular level, although there is increasing evidence which connects the participation of proteases and nucleases in plant PCD, the enzymes directly involved in the execution of nucleus dismantling in plants (chromatin condensation, internucleosomal fragmentation of DNA, and nuclear envelope disorganization) are yet poorly known.

PCD plays an essential role in the processes of development and germination of cereal grains and, thus, the cereal grain has become one of the model systems for the study of PCD in plants. At initial stages of grain development, maternal tissues such as the nucellus and the nucellar projection cells degenerate by a process of PCD associated with characteristic proteolytic and nucleolytic activities (Domínguez and Cejudo, 1998, 2006; Domínguez et al., 2001). Then the starchy endosperm, the tissue specialized in the accumulation of storage compounds, undergoes PCD during maturation (Young et al., 1997; Young and Gallie, 1999, 2000). Germination and postgermination of cereal grains occurs by an ordered sequence of events, which are subjected to hormonal regulation and may be summarized as follows: gibberellins are synthesized at the scutellum and diffuse to the starchy endosperm (Appleford and Lenton, 1997). The hormone is perceived by the aleurone cells, which induce the synthesis and secretion of hydrolytic enzymes, including α-amylases, proteases, and glucanases, and also the acidification of the starchy endosperm, a process that occurs with a well-established spatiotemporal pattern, as described for the wheat grain (Domínguez and Cejudo, 1999). Once the aleurone cells have carried out their essential role, these cells initiate a process of PCD, which is also under the control of gibberellins (Fath et al., 2000; Domínguez et al., 2004). Besides its initial role to produce gibberellins, the major function of the scutellum in the germinated grain is the transfer of sugars and amino acids to the growing seedling (West et al., 1998; Aoki et al., 2006). In addition, the scutellum is itself a storage tissue, the contents of which might be used to feed the seedling once the transfer function is finished. So far, the analysis of PCD in the scutellum has been limited to studies of embryogenesis during maize kernel development (Giuliani et al., 2002; Consonni et al., 2003) or differentiating vascular tissue of germinated grains (Domínguez et al., 2002). However, it is not yet known whether the scutellum undergoes a massive process of PCD during grain germination. The present study addressed whether scutellar cells suffer PCD in germinated wheat grains and the identification of nucleolytic activities involved in nucleus dismantling. The aim was to compare the morphological and biochemical features of this death process with those of other tissues undergoing PCD in cereal grains, such as starchy endosperm, aleurone, or nucellar cells. The relevance of this process of PCD of the scutellum in the context of grain germination is discussed.

Materials and methods
Plant material

Wheat (Triticum aestivum cv. Chinese Spring) grains were sterilized in 2% (v/v) NaOCl for 20min and washed twice with sterile water, once with 0.01M HCl and then thoroughly with sterile distilled water. Sterile grains were allowed to germinate at room temperature on sterile filter paper soaked with water. Treatments with hormones and inhibitors of hormone synthesis were carried out on filter paper soaked with 20mM MOPS-KOH pH 7.0 supplemented with 10mM CaCl2. Hormones and inhibitors were added at the following final concentrations: gibberellic acid, GA3, 5 µM; abscisic acid (ABA), 25 µM; paclobutrazol (PCB), 500 µM; 24-epibrassinolide (EBL), 1nM, and α-(2-aminoethoxyvinyl) glycine (AVG), 10 µM. GA3, ABA, EBL, and AVG were purchased from Sigma Chemical and PCB from Duchefa Biochimie.

Isolation of DNA and electrophoresis

Scutellum discs, dissected from wheat grains imbibed for up to 7 days, were ground in liquid nitrogen with a mortar and pestle to a fine powder and homogenized in 5ml of extraction buffer [50mM TRIS-HCl pH 8.0, 100mM NaCl, 50mM EDTA, 1% (v/v) 2-mercaptoethanol, and 2% (w/v) SDS]. For DNA isolation, extracts were incubated at 45 °C for 15min, at room temperature for 30min, and then mixed with 5ml of phenol/chloroform (1:1, v/v). Samples were centrifuged at 10,000 g for 10min and the upper phase was precipitated at –20 °C for 30min with 2 volumes of ice-cold ethanol. After centrifugation, the DNA pellet was air dried, dissolved in 250 µl TE buffer (10mM TRIS-HCl pH 8.0, 1mM EDTA), and quantified spectrophotometrically. RNase A (1.5 µl of a stock of 10mg ml–1) was added and incubated at 37 °C for 3h. After this treatment, DNA was again precipitated and dissolved in TE buffer. Finally, DNA samples (20 µg) were analysed on a 2% agarose gel and stained with ethidium bromide. DNA ladders (500 or 100bp, Gibco) were used to estimate DNA size.

