Role of ribosomal proteins in regulating c-Myc

核糖体蛋白在调节 c-Myc 中的作用

• 批准号: 7643954
• 负责人: Hua Lu
• 金额: $ 31.33万
• 依托单位: INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-07-01 至 2013-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7643954
• 关键词: Address; Affect; Animal Model; Binding; Biogenesis; Biological Assay; Biological Models; Boxing; Cell Nucleolus; Cell Proliferation; Cells; Chromatin; Complex; Feedback; Gene Targeting; Genetic Transcription; Goals; Human; Immunoprecipitation; Lead; Light; Malignant Neoplasms; Mediating; Messenger RNA; Molecular; Oncogene Proteins; Phase; Physiological; Play; Polymerase; Production; Proteins; Proto-Oncogene Proteins c-myc; RNA Polymerase I; Recruitment Activity; Regulation; Ribosomal Proteins; Ribosomes; Role; Serum; Small Interfering RNA; Staging; Stress; TRRAP gene; Transactivation; Transcription Coactivator; Up-Regulation; antitumor drug; c-myc Genes; cell growth; cell transformation; cofactor; human DICER1 protein; inhibitor/antagonist; insight; mRNA Stability; overexpression; prevent; promoter; public health relevance; response; ribosomal protein L11; tumorigenesis

DESCRIPTION (provided by applicant): Our long-term goal is to understand the roles of ribosomal proteins in regulating c-Myc activity during ribosomal biogenesis and in preventing c-Myc-induced cancer formation. In this proposal, we will dissect the L11-c-Myc auto-regulatory feedback loop and its implication in repressing cell transformation. c-Myc promotes cell growth by enhancing ribosomal biogenesis mediated by RNA polymerases I, II and III. Overexpression of c-Myc and aberrant ribosomal biogenesis lead to deregulated cell growth and contribute to tumorigenesis. High levels of c-Myc associate with ~80% of various human cancers. Thus, c-Myc must be tightly controlled in cells. Recently, we have identified ribosomal protein L11, a component of the large subunit of the ribosome, as a likely feedback regulator of c-Myc. L11 is transcriptionally induced by c-Myc. But, overexpression of L11 inhibits c-Myc-dependent transactivation and cell proliferation. L11 directly binds to the Myc box II (MBII) motif within the transactivational domain (TAD) of c-Myc and is recruited to c-Myc target promoters by this transcriptional activator, consequently inhibiting the association of one of the c-Myc coactivators, TRRAP, which also binds to MBII, with c-Myc at these promoters. Furthermore, knockdown of endogenous L11 by siRNA increases c-Myc mRNA and protein levels as well as its activity. Finally, L11 is crucial for the later stage reduction of endogenous c-Myc levels and the late phase inhibition of its activity in response to serum stimulation. In light of these exciting findings, I hypothesize that L11 may act as an auto-regulatory feedback inhibitor of c-Myc, playing a physiological role in negatively regulating c-Myc-enhanced cell proliferation and tumorigenesis. Hence, we will systematically investigate this previously untested hypothesis by addressing three specific aims: (1). Dissect molecular mechanisms underlying L11 inhibition of c-Myc-dependent transcription; (2). Elucidate how L11 regulates c-Myc protein and mRNA levels; (3). Determine the physiological significance of L11-c-Myc inhibitory feedback regulation in cell and animal model systems. These studies will offer new molecular insight into the regulation of c-Myc during ribosomal biogenesis and reveal a potential role of L11 in preventing c-Myc-induced tumorigenesis. Also, these studies will provide important information for developing anti-tumor drugs that inhibit c-Myc and thus are likely useful for treating cancers harboring high levels of active c-Myc. PUBLIC HEALTH RELEVANCE: My proposed studies will offer new molecular insight into the regulation of the c-Myc oncoprotein during de novo protein production, and reveal a potential role of the ribosomal protein L11 in preventing c-Myc-induced cancer formation, as c-Myc is highly expressed in more than 80% of human cancers. Also, these studies will provide important information for developing anti-tumor drugs that inhibit c-Myc and thus are likely useful for treating cancers harboring high levels of active c-Myc.

描述(由申请人提供)：我们的长期目标是了解核糖体蛋白在核糖体生物发生过程中调节c-Myc活性和防止c-Myc诱导的癌症形成中的作用。在这项提案中，我们将剖析L11-c-Myc自动调节反馈环及其在抑制细胞转化中的意义。C-Myc通过促进RNA聚合酶I、II和III介导的核糖体生物合成促进细胞生长。c-Myc的过度表达和异常的核糖体生物合成导致细胞生长失控并促进肿瘤的发生。高水平的c-Myc与约80%的各种人类癌症有关。因此，c-Myc必须在细胞内受到严格控制。最近，我们已经确定核糖体蛋白L11是核糖体大亚基的一个组成部分，可能是c-Myc的反馈调节因子。L11在转录水平上受c-Myc诱导。但是，L11的过表达抑制了c-Myc依赖的反式激活和细胞增殖。L11直接与c-Myc反式激活结构域(TAD)内的Myc box II(MBII)基序结合，并被该转录激活子招募到c-Myc靶启动子，从而抑制c-Myc共激活子之一TRRAP(也与MBII结合)与这些启动子上的c-Myc的结合。此外，siRNA下调内源性L11基因可增加c-Myc的mRNA和蛋白水平及其活性。最后，L11在内源性c-Myc水平的后期降低和对血清刺激反应的后期活性抑制中起关键作用。根据这些令人兴奋的发现，我推测L11可能作为c-Myc的自我调节反馈抑制物，在负调控c-Myc增强的细胞增殖和肿瘤发生中发挥生理作用。因此，我们将通过解决三个具体目标来系统地研究这一先前未经检验的假说：(1)。剖析L11抑制c-Myc依赖转录的分子机制；阐明L11是如何调节c-Myc蛋白和mRNA水平的；确定L11-c-Myc抑制性反馈调节在细胞和动物模型系统中的生理意义。这些研究将为c-Myc在核糖体生物发生过程中的调控提供新的分子视角，并揭示L11在预防c-Myc诱导的肿瘤发生中的潜在作用。此外，这些研究将为开发抑制c-Myc的抗肿瘤药物提供重要信息，从而可能有助于治疗含有高水平活性c-Myc的癌症。公共卫生相关性：我提出的研究将为c-Myc癌蛋白在从头蛋白产生过程中的调控提供新的分子见解，并揭示核糖体蛋白L11在防止c-Myc诱导的癌症形成方面的潜在作用，因为c-Myc在80%以上的人类癌症中高度表达。此外，这些研究将为开发抑制c-Myc的抗肿瘤药物提供重要信息，从而可能有助于治疗含有高水平活性c-Myc的癌症。