Title | Dominant mutants of the Saccharomyces cerevisiae ASF1 histone chaperone bypass the need for CAF-1 in transcriptional silencing by altering histone and Sir protein recruitment. |
Publication Type | Journal Article |
Year of Publication | 2006 |
Authors | Tamburini BA, Carson JJ, Linger JG, Tyler JK |
Journal | Genetics |
Volume | 173 |
Issue | 2 |
Pagination | 599-610 |
Date Published | 2006 Jun |
ISSN | 0016-6731 |
Keywords | Binding Sites, Cell Cycle Proteins, Gene Silencing, Genes, Dominant, Genes, Fungal, Histones, Molecular Chaperones, Mutation, Protein Binding, Ribonucleases, Saccharomyces cerevisiae, Saccharomyces cerevisiae Proteins, Silent Information Regulator Proteins, Saccharomyces cerevisiae, Transcription, Genetic |
Abstract | Transcriptional silencing involves the formation of specialized repressive chromatin structures. Previous studies have shown that the histone H3-H4 chaperone known as chromatin assembly factor 1 (CAF-1) contributes to transcriptional silencing in yeast, although the molecular basis for this was unknown. In this work we have identified mutations in the nonconserved C terminus of antisilencing function 1 (Asf1) that result in enhanced silencing of HMR and telomere-proximal reporters, overcoming the requirement for CAF-1 in transcriptional silencing. We show that CAF-1 mutants have a drastic reduction in DNA-bound histone H3 levels, resulting in reduced recruitment of Sir2 and Sir4 to the silent loci. C-terminal mutants of another histone H3-H4 chaperone Asf1 restore the H3 levels and Sir protein recruitment to the silent loci in CAF-1 mutants, probably as a consequence of the weakened interaction between these Asf1 mutants and histone H3. As such, these studies have identified the nature of the molecular defect in the silent chromatin structure that results from inactivation of the histone chaperone CAF-1. |
DOI | 10.1534/genetics.105.054783 |
Alternate Journal | Genetics |
PubMed ID | 16582440 |
PubMed Central ID | PMC1526541 |
Grant List | R01 GM064475 / GM / NIGMS NIH HHS / United States GM64475 / GM / NIGMS NIH HHS / United States |
Related Faculty:
Jessica K. Tyler, Ph.D.