Preparation of nuclear and cytoplasmic extracts

Scutellum discs dissected from grains imbibed for up to 7 days were ground in a mortar with liquid nitrogen and resuspended in 5ml homogenization buffer [0.25M sucrose, 10mM NaCl, 10mM MES-NaOH pH 6.0, 5mM EDTA, 0.15mM spermine, 0.5mM spermidine, 0.2mM PMSF, 20mM 2-mercaptoethanol, 0.25 % (v/v) Triton X-100]. The homogenate was clarified by centrifugation at 100 g for 1min and filtered through a nylon mesh (60 µm pore-size, Millipore). Fractionation was performed by adding the filtered supernatant to homogenization buffer containing 30% Percoll and centrifugation at 3000 g for 15min. The upper phase was collected as the cytoplasmic extract, the Percoll phase was discarded, and the nuclei-enriched pellet was washed in homogenization buffer and resuspended in 100 µl extraction buffer [25mM sodium phosphate pH 7.8, 40mM KCl, 20% glycerol, 1% plant protease inhibitor cocktail (Sigma), 0.4M (NH4)2SO4]. After extraction on ice for 30min, the supernatant of the subsequent centrifugation (13,000 g, 20min, 4 °C) was collected as the nuclear extract.

TUNEL assay

Wheat grains harvested at different days after imbibition (DAI) were longitudinally sectioned after removing shoots and roots, immediately fixed in FAE (formaldehyde/acetic acid/ethanol (3.7:5:50, v/v, and embedded in Paraplast Plus (Sigma). In situ detection of DNA fragmentation was carried out as previously described (Domínguez et al., 2001). Paraplast Plus was removed from the grain sections by treatment with xylol, and the sections were then dehydrated with a decreasing ethanol series, treated with proteinase K (20 µg ml–1) in PBS (10mM sodium phosphate buffer, 130mM NaCl), and rinsed twice with PBS. Endogenous peroxidase activity was then quenched by incubation in 1% (v/v) H2O2 in methanol for 30min and rinsed twice with PBS. For labelling, sections were incubated for 60min at 37 °C in the presence of terminal deoxynucleotidyl transferase (TdT) with the In situ Cell Death Detection Kit (Roche Applied Systems), according to the manufacturer’s instructions. Controls were performed in which TdT was omitted.

Electron microscopy

For morphological analysis, small fragments of wheat grains harvested at 1 or 5 DAI were fixed in 4% (v/v) glutaraldehyde prepared in 0.1M cacodylate buffer (pH 7.2) for 3h at 4 °C. The samples were dehydrated in an acetone series and embedded in Epon (an epoxy embedding medium). Toluidine blue-stained semi-thin sections used as control were viewed in a Leitz (Aristoplan) light microscope. Thin sections (60–80nm) were cut on a Reichert-Jung Ultracut E ultramicrotome, stained with uranyl acetate and lead citrate, and examined in a Philips CM-10 transmission electron microscope.

In-gel nuclease activity assay

The in-gel nuclease activity assay was performed as reported previously (Domínguez et al., 2004) with modifications. Cytoplasmic and nuclear extracts (50 µg protein) obtained as described above were fractionated on SDS-PAGE gels containing 0.3mg ml–1 salmon sperm DNA at 4 °C and 20 mA/plate. After electrophoresis, the gels were washed twice for 15min in 1% (v/v) Triton X-100 and then twice for 15min in distilled water. The gels were then incubated overnight in 25mM sodium acetate-acetic acid buffer (pH 5.5, containing 1mM ZnSO4 and 0.2mM DTT) or 100mM MOPS-KOH (pH 7.0, containing 5mM CaCl2 and 5mM MgCl2) at 37 °C. False nucleolytic activities associated with DNA-binding proteins were discarded by incubating the gels in 1% (w/v) SDS for 2h at room temperature and then washed in water for 10min. Finally, gels were stained with 1 µg ml–1 ethidium bromide for 10min. Nuclease activities were photographed on a UV light box. Cytoplasmic contamination of plant nuclear extracts was routinely analysed by Western blot analysis using phosphoenolpyruvate carboxylase (PEPC) as a cytoplasmic marker (González et al., 1998). Affinity-purified polyclonal maize PEPC antibodies were purchased from Rockland.

