Role of WISp39 and Ubiquitination in p21 Function

WISp39 和泛素化在 p21 功能中的作用

• 批准号: 6775035
• 负责人: ARUN FOTEDAR
• 金额: $ 34.37万
• 依托单位: SIDNEY KIMMEL CANCER CENTER
• 依托单位国家: 美国
• 财政年份: 2004
• 资助国家: 美国
• 起止时间: 2004-04-09 至 2009-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6775035
• 关键词: DNA damage; RNA interference; binding proteins; cell cycle; confocal scanning microscopy; enzyme complex; enzyme mechanism; flow cytometry; genetic regulation; genetically modified animals; heat shock proteins; ionizing radiation; laboratory mouse; neoplastic growth; oncoprotein p21; posttranslational modifications; protein structure function; protooncogene; reproductive development; tissue /cell culture; ubiquitin

DESCRIPTION (provided by applicant): p21WAF1/CIP1 protein is a critical p53 transcriptional target, which is required for cell cycle arrest after ionizing radiation. The development of histiocytic sarcomas, hemangiomas/hemangiosarcomas and B cell lymphomas in p21 -/- mice suggests the importance of p21 in cancer. Loss of p21 also increases Adenomatous Polyposis Coil initiated gastrointestinal tumors, increases chemical induced skin carcinoma and cooperates with loss of other tumor suppressors like Rb and p18. p21 has also been shown to play an important role in autoimmunity and stem cell repopulation. It is therefore critical that we understand the regulatory pathways which control p21 protein levels. Although numerous studies have investigated the importance of transcriptional regulation in p21 function, the role of post translational regulation remains less clear. The regulation of p21 proteins levels by post translational mechanisms is the focus of this grant. In preliminary results we describe the identification of a novel protein WISp39 (p39) which stabilizes p21 protein levels. WISp39 acts like an adaptor protein which recruits Hsp90 (via its C-terminal TPR domain) in order to stabilize p21. We propose to investigate in detail the role of Hsp90 binding TPR proteins in regulating p21 stability and function. We will analyze the molecular and functional characteristics of p39 mediated p21 stability using both tissue culture models and whole animal models. By generating p39 -/- mice we will evaluate the functional consequences of p39 on p21 stability in checkpoint control, and tumor generation and development in a whole animal model. Finally we will study the effect of non-ubiquitinated p21 on cell cycle and the cellular response to DNA damage.

描述（申请人提供）：p21 WAF 1/CIP 1蛋白是一种关键的p53转录靶点，是电离辐射后细胞周期阻滞所必需的。p21 -/-小鼠中组织细胞肉瘤、血管瘤/血管瘤和B细胞淋巴瘤的发展表明p21在癌症中的重要性。 p21的缺失也增加腺瘤性息肉病线圈引发的胃肠道肿瘤，增加化学诱导的皮肤癌，并与其他肿瘤抑制因子如Rb和p18的缺失协同作用。p21还显示在自身免疫和干细胞再增殖中起重要作用。 因此，我们必须了解控制p21蛋白水平的调控途径。虽然许多研究已经研究了转录调控在p21功能中的重要性，但翻译后调控的作用仍然不太清楚。通过翻译后机制调节p21蛋白水平是该资助的重点。 在初步结果中，我们描述了一种新的蛋白质WISp 39（p39），稳定p21蛋白水平的鉴定。WISp 39的作用类似于一个衔接蛋白，它募集Hsp 90（通过其C-末端TPR结构域）以稳定p21。我们建议详细研究热休克蛋白90结合TPR蛋白在调节p21的稳定性和功能的作用。 我们将使用组织培养模型和整体动物模型分析p39介导的p21稳定性的分子和功能特征。通过产生p39 -/-小鼠，我们将评估p39在检查点控制中对p21稳定性的功能后果，以及在整个动物模型中的肿瘤产生和发展。最后，我们将研究非泛素化p21对细胞周期和细胞对DNA损伤的反应的影响。