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Shep的RNA结合能力是拮抗染色质绝缘子活性所必需的。

Shep RNA-Binding Capacity Is Required for Antagonism of Chromatin Insulator Activity.

作者信息

Chen Dahong, Brovkina Margarita, Matzat Leah H, Lei Elissa P

机构信息

Nuclear Organization and Gene Expression Section, Laboratory of Cellular and Developmental Biology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, 20892.

Nuclear Organization and Gene Expression Section, Laboratory of Cellular and Developmental Biology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, 20892

出版信息

G3 (Bethesda). 2019 Mar 7;9(3):749-754. doi: 10.1534/g3.118.200923.

DOI:10.1534/g3.118.200923
PMID:30630880
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6404607/
Abstract

Chromatin insulators are DNA-protein complexes that regulate chromatin structure and gene expression in a wide range of organisms. These complexes also harbor enhancer blocking and barrier activities. Increasing evidence suggests that RNA molecules are integral components of insulator complexes. However, how these RNA molecules are involved in insulator function remains unclear. The RNA-binding protein Shep associates with the insulator complex and inhibits insulator activities. By mutating key residues in the RRM domains, we generated a Shep mutant protein incapable of RNA-binding, and this mutant lost the ability to inhibit barrier activity. In addition, we found that one of many wildtype Shep isoforms but not RRM mutant Shep was sufficient to repress enhancer blocking activities. Finally, wildtype Shep rescued synthetic lethality of , double-mutants and developmental defects of mutant neurons, whereas mutant Shep failed to do so. These results indicate that the RNA-binding ability of Shep is essential for its ability to antagonize insulator activities and promote neuronal maturation. Our findings suggest that regulation of insulator function by RNA-binding proteins relies on RNA-mediated interactions.

摘要

染色质绝缘子是一种DNA-蛋白质复合物,可调节多种生物体中的染色质结构和基因表达。这些复合物还具有增强子阻断和屏障活性。越来越多的证据表明,RNA分子是绝缘子复合物的重要组成部分。然而,这些RNA分子如何参与绝缘子功能仍不清楚。RNA结合蛋白Shep与绝缘子复合物结合并抑制绝缘子活性。通过突变RRM结构域中的关键残基,我们生成了一种无法结合RNA的Shep突变蛋白,该突变体失去了抑制屏障活性的能力。此外,我们发现许多野生型Shep异构体中的一种,但不是RRM突变体Shep,足以抑制增强子阻断活性。最后,野生型Shep挽救了 双突变体的合成致死性和 突变神经元的发育缺陷,而突变型Shep则未能做到这一点。这些结果表明,Shep的RNA结合能力对于其拮抗绝缘子活性和促进神经元成熟的能力至关重要。我们的研究结果表明,RNA结合蛋白对绝缘子功能的调节依赖于RNA介导的相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dc4/6404607/96019ecc4a88/749f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dc4/6404607/453bb68b3cb8/749f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dc4/6404607/84af6fb4e5d6/749f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dc4/6404607/ad60f35d346f/749f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dc4/6404607/96019ecc4a88/749f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dc4/6404607/453bb68b3cb8/749f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dc4/6404607/84af6fb4e5d6/749f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dc4/6404607/ad60f35d346f/749f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dc4/6404607/96019ecc4a88/749f4.jpg

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Regulatory Mechanisms of Metamorphic Neuronal Remodeling Revealed Through a Genome-Wide Modifier Screen in .
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