In vitro endonuclease activity assay

In vitro endonuclease activity assay was carried out according to the method described by Ito and Fukuda (2002) with modifications. In brief, isolated nuclei from scutellar tissue were incubated with nuclear or cytoplasmic extracts from scutellum isolated from grains at 7 DAI. Incubation was performed for 2h at 30 °C in 25mM sodium acetate-acetic acid buffer (pH 5.5) or 100mM MOPS-KOH (pH 7.0). Reactions were stopped by adding an equal volume of lysis buffer (100mM TRIS-HCl pH 8.0, 200mM NaCl, 100mM EDTA, 2% SDS) and incubation for 1h at 55 °C. After extraction with phenol/chloroform/isoamylalcohol (25:24:1, v/v), DNA was precipitated with two volumes of absolute ethanol, resuspended in TE buffer, precipitated again, and finally resuspended in 25 µl TE buffer. Contaminating RNA was removed by incubation for 3h at 37 °C in the presence of RNaseA (final concentration 60 µg ml–1). DNA was then ethanol-precipitated, resuspended in TE buffer, resolved on 2% (w/v) agarose gels, and visualized using ethidium bromide.

The scutellum of wheat grains following germination undergoes PCD

With the aim of testing whether the scutellum of germinated wheat grains undergoes PCD, this study analysed the internucleosomal fragmentation of genomic DNA, a hallmark of PCD. DNA laddering was first observed in grains after 4 DAI and increased progressively up to 7 days (Fig. 1A). A more precise identification of scutellar cells undergoing PCD was performed with the TdT (terminal deoxynucleotidyl transferase)-mediated dUDP nick-end labelling (TUNEL) assay. No labelling was observed in sections of grains at 1 DAI (Fig. 1B) thus revealing the absence of PCD in scutellar cells at these early stages; however, the TUNEL assay showed labelling of nuclei of the parenchymal and epidermal cells of grains at 7 DAI (Fig. 1C). In the central region of the scutellum, TUNEL staining of the epithelial and parenchymal cells was first observed in grains after 4 DAI and increased progressively up to 7 DAI (Fig. 1D–H), in agreement with the detection of DNA laddering (Fig. 1A). No labelling over background was observed in control sections in the absence of TdT (Fig. 1I).

Previous analysis of postgerminative processes in wheat grains revealed important spatiotemporal gradients affecting starchy endosperm acidification, aleurone gene expression, and PCD (Domínguez and Cejudo, 1999; Domínguez et al., 2004). Thus, with the aim of testing whether scutellum PCD takes place with any spatiotemporal pattern, ultrathin sections of wheat grains at 1 and 5 DAI were analysed. A morphological symptom of cell death, the increase of vacuolization, progressed from the upper part of the scutellar epithelium in contact with the aleurone layer to the lower part, which is indicative of a gradient of PCD in this scutellar tissue (Fig. 2A, 2B). It was noticed that PCD was initiated in scutellar cells once the aleurone cells close to the scutellum had completed the process of PCD and were almost empty (Fig. 2B). The TUNEL assay confirmed this pattern of PCD since in wheat grains at 7 DAI most cells of the upper part of the scutellum showed an intense labelling, whereas staining of cells of the lower part was less intense (Fig. 2C). These results suggest that the spatial progression of PCD in the scutellum occurs with an apical-to-basal gradient.

