Document Detail


Disturbance of normal cell cycle progression enhances the establishment of transcriptional silencing in Saccharomyces cerevisiae.
MedLine Citation:
PMID:  7791768     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Previous studies have indicated that mutation of RAP1 (rap1s) or of the HMR-E silencer ARS consensus element leads to metastable repression of HMR. A number of extragenic suppressor mutations (sds, suppressors of defective silencing) that increase the fraction of repressed cells in rap1s hmr delta A strains have been identified. Here we report the cloning of three SDS genes. SDS11 is identical to SWI6, a transcriptional regulator of genes required for DNA replication and of cyclin genes. SDS12 is identical to RNR1, which encodes a subunit of ribonucleotide reductase. SDS15 is identical to CIN8, whose product is required for spindle formation. We propose that mutations in these genes improve the establishment of silencing by interfering with normal cell cycle progression. In support of this idea, we show that exposure to hydroxyurea, which increases the length of S phase, also restores silencing in rap1s hmr delta A strains. Mutations in different cyclin genes (CLN3, CLB5, and CLB2) and two cell cycle transcriptional regulators (SWI4 and MBP1) also suppress the silencing defect at HMR. The effect of these cell cycle regulators is not specific to the rap1s or hmr delta A mutation, since swi6, swi4, and clb5 mutations also suppress mutations in SIR1, another gene implicated in the establishment of silencing. Several mutations also improve the efficiency of telomeric silencing in wild-type strains, further demonstrating that disturbance of the cell cycle has a general effect on position effect repression in Saccharomyces cerevisiae. We suggest several possible models to explain this phenomenon.
Authors:
H Laman; D Balderes; D Shore
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  Molecular and cellular biology     Volume:  15     ISSN:  0270-7306     ISO Abbreviation:  Mol. Cell. Biol.     Publication Date:  1995 Jul 
Date Detail:
Created Date:  1995-07-27     Completed Date:  1995-07-27     Revised Date:  2009-11-19    
Medline Journal Info:
Nlm Unique ID:  8109087     Medline TA:  Mol Cell Biol     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  3608-17     Citation Subset:  IM    
Affiliation:
Department of Microbiology, College of Physicians & Surgeons of Columbia University, New York, New York 10032, USA.
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MeSH Terms
Descriptor/Qualifier:
Cell Cycle / genetics*
Cloning, Molecular
Cyclins / genetics
DNA-Binding Proteins
Fungal Proteins / genetics,  metabolism
Gene Dosage
Gene Expression Regulation, Fungal*
Genes, Fungal / genetics
Genes, Regulator
Hydroxyurea / pharmacology
Microtubule-Associated Proteins
Mutagenesis
Mutation
Peptide Biosynthesis
Peptides / genetics*
Regulatory Sequences, Nucleic Acid / genetics*
Ribonucleotide Reductases / genetics
Saccharomyces cerevisiae / genetics*
Saccharomyces cerevisiae Proteins*
Silent Information Regulator Proteins, Saccharomyces cerevisiae*
Telomere / genetics
Trans-Activators / genetics
Transcription Factors / genetics,  metabolism
Transcription, Genetic
Grant Support
ID/Acronym/Agency:
CA09503-0/CA/NCI NIH HHS; GM40094/GM/NIGMS NIH HHS
Chemical
Reg. No./Substance:
0/CIN8 protein, S cerevisiae; 0/Cyclins; 0/DNA-Binding Proteins; 0/Fungal Proteins; 0/MBP1 protein, S cerevisiae; 0/Microtubule-Associated Proteins; 0/Peptides; 0/SIR1 protein, S cerevisiae; 0/SIR4 protein, S cerevisiae; 0/SWI4 protein, S cerevisiae; 0/SWI6 protein, S cerevisiae; 0/Saccharomyces cerevisiae Proteins; 0/Silent Information Regulator Proteins, Saccharomyces cerevisiae; 0/Trans-Activators; 0/Transcription Factors; 127-07-1/Hydroxyurea; 61194-02-3/mating factor; EC 1.17.4.-/Ribonucleotide Reductases
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