Cotranscriptional Set2 methylation of histone H3 lysine 36 recruits a repressive Rpd3 complex

被引:640
作者
Keogh, MC
Kurdistani, SK
Morris, SA
Ahn, SH
Podolny, V
Collins, SR
Schuldiner, M
Chin, KY
Punna, T
Thompson, NJ
Boone, C
Emili, A
Weissman, JS
Hughes, TR
Strahl, BD
Grunstein, M
Greenblatt, JF
Buratowski, S
Krogan, NJ
机构
[1] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Dept Biol Chem, Los Angeles, CA 90095 USA
[3] Univ N Carolina, Sch Med, Dept Biochem & Biophys, Chapel Hill, NC 27599 USA
[4] Univ Calif San Francisco, Howard Hughes Med Inst, Dept Cellular & Mol Pharmacol, San Francisco, CA 94143 USA
[5] Univ Toronto, Banting & Best Dept Med Res, Toronto, ON M5G 1L6, Canada
[6] Univ Toronto, Dept Med Genet & Microbiol, Toronto, ON M5S 1A8, Canada
基金
美国国家卫生研究院; 加拿大健康研究院;
关键词
D O I
10.1016/j.cell.2005.10.025
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The yeast histone deacetylase Rpd3 can be recruited to promoters to repress transcription initiation. Biochemical, genetic, and gene-expression analyses show that Rpd3 exists in two distinct complexes. The smaller complex, Rpd3C(S), shares Sin3 and Ume1 with Rpd3C(L) but contains the unique subunits Rco1 and Eaf3. Rpd3C(S) mutants exhibit phenotypes remarkably similar to those of Set2, a histone methyltransferase associated with elongating RNA polymerase II. Chromatin immunoprecipitation and biochemical experiments indicate that the chromodomain of Eaf3 recruits Rpd3C(S) to nucleosomes methylated by Set2 on histone H3 lysine 36, leading to deacetylation of transcribed regions. This pathway apparently acts to negatively regulate transcription because deleting the genes for Set2 or Rpd3C(S) bypasses the requirement for the positive elongation factor Bur1/ Bur2.
引用
收藏
页码:593 / 605
页数:13
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