Morphology of scutellum cells undergoing PCD

To study the morphological features of scutellum PCD, this study focused on the analysis of epithelium and parenchyma cells of grains at 5 DAI, considering separately cytoplasmic and nuclear events. Characteristic features of the cytoplasm of cells undergoing death, as observed in the epithelium, are the formation of provacuoles originated from Golgi cisternae or endoplasmic reticulum-derived bodies (Fig. 3A, 3B), which appear in great number and probably assume the role of hydrolytic enzymes storage, until these provacuoles fuse with the central vacuole (Fig. 3C). This death process was also characterized by double-membrane vesicles sequestering portions of cytoplasm (Fig. 3D, 3E), which resembled autophagosomes of animal cells undergoing autophagy. Moreover, several alterations of mitochondria could be observed including irregular shape, enlargement, and broken cristae (Fig. 3D–F). In the cytoplasm, another autolytic compartment characterized by an electron-translucent cytoplasm could be distinguished: storage vacuoles evolving to lytic vacuoles (Fig. 3E). In addition, characteristic membranous structures could be observed in dying scutellum cells such as multilamellar structures (Fig. 3G) or the whorls formed from cytoplasmic membranes (Fig. 3H).

Concerning the nucleus, the characteristics observed in parenchymal scutellum dying cells include high heterochromatin content and deep invaginations (Fig. 4A), so that narrow layers of cytoplasm are confined between nuclear segments (Fig. 4B; white arrows). A clear symptom of nuclear degradation is the presence of remnants of heterochromatin inside provacuoles (Fig. 4C, white arrowheads), leaking to the central autolytic vacuole (Fig. 4C, black arrowheads). Overall, the morphological features identified suggest that scutellum epithelial and parenchymal cells of wheat grains following germination undergo vacuolar cell death, as described in other plant tissues (van Doorn et al., 2011).

A nuclear-localized acid endonucleolytic activity in scutellum cells undergoing PCD

As shown above, DNA fragmentation was identified as a hallmark of scutellum PCD. To characterize this process at the biochemical level, the nucleases localized in the nucleus of cells undergoing PCD were analysed by in-gel activity assays. For that purpose, scutellum cells were fractionated into nuclear and cytoplasmic fractions according to the scheme depicted in Supplementary Fig. S1A (available in JXB online). Nuclei isolated from scutellar cells at early stages (1–4 DAI) appeared intact, whereas at 7 DAI showed a lobed and fragmented appearance (Supplementary Fig. S1B). Protein extracts from both cytosolic and nuclear fractions were subjected to analysis of nucleolytic activity. A band showing endonuclease activity, with a molecular mass of approximately 70kDa, was detected in nuclear extracts from scutellum cells of wheat grains at 7 DAI when assayed at acid pH, but not at neutral pH (Fig. 5A, 5B). In contrast, cytoplasmic fractions showed no detectable nucleolytic activity when assayed at acidic pH, but showed different neutral nucleases (Fig. 5A, 5B). Possible contamination of nuclear fractions with cytoplasmic proteins was ruled out by routinely testing for PEPC, a cytoplasmic enzyme, in the Western blot analysis (Fig. 5C).

To further characterize the process of DNA fragmentation, cell-free assays were carried out by incubating either the nuclear or cytoplasmic extracts from scutellum cells undergoing PCD (at 7 DAI) with intact nuclei isolated from healthy scutellum cells (at 1 DAI). The nucleolytic activity of the nuclear extracts triggered the internucleosomal fragmentation of DNA in intact nuclei at acid pH in contrast to the cytoplasmic extracts, which did not produce any DNA fragmentation or increase the activity of the nuclear extract (Fig. 5D). In agreement with the in-gel activity results, the nuclear-localized nucleolytic activity is acidic, as shown by the low activity detected at neutral pH (Fig. 5E). In addition, the requirement of cations of this nuclear-localized nucleolytic activity was analysed using both in-gel and in vitro assays. Fig. 6A shows the activating effect of Zn2+ on the nuclease, whereas Ca2+ and Mg2+ had no effect. In vitro assays confirmed the activating effect of Zn2+ (Fig. 6B). The cation requirement of the nuclear-localized nucleolytic activity was in contrast with the cytoplasmic activities, which required Ca2+ and/or Mg2+ and were strongly inhibited by Zn2+ (Supplementary Fig. S2A). Although the nucleolytic activities of the cytoplasmic extracts did not produce DNA fragmentation in intact nuclei, as shown in the cell-free assay (Fig. 5D, 5E), these activities effectively degraded naked DNA, producing an unspecific DNA smear (Supplementary Fig. S2B). Therefore, the nucleolytic activity of nuclear extracts is associated with PCD and is able to produce DNA fragmentation on an intact chromatin structure, being Zn2+- and acid pH-dependent.

