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The ROC-Cullin Family of E3 Ubiquitin Ligases

The ROC-Cullin Family of E3 Ubiquitin Ligases
E3 泛素连接酶的 ROC-Cullin 家族
批准号:
6698097
负责人:
YUE XIONG
金额:
$26.0万
依托单位国家:
美国
项目类别:
财政年份:
2003
资助国家:
美国
项目状态:
已结题
起止时间:
2003-02-01 至 2007-01-31

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中文摘要
翻译
描述(申请人提供):库林斯是最近发现的一个进化保守的蛋白质家族,与潜在的大量细胞蛋白质的泛素化有关。对少数库林斯的研究表明,库林斯在细胞周期和细胞生长控制、肿瘤抑制和动物发育等不同的生理过程中具有重要功能。我们和其他人之前发现了一种与cullin相互作用的环指蛋白ROc1(也称为Rbx1或Hrt1),它对CUL1介导的SCF E3连接酶和细胞周期进程具有必不可少的功能。我们发现,在体内,ROC1及其同系物ROC2通过变构激活E2,并与所有cullin成员相互作用,形成许多不同的ROC-cullin泛素连接酶。我们最近发现了ROC-cullin连接酶与两个进化上保守的蛋白质p120TIP120和p127DDB1之间的新相互作用。我们的初步研究表明,DDB 1可能作为依赖ROC的E3 NEDD8连接酶对cullin蛋白起作用,而TIP120蛋白可能作为多种ROC-cullin连接酶的组装因子。我们建议在哺乳动物和裂解酵母细胞中结合生化、蛋白质组学和遗传学方法进行研究,以确定TIP120和DDB 1以及特征不佳的CUL4的机制和功能。通过这些共同努力,我们期待着有机会更好地了解ROC-cullin泛素连接酶家族的调控机制,以及该E3连接酶家族识别底物的机制。 目的I.TIP120的功能和机制1.NEDD8途径对TIP120-cullin结合的调节。裂解酵母TIP120的遗传分析3.TIP120在哺乳动物细胞中体内功能的测定4.TIP120复合体的纯化和分析AIM II.DDB1作为NEDD8 E3连接酶的功能NEDD8连接的生化重组2。裂解酵母中DDB_1的遗传分析--Ⅲ.CUL4A1的功能和复合体人CUL4A2功能的测定。Cl4在分裂酵母中的功能分析3。Cl4络合物的提纯与表征。
英文摘要
DESCRIPTION (provided by applicant): Cullins are a recently identified family of evolutionarily conserved proteins linked to the ubiquitination of a potentially large number of cellular proteins. Characterization of a small number of cullins has identified critical functions in such diverse physiological processes as cell cycle and cell growth control, tumor suppression and animal development. We and others previously discovered a cullin-interacting RING finger protein, ROC1 (also known as Rbx1 or Hrt1), that carries essential function for CUL1-mediated SCF E3 ligases and for cell cycle progression. We have found that ROC1 and its homologue, ROC2, allosterically activates E2 and interacts with all cullin members to constitute many distinct ROC-cullin ubiquitin ligases in vivo. We have recently identified novel interactions between ROC-cullin ligases and two evolutionarily conserved proteins, p 120 TIP120 and p 127 DDB1. Our preliminary studies have led to the hypothesis that DDB 1 may function as a ROC-dependent E3 NEDD8 ligase toward cullin proteins, and that TIP120 proteins may function as assembly factors of various ROC-cullin ligases. We propose an investigation that combines biochemical, proteomic and genetic approaches in mammalian and fission yeast cells to determine the mechanisms and functions of TIP120 and DDB 1 and a poorly characterized CUL4. Through these concerted efforts, we anticipate a great opportunity to better understand the mechanism regulating the ROC-cullin family of ubiquitin ligases and the mechanism underlying the substrate recognition by this family of E3 ligases. Aim I. The function and mechanism of TIP120 1. Regulation of TIP120-cullin association by NEDD8 pathway in vivo2. Genetic analysis of fission yeast TIP120 3. Determination of the in vivo function of TIP120 in mammalian cells 4. Purification and analysis of TIP120 complexes.Aim II. Function of DDB1 as an NEDD8 E3 ligase.1. Biochemical reconstitution of NEDD8 ligation2. Genetic analysis of DDB 1 in fission yeastAim III. Function and complexes of CUL4A1. Determination of the function of human CUL4A2. Functional analysis of CUL4 in fission yeast3. Purification and characterization of CUL4 complexes.
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