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额外性梳蛋白与zeste增强子和三体胸苷相互作用,并在热休克蛋白70(hsp70)转录过程中调节组蛋白H3K4和H3K27上的三甲基化水平。

Additional sex combs interacts with enhancer of zeste and trithorax and modulates levels of trimethylation on histone H3K4 and H3K27 during transcription of hsp70.

作者信息

Li Taosui, Hodgson Jacob W, Petruk Svetlana, Mazo Alexander, Brock Hugh W

机构信息

Department of Zoology, Life Sciences Institute, University of British Columbia, 2350 Health Science Mall, Vancouver, BC, V6T 1Z4, Canada.

Department of Biochemistry and Molecular Biology, Thomas Jefferson University, Philadelphia, PA, 19107, USA.

出版信息

Epigenetics Chromatin. 2017 Sep 19;10(1):43. doi: 10.1186/s13072-017-0151-3.

Abstract

BACKGROUND

Maintenance of cell fate determination requires the Polycomb group for repression; the trithorax group for gene activation; and the enhancer of trithorax and Polycomb (ETP) group for both repression and activation. Additional sex combs (Asx) is a genetically identified ETP for the Hox loci, but the molecular basis of its dual function is unclear.

RESULTS

We show that in vitro, Asx binds directly to the SET domains of the histone methyltransferases (HMT) enhancer of zeste [E(z)] (H3K27me3) and Trx (H3K4me3) through a bipartite interaction site separated by 846 amino acid residues. In Drosophila S2 cell nuclei, Asx interacts with E(z) and Trx in vivo. Drosophila Asx is required for repression of heat-shock gene hsp70 and is recruited downstream of the hsp70 promoter. Changes in the levels of H3K4me3 and H3K27me3 downstream of the hsp70 promoter in Asx mutants relative to wild type show that Asx regulates H3K4 and H3K27 trimethylation.

CONCLUSIONS

We propose that during transcription Asx modulates the ratio of H3K4me3 to H3K27me3 by selectively recruiting the antagonistic HMTs, E(z) and Trx or other nucleosome-modifying enzymes to hsp70.

摘要

背景

细胞命运决定的维持需要多梳蛋白组进行抑制;三体胸蛋白组进行基因激活;以及三体胸蛋白和多梳蛋白增强子(ETP)组进行抑制和激活。额外性梳(Asx)是一种通过遗传学方法鉴定出的针对Hox基因座的ETP,但尚不清楚其双重功能的分子基础。

结果

我们发现,在体外,Asx通过一个由846个氨基酸残基隔开的二分相互作用位点,直接与组蛋白甲基转移酶(HMT)zeste增强子[E(z)](H3K27me3)和Trx(H3K4me3)的SET结构域结合。在果蝇S2细胞核中,Asx在体内与E(z)和Trx相互作用。果蝇Asx是热休克基因hsp70抑制所必需的,并被招募到hsp70启动子下游。相对于野生型,Asx突变体中hsp70启动子下游H3K4me3和H3K27me3水平的变化表明,Asx调节H3K4和H3K27的三甲基化。

结论

我们提出,在转录过程中,Asx通过选择性地将拮抗的HMT、E(z)和Trx或其他核小体修饰酶招募到hsp70,来调节H3K4me3与H3K27me3的比例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed97/5605996/f21b1f4a58aa/13072_2017_151_Fig1_HTML.jpg

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