ABA inhibits germination and DNA fragmentation of scutellum cells

The finding of a spatiotemporal pattern of PCD in the scutellum (Fig. 2C), and the fact that PCD starts once the proximal aleurone cells have undergone PCD, suggested that scutellum PCD is tightly regulated. As hormones play an important role in the control of grain germination and early seedling growth, the effect of hormones and inhibitors of hormone synthesis on scutellum PCD was analysed. For that purpose, wheat grains were imbibed in the presence of different hormones (GA3, ABA, or the brassinosteroid EBL) and PCB, an inhibitor of GA synthesis, or AVG, an inhibitor of ethylene synthesis. As expected, ABA, and to lower extent PCB, exerted an inhibitor effect on wheat grain germination and seedling growth, whereas GA3 and AVG did not significantly affect the postgerminative process and EBL treatment reduced root elongation (Supplementary Fig. S3). The analysis of DNA fragmentation of scutellum cells showed that only ABA treatment exerted a clear inhibitory effect (Fig. 7A). The other treatments, including PCB or EBL, which affected the postgerminative process, did not show any significant effect (Fig. 7A). In agreement with these results, the in-gel nuclease assay identified the acid nucleolytic activity in nuclear extracts from scutellum cells, with the exception of the ABA-treated grains (Fig. 7B). Similarly, ABA caused a significant inhibition of the nuclear-localized nucleolytic activity, as detected by in vitro assays (Fig. 7C). Thus, only ABA treatment, which had a strong effect on germination, was effective to inhibit the biochemical symptoms of PCD of the scutellar cells.


The success of cereal grain germination and initial stages of seedling growth depends on the precise organization of events taking place during this process. Because the aleurone cells are able to perceive gibberellins and induce the synthesis and secretion of hydrolytic enzymes, these cells play a central role to mobilize the storage material of the starchy endosperm and have received more attention than any other grain tissue. Interestingly, once the aleurone cells have performed their important function, enter in a process of PCD, which is also activated by gibberellins (Bethke et al., 1999), thus allowing the use of the aleurone cellular contents for seedling growth. Although the scutellum has received less attention, it is clearly a tissue essential for germination. Indeed, gibberellins, the hormones activating germination, are synthesized in the scutellum (Appleford and Lenton, 1997). Moreover, scutellum epithelium cells participate at very initial steps of starchy endosperm mobilization by the secretion of hydrolytic enzymes together with the aleurone layer (Okamoto et al., 1980; Cejudo et al., 1995; Domínguez and Cejudo, 1995). Nevertheless, the major function of the scutellum of germinated grains is to serve as transfer route for peptides (West et al., 1998) and sugars (Aoki et al., 2006) for the growing seedling. The present study addressed whether the scutellum of wheat grains undergoes PCD following germination, so that their cellular contents are also used by the growing seedling, and how scutellum and aleurone cell death is coordinated into the overall organization of germination and postgermination. In addition, this study characterized scutellum cell death morphologically and biochemically.

Analysis of genomic DNA from scutellum discs of grains at different days after imbibition showed a progressive appearance of DNA laddering (Fig. 1A), which is indicative of PCD. The occurrence of PCD was further confirmed with the TUNEL assay, which revealed that both epithelial and parenchymal cells of the scutellum undergo PCD, based on the intense labelling of nuclei of these tissues. Scutellum PCD took place with a characteristic spatiotemporal pattern, so that it was initiated at the apical region and progressed towards the basal side of the scutellum (Fig. 2C). A remarkable feature of scutellum PCD is that it proceeds when proximal aleurone cells showed symptoms to have completed the death process. Based on these results, it may be concluded that scutellum PCD is coordinated with aleurone PCD. Moreover, the progressive advance and the spatiotemporal pattern of scutellum PCD may indicate that the function of this tissue, to transfer nutrients from the starchy endosperm to support initial seedling growth, does not cease abruptly once the process of PCD is initiated.

The spatial pattern of scutellar PCD suggests the existence of a signal to control the process. It is known that scutellum cells suffer oxidative stress in germinating grains (Serrato and Cejudo, 2003; Bailly, 2004) and that these cells possess different detoxifying systems such as catalase and superoxide dismutase (Mylona et al., 2007) and 1-Cys peroxiredoxin, a peroxidase specifically and highly expressed in seeds and localized in nuclei of scutellum and aleurone cells (Stacy et al., 1999; Pulido et al., 2009). Indeed, reactive oxygen species production has an active role in aleurone cell death (Fath et al., 2001; Beligni et al., 2002; Wu et al., 2011). Since aleurone cells proximal to the top region of the scutellum have undergone PCD, a possible explanation of the apical-to-basal pattern of scutellum PCD is that it is due to a signal originated at the apical-proximal side aleurone cells, but much work is still needed to test this possibility.

