DNA REPAIR SIGNALING BY NOVEL POLYUBIQUITIN CHAINS

新型多泛素链的 DNA 修复信号传导

• 批准号: 6498710
• 负责人: Cecile M. Pickart
• 金额: $ 27.76万
• 依托单位: JOHNS HOPKINS UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2000
• 资助国家: 美国
• 起止时间: 2000-02-01 至 2004-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6498710
• 关键词: DNA binding protein; DNA repair; affinity chromatography; biological signal transduction; fungal proteins; genetic library; protein protein interaction; proteolysis; ubiquitin

Polyubiquitin (polyUb) chains linked through lysine-48 (K48) of Ub represent the predominant targeting signal in the Ub-proteasome proteolytic pathway, whereas polyUb chains linked through K63 function in postreplicative DNA repair by a mechanism which does not appear to involve proteolysis. These observations suggest that the assembly of Ub into distinct types of polymers may be a mechanism to diversify the signaling functions of Ub. To test this hypothesis we will apply methods of biochemistry and yeast molecular genetics to characterize the assembly and recognition of K63-linked polyUb chains, and elucidate the signaling function of these polymers in DNA repair. Our discovery of yeast enzymes which assemble homopolymeric K63-linked polyUb chains in vitro, and function in DNA repair in vivo, provides the starting point for this work. These proteins are Ubcl3p (a Ub conjugating enzyme) and Mms2p (a Ub E2 variant or UEV protein). By characterizing the mechanism and function of the Mms2p/Ubc13p complex, we will explicate the process of signal generation; by identifying cellular proteins that are linked to K63-linked chains, we will gain insight into the functional consequences of signal recognition; finally, by using an in vitro-assembled chain as a tool, we will directly address the proteolytic signaling competence of K63-linked polyUb chains, and isolate chain-recognizing factors that may represent downstream elements in the proposed DNA repair signaling pathway. The results of these studies will provide new insights into the mechanistic role of Ub in DNA repair, and may ultimately lead to improved strategies for the treatment of cancer and other diseases. Moreover, if our results support the hypothesis that polyUb chains serve to diversify the signaling functions of Ub, it will help to explain how this small molecule is able to act as a distinct signal in multiple cellular processes. Finally, our results will provide the first biochemical insight into the functioning of UEV protein family, which in mammals includes the tumor suppressor Tsgl0l, and other proteins implicated in differention and cell transformation.

通过UB的赖氨酸-48（K48）连接的多泛素（Polyub）链代表UB--蛋白酶体蛋白水解途径中的主要靶向信号，而通过在呼吸息DNA中通过K63功能链接的Polyub链，该机制似乎不涉及蛋白质溶解的机制。这些观察结果表明，将UB组装成不同类型的聚合物可能是使UB信号传导功能多样化的机制。为了检验这一假设，我们将应用生物化学和酵母分子遗传学方法来表征K63连接的多核链的组装和识别，并阐明这些聚合物在DNA修复中的信号传导功能。我们发现的酵母酶在体外聚集了均聚糖K63连接的多核链，并在体内DNA修复中的功能为这项工作提供了起点。这些蛋白质是UBCL3P（UB共轭酶）和MMS2P（UB E2变体或UEV蛋白）。通过表征MMS2P/UBC13P复合物的机制和功能，我们将解释信号生成过程。通过鉴定与K63连锁链相关的细胞蛋白，我们将深入了解信号识别的功能后果。最后，通过使用体外组装链作为工具，我们将直接解决K63链接的多蛋白链的蛋白水解信号传导能力，以及分离链链识别因子，这些因子可能代表提议的DNA修复信号通路中下游元素。这些研究的结果将为UB在DNA修复中的机械作用提供新的见解，并最终可能会改善治疗癌症和其他疾病的策略。此外，如果我们的结果支持多元链来多样化UB的信号传导功能的假设，则将有助于解释该小分子如何在多个细胞过程中充当独特的信号。最后，我们的结果将为UEV蛋白家族的功能提供第一个生化见解，在哺乳动物中包括肿瘤抑制剂TSGL0L，以及与差异和细胞转化有关的其他蛋白质。