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Brd4 and JMJD6-associated anti-pause enhancers in regulation of transcriptional pause release.

Cell. 2013; 
LiuWen,MaQi,WongKaki,LiWenbo,OhgiKenny,ZhangJie,AggarwalAneel,RosenfeldMicha
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Peptide Synthesis Biotinylated histone peptides used in this study were purchased from Millipore or custom synthesized by GenScript ... tetra-acetylated Histone H4 (K5, 8, 12 and 16) (H4Ac) (Millipore, 12-379); di-acetylated Histone H3 (K9 and 14) (H3Ac) (Millipore, 12-402); unmodified histone H4 (K5, 8, 12 and 16) (GenScript); unmodified histone H3 (K9 and 14) (GenScript); H4R3me1, H4R3me2 (a) and H4R3me2 (s) (GenScript, SGRGKGGKGL GKGGAKRH) Get A Quote

摘要

Distal enhancers characterized by the H3K4me(1) mark play critical roles in developmental and transcriptional programs. However, potential roles of specific distal regulatory elements in regulating RNA polymerase II (Pol II) promoter-proximal pause release remain poorly investigated. Here, we report that a unique cohort of jumonji C-domain-containing protein 6 (JMJD6) and bromodomain-containing protein 4 (Brd4) cobound distal enhancers, termed anti-pause enhancers (A-PEs), regulate promoter-proximal pause release of a large subset of transcription units via long-range interactions. Brd4-dependent JMJD6 recruitment on A-PEs mediates erasure of H4R3me(2(s)), which is directly read by 7SK snRNA, and de... More

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