Once established the occurrence of PCD in the scutellum of germinated wheat grains, the morphological features of this process were analysed. Scutellar cells undergoing PCD show vacuolization in the cytoplasm and a proactive intramembrane system (Figs. 2B and 3) linking the intracellular secretory pathway to a process of vacuolar cell death (van Doorn et al., 2011). The presence of precursor protease vesicles and autolytic compartments derived from the endoplasmic reticulum (Toyooka et al., 2000; Greenwood et al., 2005) and Golgi cisternae (Filonova et al., 2000) are considered as features of plant cell death, resembling morphological features of autophagy in animal cells. Although the role of autophagy in cell death is still subject of discussion (Kroemer and Levine, 2008), both morphological and biochemical evidence suggests that autophagy has a pro-death function either in developmental (Bozhkov et al., 2005a) or pathogen-induced PCD in plants (Liu et al., 2005; Hofius et al., 2009). A feature of scutellum PCD is the appearance of different degrees of structural alterations of mitochondria (Fig. 3F). In other eukaryotic cells, mitochondria membranes have been described as origin of autophagosomes (Hernández et al., 2003; Ning et al., 2006; Luo et al., 2009; Hailey et al., 2010). This role of mitochondria in autophagy-type PCD is different from the role that these organelles have in apoptosis-type PCD, in which the disruption of the mitochondria promotes the translocation of cytochrome c and other apoptogenic factors to the cytoplasm (Lam, 2004).

Concerning the nucleus, it adopts a characteristic lobed morphology and a higher heterochromatin content (Fig. 4) as the most relevant features. However, remnants of heterochromatin could be detected in the central autolytic vacuoles (Fig. 4C), as observed in dying cells of somatic embryos of Norway spruce (Filonova et al., 2000), which suggests that the nucleus is dismantled as cell death progresses. The identification of biochemical components participating in nucleus dismantling was another objective addressed in this study.

At the molecular level, the knowledge of enzymes involved in the execution of PCD in plants is much lower than in animals. Despite the absence of genes encoding caspases in plants, it appears that caspase-like activities are important (del Pozo and Lam, 1998). Of the different proteases proposed to participate in plant PCD, only some of them seem to be essential components for nucleus dismantling. This is the case of metacaspase mcII-Pa, which is translocated to the nucleus in cells undergoing PCD during embryogenesis (Bozhkov et al., 2005b) and participates in cleavage and activation of TSN, a phylogenetically conserved multifunctional regulator of gene expression involved in PCD (Sundström et al., 2009). The present study used the wheat grain as a model system to identify nuclear-localized factors involved in the final steps of PCD execution, critically on DNA fragmentation and nucleus dismantling. Biochemical analysis allowed the identification of two Ca2+/Mg2+ endonucleases, which were localized, respectively, to the nuclei of aleurone cells (Domínguez et al., 2004) and nucellus cells (Domínguez and Cejudo, 2006) undergoing PCD. Although both endonucleases showed the same cation requirements, the different electrophoretic mobility suggested that each tissue of wheat grains undergoes PCD with the participation of different nucleases. The identification of a Zn2+-dependent endonuclease in the nucleus of wheat scutellum cells undergoing PCD, which produced internucleosomal fragmentation of DNA (Figs. 5–7), is in agreement with the proposal of the participation of different nucleases in different grain tissues. Among the endonucleases identified in cells suffering PCD, only some have been directly involved in nuclear dismantling. This is the case of ZEN1, a Zn2+-dependent nuclease implicated in the degradation of nuclear DNA in Zinnia tracheary elements (Ito and Fukuda, 2002). ZEN1 is localized to vacuoles which collapse before DNA is degraded (Obara et al., 2001). However, ZEN1 activity did not produce the characteristic DNA laddering shown in animal apoptosis. In plants, it was proposed that nucleus-localized nucleases are neutral whereas vacuolar nucleases are acidic (Sugiyama et al., 2000). Thus, the identification of an acidic Zn2+-dependent endonuclease in the nucleus of wheat scutellum cells undergoing PCD may be considered an exception to this rule, to be added to the previously reported acidic Zn2+-dependent nuclease responsible for DNA laddering identified in rice root tip cells undergoing PCD in response to salt stress (Jiang et al., 2008).

