FACT facilitates transcription-dependent nucleosome alteration

被引:662
作者
Belotserkovskaya, R
Oh, S
Bondarenko, VA
Orphanides, G
Studitsky, VM
Reinberg, D [1 ]
机构
[1] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Howard Hughes Med Inst, Dept Biochem,Div Nucl Acids enzymol, Piscataway, NJ 08854 USA
[2] Wayne State Univ, Sch Med, Dept Biochem, Detroit, MI 48201 USA
关键词
D O I
10.1126/science.1085703
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The FACT (facilitates chromatin transcription) complex is required for transcript elongation through nucleosomes by RNA polymerase II (Pol II) in vitro. Here, we show that FACT facilitates Pol II-driven transcription by destabilizing nucleosomal structure so that one histone H2A-H2B dimer is removed during enzyme passage. We also demonstrate that FACT possesses intrinsic histone chaperone activity and can deposit core histones onto DNA. Importantly, FACT activity requires both of its constituent subunits and is dependent on the highly acidic C terminus of its larger subunit, Spt16. These findings define the mechanism by which Pol II can transcribe through chromatin without disrupting its epigenetic status.
引用
收藏
页码:1090 / 1093
页数:4
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