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The Regulation of DNA Repair by Anchored and Unanchored Ubiquitin Chains

锚定和非锚定泛素链对 DNA 修复的调节

基本信息

批准号：
8253247
负责人：
Miklos Bekes
金额：
$ 4.92万
依托单位：
NEW YORK UNIVERSITY SCHOOL OF MEDICINE
依托单位国家：
美国
项目类别：
财政年份：
2012
资助国家：
美国
起止时间：
2012-01-12 至 2014-09-11
项目状态：
已结题

项目摘要

Project Summary/Abstract Background: There is a considerable amount of evidence documenting the importance of ubiquitin conjugation and deconjugation in DNA repair mechanisms, as well as the identity of some the ubiquitin ligases and some of the deubiquitinating enzymes involved. However, the substrates of ubiquitination are still largely controversial and the heterogeneity of the ubiquitin chains involved has not been clearly defined. Recently, unanchored ubiquitin chains have emerged as functional regulators of innate immunity and kinase regulation, however they have not yet been addressed in DNA repair mechanisms. It is important to understand the complete picture of the "ubiquitin architecture" of DNA repair mechanisms and exploring the functional importance of unanchored ubiquitin chains presents a hitherto overlooked opportunity. Objective: The goal of this proposal is to further characterize the "ubiquitin architecture" of DNA repair mechanisms in order to be able to exploit them for more successful therapeutic strategies. On the one hand, the possibility of free, unanchored ubiquitin chains will be assessed, as well as the effect of sustained ubiquitin chain formation on DNA repair mechanisms, both of which will underscore the importance of deubiquitinating enzymes (DUBs) as crucial regulators of DNA repair pathways. Specific Aims: (1) Determine the existence and abundance of unanchored ubiquitin chains during DNA damage responses, (2) Determine the effect of sustained ubiquitin chain formation on DNA damage responses, (3) Identify functionally important interacting proteins of alternative ubiquitin-linkages within DNA damage foci. Study Design: At first, polyubiquitin conjugates will be purified from cells treated by DNA damaging agents and ubiquitin conjugates will be assessed for their free ubiquitin chain content. Then, the effect of a conjugation- competent but deconjugation-deficient mutant of ubiquitin that I have recently developed will be tested to initiate a DNA repair response mechanism in the absence of DNA damage. Additionally, the effect of the mutant in making ubiquitin chains of a defined linkage will be tested under DNA damaging conditions to see if sustained ubiquitin chain formation sensitizes cells to DNA damage or inhibits the response. Finally, ubiquitin chain binding proteins will be purified by affinity purification from DNA damage induced cells to identify novel interacting proteins of alternative ubiquitin chains involved in DNA damage by mass spectrometry.

项目总结/摘要工作背景：有大量的证据证明了泛素结合和解结合在DNA修复机制中的重要性，以及一些泛素连接酶和一些涉及的去泛素化酶的身份。然而，泛素化的底物仍然存在很大的争议，所涉及的泛素链的异质性尚未明确定义。最近，未锚定的泛素链已成为先天免疫和激酶调节的功能调节剂，但它们尚未在DNA修复机制中得到解决。了解DNA修复机制的“泛素结构”的全貌是很重要的，探索未锚定的泛素链的功能重要性是迄今为止被忽视的机会。目的：该提案的目标是进一步表征DNA修复机制的“泛素结构”，以便能够利用它们来实现更成功的治疗策略。一方面，将评估游离的、未锚定的泛素链的可能性，以及持续的泛素链形成对DNA修复机制的影响，这两者都将强调去泛素化酶（DUBs）作为DNA修复途径的关键调节剂的重要性。具体目标：（1）确定DNA损伤反应中未锚定的泛素链的存在和丰度，（2）确定持续的泛素链形成对DNA损伤反应的影响，（3）鉴定DNA损伤灶内替代泛素连接的功能重要的相互作用蛋白。研究设计：首先，将从DNA损伤剂处理的细胞中纯化聚泛素缀合物，并评估泛素缀合物的游离泛素链含量。然后，将测试我最近开发的具有缀合能力但去缀合缺陷的泛素突变体在没有DNA损伤的情况下启动DNA修复反应机制的作用。此外，将在DNA损伤条件下测试突变体在形成具有限定连接的泛素链中的作用，以观察持续的泛素链形成是否使细胞对DNA损伤敏感或抑制反应。最后，将通过亲和纯化从DNA损伤诱导的细胞中纯化泛素链结合蛋白，以通过质谱鉴定参与DNA损伤的替代泛素链的新型相互作用蛋白。