The appearance of the nuclear-localized nucleolytic activity was completely inhibited in ABA-treated grains (Fig. 7), which might suggest an inhibitory effect of ABA on nuclease expression. However, it is well known that the success of germination depends of a spatiotemporal sequence of events. Most probably, the strong inhibitory effect of ABA on germination (Supplementary Fig. S3) occurs because it counteracts the activating effect of gibberellins, thus arresting germination at early stages. As a consequence, the rest of events taking place thereafter, including scutellum PCD, will not take place in ABA-treated grains.

Supplementary Material Supplementary Data
Supplementary Data

Supplementary material

Supplementary data are available at JXB online.

Supplementary Fig. S1. Cytoplasm and nuclei fractionation and visualization of isolated nuclei

Supplementary Fig. S2. Characterization of nucleolytic activities in the cytoplasm of scutellum cells undergoing PCD

Supplementary Fig. S3. Effect of hormones on root and shoot emergence and elongation


This work was funded by the European Regional Development Fund (ERDF) through the Ministerio de Ciencia e Innovación (grant no. BIO2010-15430) and Junta de Andalucía (grant nos. CVI-5919 and BIO-182).

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[Figure ID: F1]
Fig. 1.  

Pattern of DNA fragmentation in scutellum cells of wheat grains following germination. (A) Wheat grains were imbibed and at the days indicated scutella were dissected and immediately frozen in liquid nitrogen. DNA (20 µg) isolated from each sample was fractionated on 2% (w/v) agarose gels. The size of the DNA molecular markers are indicated on the right. (B–I) Longitudinal sections of wheat grains after 1 (B, D), 3 (E), 5 (F), 6 (G), or 7 (C, H, I) days after imbibition were subjected to the TUNEL assay. Control sections (I) were incubated in the absence of TdT enzyme. Analyses were repeated at least three times on independent biological samples and representative results are shown. al, Aleurone layer; en, starchy endosperm; se, scutellar epithelium; sp, scutellar parenchema. Bars, 100 µm (B, C) and 50 µm (D–I).

[Figure ID: F2]
Fig. 2.  

Apical-to-basal gradient of programmed cell death in the scutellum of wheat grains following germination. (A, B) Light microscopy of toluidine blue-stained ultrathin sections of wheat grains 1 (A) and 5 (B) days after imbibition. Note the nuclei enlargement and the increasing vacuolation in the epithelium of the scutellum. (C) TUNEL assay of nuclear DNA fragmentation in longitudinal sections of wheat grains 7 days after imbibition. The TUNEL assay was performed at least three times and a representative scutellum section is shown. al, Aleurone layer; en, starchy endosperm; se, scutellar epithelium; sp, scutellar parenchema. Bars, 50 µm (A, B) and 100 µm (C) (this figure is available in colour at JXB online).

[Figure ID: F3]
Fig. 3.  

Morphological analysis of cytoplasm of epithelial scutellum cells in germinated wheat grains at 5 days after imbibition. (A, B) Scutellar epithelium cell showing a vacuolated cytoplasm in the proximity of the heterochromatinized nucleus: nu, nucleus; mt, mitochondria; pv, provacuole. (C) A central autolytic vacuole (cv) is formed. (D–G) Appearance of disturbed mitochondria (dmt) and double-membrane vesicles (dmv) at the onset of programmed cell death: in G, note the multilamellar body (mlb) sequestering part of the cytoplasm; psv, protein storage vacuole. (H) Characteristic membrane structures localized in dying cells: wh, whorl formed by the cytoplasmic membrane. Bars, 1 µm (A, B, C, D, H), 2 µm (E), and 0.5 µm (F, G).

[Figure ID: F4]
Fig. 4.  

Morphological analysis of nuclei of parenchymal scutellum cells in germinated wheat grains at 5 days after imbibition. (A, B) Detail of a nucleus with invaginations (white arrows) and protein storage vacuoles in its proximity. (C) Remnants of condensed chromatin inside provacuoles (white arrowheads) or central vacuole (black arrowheads). cv, central vacuole; nu, nucleus; psv, protein storage vacuoles; pv, provacuole. Bars, 0.5 µm (A), 5 µm (B), and 1 µm (C).

