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NURF301 有助于吉普赛染色体绝缘子介导的核组织。

NURF301 contributes to gypsy chromatin insulator-mediated nuclear organization.

机构信息

Nuclear Organization and Gene Expression Section, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD, USA.

Laboratory of Biochemistry and Genetics, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD, USA.

出版信息

Nucleic Acids Res. 2022 Aug 12;50(14):7906-7924. doi: 10.1093/nar/gkac600.

Abstract

Chromatin insulators are DNA-protein complexes that can prevent the spread of repressive chromatin and block communication between enhancers and promoters to regulate gene expression. In Drosophila, the gypsy chromatin insulator complex consists of three core proteins: CP190, Su(Hw), and Mod(mdg4)67.2. These factors concentrate at nuclear foci termed insulator bodies, and changes in insulator body localization have been observed in mutants defective for insulator function. Here, we identified NURF301/E(bx), a nucleosome remodeling factor, as a novel regulator of gypsy insulator body localization through a high-throughput RNAi imaging screen. NURF301 promotes gypsy-dependent insulator barrier activity and physically interacts with gypsy insulator proteins. Using ChIP-seq, we found that NURF301 co-localizes with insulator proteins genome-wide, and NURF301 promotes chromatin association of Su(Hw) and CP190 at gypsy insulator binding sites. These effects correlate with NURF301-dependent nucleosome repositioning. At the same time, CP190 and Su(Hw) both facilitate recruitment of NURF301 to chromatin. Finally, Oligopaint FISH combined with immunofluorescence revealed that NURF301 promotes 3D contact between insulator bodies and gypsy insulator DNA binding sites, and NURF301 is required for proper nuclear positioning of gypsy binding sites. Our data provide new insights into how a nucleosome remodeling factor and insulator proteins cooperatively contribute to nuclear organization.

摘要

染色质绝缘子是一种 DNA-蛋白质复合物,可以防止抑制性染色质的扩散,并阻断增强子和启动子之间的通讯,从而调节基因表达。在果蝇中,gypsy 染色质绝缘子复合物由三个核心蛋白组成:CP190、Su(Hw)和 Mod(mdg4)67.2。这些因子集中在称为绝缘子体的核焦点中,并且在绝缘子功能缺陷的突变体中观察到绝缘子体定位的变化。在这里,我们通过高通量 RNAi 成像筛选鉴定出 NURF301/E(bx),一种核小体重塑因子,作为 gypsy 绝缘子体定位的新调节因子。NURF301 促进 gypsy 依赖的绝缘子屏障活性,并与 gypsy 绝缘子蛋白发生物理相互作用。使用 ChIP-seq,我们发现 NURF301 在全基因组范围内与绝缘子蛋白共定位,并且 NURF301 促进 Su(Hw)和 CP190 在 gypsy 绝缘子结合位点处的染色质关联。这些效应与 NURF301 依赖的核小体重定位相关。同时,CP190 和 Su(Hw)都有助于 NURF301 募集到染色质上。最后,Oligopaint FISH 结合免疫荧光显示,NURF301 促进了绝缘子体和 gypsy 绝缘子 DNA 结合位点之间的 3D 接触,并且 NURF301 是 gypsy 结合位点正确核定位所必需的。我们的数据提供了新的见解,即核小体重塑因子和绝缘子蛋白如何协同作用于核组织。

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