Document Detail


Plc1p is required for proper chromatin structure and activity of the kinetochore in Saccharomyces cerevisiae by facilitating recruitment of the RSC complex.
MedLine Citation:
PMID:  19205744     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
High-fidelity chromosome segregation during mitosis requires kinetochores, protein complexes that assemble on centromeric DNA and mediate chromosome attachment to spindle microtubules. In budding yeast, phosphoinositide-specific phospholipase C (Plc1p encoded by PLC1 gene) is important for function of kinetochores. Deletion of PLC1 results in alterations in chromatin structure of centromeres, reduced binding of microtubules to minichromosomes, and a higher frequency of chromosome loss. The mechanism of Plc1p's involvement in kinetochore activity was not initially obvious; however, a testable hypothesis emerged with the discovery of the role of inositol polyphosphates (InsPs), produced by a Plc1p-dependent pathway, in the regulation of chromatin-remodeling complexes. In addition, the remodels structure of chromatin (RSC) chromatin-remodeling complex was found to associate with kinetochores and to affect centromeric chromatin structure. We report here that Plc1p and InsPs are required for recruitment of the RSC complex to kinetochores, which is important for establishing proper chromatin structure of centromeres and centromere proximal regions. Mutations in PLC1 and components of the RSC complex exhibit strong genetic interactions and display synthetic growth defect, altered nuclear morphology, and higher frequency of minichromosome loss. The results thus provide a mechanistic explanation for the previously elusive role of Plc1p and InsPs in kinetochore function.
Authors:
Parima Desai; Nilanjan Guha; Luciano Galdieri; Sara Hadi; Ales Vancura
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural     Date:  2009-02-11
Journal Detail:
Title:  Molecular genetics and genomics : MGG     Volume:  281     ISSN:  1617-4623     ISO Abbreviation:  Mol. Genet. Genomics     Publication Date:  2009 May 
Date Detail:
Created Date:  2009-04-24     Completed Date:  2009-05-28     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  101093320     Medline TA:  Mol Genet Genomics     Country:  Germany    
Other Details:
Languages:  eng     Pagination:  511-23     Citation Subset:  IM    
Affiliation:
Department of Biological Sciences, St John's University, 8000 Utopia Parkway, Queens, NY 11439, USA.
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MeSH Terms
Descriptor/Qualifier:
Base Sequence
Chromatin / genetics,  metabolism
Chromatin Assembly and Disassembly
DNA Primers / genetics
DNA, Fungal / genetics
DNA-Binding Proteins / genetics,  metabolism*
Genes, Fungal
Inositol Phosphates / metabolism
Kinetochores / metabolism
Mutation
Saccharomyces cerevisiae / genetics,  metabolism*
Saccharomyces cerevisiae Proteins / genetics,  metabolism*
Transcription Factors / genetics,  metabolism*
Type C Phospholipases / genetics,  metabolism*
Grant Support
ID/Acronym/Agency:
GM076075/GM/NIGMS NIH HHS
Chemical
Reg. No./Substance:
0/Chromatin; 0/DNA Primers; 0/DNA, Fungal; 0/DNA-Binding Proteins; 0/Inositol Phosphates; 0/RSC complex, S cerevisiae; 0/Saccharomyces cerevisiae Proteins; 0/Transcription Factors; EC 3.1.4.-/Type C Phospholipases; EC 3.1.4.3/Plc1 protein, S cerevisiae

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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