[Figure ID: F5]
Fig. 5.  

Identification of an acid nuclease in the nucleus of scutellum cells undergoing programmed cell death. (A–C) Scutellum discs dissected from wheat grains at 1, 4, or 7 days after imbibition (DAI), as indicated, were fractionated into cytoplasmic and nuclear extracts, and aliquots from both fractions (25 µg protein) were analysed by in-gel nuclease assay at the indicated pH. C, Fractions (15 µg protein) were subjected to Western blot analysis and probed with polyclonal anti-PEPC antibodies. Molecular-mass marker, in kDa, is indicated on the left. (D, E) In vitro analysis of nuclear DNA fragmentation. Protein extracts (4 µg protein) from nuclear (N), cytoplasmic (C), or a mixture of both (N+C) fractions obtained from scutellar cells of grains at 7 DAI were incubated with intact nuclei isolated from wheat grains at 1 DAI at the indicated pH. Following incubation, nuclear DNA was isolated and aliquots (20 µg) were fractionated on 2% (w/v) agarose gels. DNA marker, in kbp, is indicated on the left. Assays were repeated at least three times with similar results and representative results are shown.

[Figure ID: F6]
Fig. 6.  

Characterization of nucleolytic activities in the nucleus of scutellum cells undergoing programmed cell death. (A) Effect of cations on nucleolytic activities. Protein extracts (25 µg protein) from nuclear fractions were subjected to in-gel nuclease assay by overnight incubation at 37 °C in 25mM sodium acetate-acetic acid buffer (pH 5.5) containing 0.2mM DTT and supplemented as indicated with 1mM CaCl2, 1mM MgCl2, or 1mM ZnSO4. EDTA was added to a final concentration of 0.1mM. Molecular-mass markers, in kDa, are indicated on the left. (B) In vitro analysis of nuclear DNA fragmentation. Protein extracts (4 µg protein) from nuclear fractions from scutellar cells of wheat grains at 7 days after imbibition (DAI) were incubated with intact nuclei isolated from scutellum cells of grains at 1 DAI. Incubations were performed for 2h at 30 °C in 25mM sodium acetate-acetic acid buffer (pH 5.5) containing 0.2mM DTT. ZnSO4 and EDTA were added to the indicated concentration. DNA was fractionated on 2% (w/v) agarose gels. DNA markers, in kbp, are indicated on the left. Assays were repeated at least three times with similar results and representative results are shown.

[Figure ID: F7]
Fig. 7.  

Effect of hormones on scutellum programmed cell death. Wheat grains were soaked for 7 days in the absence or presence of the following hormones or hormone synthesis inhibitors: 5 µM GA3, 500 µM PCB, 25 µM ABA, 1nM EBL, or 10 µM AVG (final concentrations). (A) After imbibition, scutellum discs were dissected and genomic DNA was isolated and analysed in 2% (w/v) agarose gel. DNA markers, in kbp, are indicated on the left. (B) Nuclear extracts (25 µg protein) were analysed by in-gel nuclease assay by overnight incubation at 37 °C in 25mM sodium acetate-acetic acid buffer (pH 5.5) containing 1mM ZnSO4 and 0.2mM DTT. Molecular-mass markers, in kDa, are indicated on the left. (C) In vitro analysis of nuclear DNA fragmentation. Protein extracts (4 µg protein) from nuclear fractions from scutellar cells of wheat grains under different hormonal treatment (7 days after imbibition, DAI) were incubated with intact nuclei isolated from scutellum discs of grains at 1 DAI. Incubations were performed for 2h at 30 °C in 25mM sodium acetate-acetic acid buffer (pH 5.5) containing 1mM ZnSO4 and 0.2mM DTT. DNA was fractionated on 2% (w/v) agarose gels. DNA markers, in kbp, are indicated on the left. Assays were repeated at least three times with similar results and representative results are shown. AB, ABA; AV, AVG; E, EBL; G, GA3; P, PCB.

Article Categories:
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Keywords: Key words: cell death, germination, nuclease, scutellum, seed, Triticum aestivum (wheat).

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