Cell cycle-regulated histone acetylation required for expression of the yeast HO gene

被引:239
作者
Krebs, JE
Kuo, MH
Allis, CD
Peterson, CL [1 ]
机构
[1] Univ Massachusetts, Med Ctr, Program Mol Med, Worcester, MA 01605 USA
[2] Univ Massachusetts, Med Ctr, Dept Biochem & Mol Biol, Worcester, MA 01605 USA
[3] Univ Virginia, Sch Med, Dept Biochem, Charlottesville, VA 22906 USA
关键词
cell cycle; yeast; HO gene; histone acetylation; chromatin remodeling;
D O I
10.1101/gad.13.11.1412
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Expression of the yeast HO gene in late G(1) of the cell cycle requires the SWI/SNF chromatin remodeling complex, the Gcn5p histone acetyltransferase, and two different sequence-specific transcriptional activators, Swi5p and Swi4p/Swi6p. We have used chromatin immunoprecipitation assays to investigate the role of each of these trans-acting factors in establishing a cell cycle-regulated domain of histone acetylation surrounding the HO upstream regulatory region. We detect a similar to 1-kb domain of H3 and H4 acetylation that is established in mid-G(1), prior to and independent of HO transcription, which then declines with kinetics similar to inactivation of HO. This cell cycle burst of histone acetylation requires Gcn5p, SWI/SNF, and the Swi5p activator, but occurs in the absence of the Swi4p activator. We also find that inactivation of the Sin3p/Rpd3p deacetylase complex leads to a high level of acetylation at the HO locus throughout the cell cycle. We propose a sequential model for activation of HO in which the Swi5p-dependent recruitment of the Gcn5p acetyltransferase requires chromatin remodeling events by the SWI/SNF complex.
引用
收藏
页码:1412 / 1421
页数:10
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