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基于成像的 RNA 聚合酶 II 延伸因子 Elongin 和 Elongin 泛素连接酶功能研究的检测方法。

Imaging-based assays for investigating functions of the RNA polymerase II elongation factor Elongin and the Elongin ubiquitin ligase.

机构信息

Stowers Institute for Medical Research, 1000 E 50th Street, Kansas City, MO 64110, United States.

Stowers Institute for Medical Research, 1000 E 50th Street, Kansas City, MO 64110, United States; Department of Biochemistry & Molecular Biology, University of Kansas Medical Center, Kansas City, KS 66160, United States.

出版信息

Methods. 2019 Apr 15;159-160:157-164. doi: 10.1016/j.ymeth.2019.02.015. Epub 2019 Feb 19.

Abstract

Elongin A binds to Elongins B and C to form the RNA polymerase II transcription elongation factor Elongin. It also functions as the substrate recognition subunit of a ubiquitin ligase that is formed by binding of Elongin to Cullin protein CUL5 and RING finger protein RBX2 and that targets RNA polymerase II for ubiquitination. In this article, we describe use of acceptor photobleaching fluorescence resonance energy transfer (AP-FRET) and laser microirradiation-based assays to study regulated assembly of the Elongin ubiquitin ligase and its recruitment to regions of localized DNA damage.

摘要

Elongin A 与 Elongins B 和 C 结合形成 RNA 聚合酶 II 转录延伸因子 Elongin。它还作为泛素连接酶的底物识别亚基发挥作用,该泛素连接酶由 Elongin 与 Cullin 蛋白 CUL5 和 RING 指蛋白 RBX2 结合形成,并将 RNA 聚合酶 II 作为泛素化的靶标。在本文中,我们描述了使用受体光漂白荧光共振能量转移 (AP-FRET) 和基于激光微照射的测定法来研究 Elongin 泛素连接酶的调节组装及其募集到局部 DNA 损伤区域的情况。

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