Different Ezh2-containing complexes target methylation of histone H1 or nucleosomal histone H3

被引:376
作者
Kuzmichev, A
Jenuwein, T
Tempst, P
Reinberg, D [1 ]
机构
[1] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Howard Hughes Med Inst, Piscataway, NJ 08854 USA
[2] Univ Med & Dent New Jersey, Div Nucleic Acids Enzymol, Dept Biochem, Piscataway, NJ 08854 USA
[3] Vienna Bioctr, Res Inst Mol Pathol, A-1030 Vienna, Austria
[4] Mem Sloan Kettering Canc Ctr, Program Mol Biol, New York, NY 10021 USA
关键词
D O I
10.1016/S1097-2765(04)00185-6
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
Human Enhancer of Zeste homolog (Ezh2) is a histone lysine methyltransferase (HKMT) associated with transcriptional repression. Ezh2 is present in several distinct complexes, one of which, PRC2, we characterized previously. Here we report an additional Ezh2 complex, PRC3. We show that the Ezh2 complexes exhibit differential targeting of specific histories for lysine methylation dependent upon the context of the histone substrates. This differential targeting is a function of the associated Eed protein within each complex. We found that Eed protein is present in four isoforms, which represent alternate translation start site usage from the same mRNA. These Eed isoforms selectively associate with distinct Ezh2-containing complexes with resultant differential targeting of their associated HKMT activity toward histone H3-K27 or histone H1-K26. Our data provide evidence for a novel mechanism regulating the substrate specificity of a chromatin-modifying enzyme through disparate translational products of a regulatory subunit.
引用
收藏
页码:183 / 193
页数:11
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