Structural Biology of the Sin3 Corepressor Complex

描述（由申请人提供）：真核生物基因表达在转录水平的调控依赖于多种蛋白因子的协同作用。序列特异性DNA结合因子和染色质结合蛋白将含有染色质修饰活性的多亚基共调节复合物募集到基因组上的特定位点是调控基因转录的重要步骤。Sin3辅抑制因子复合体是迄今为止在哺乳动物细胞中发现的少数主要辅抑制因子复合体之一。这种复合物对基因转录的负面影响部分依赖于核组蛋白去乙酰化酶（hdac）的作用，hdac是一组催化乙酰化染色质底物中乙酰基水解的酶。~150 kDa的Sin3蛋白既可以作为辅助抑制因子复合物组装的分子支架，也可以直接或间接地通过复合物的其他组分与数量庞大且种类繁多的dna结合转录因子和染色质结合蛋白相互作用，这些转录因子和染色质结合蛋白在正常生长、发育和细胞稳态中发挥重要作用。我们下一个资助期的研究将广泛地解决Sin3共抑制因子复合体的组分如何被不同的启动子结合转录因子和翻译后修饰组蛋白（也称为“染色质标记”）的特定模式所招募的问题。另一个主要问题是如何组装复合体以及它如何促进其功能多样性。这些问题的答案依赖于结构-功能分析。结构研究的主要工具将是溶液态核磁共振波谱，因为它非常适合研究转录因子，因为它们经常含有天然未折叠的片段，也因为所研究的系统相对较小且易于处理。此外，该技术非常适合于弱相互作用的研究，如涉及染色质结合模块的研究。功能分析将依赖于各种生化和生物物理方法。该项目的目标大致集中在三个主题上：(1)启动子结合转录因子募集Sin3共阻遏子；(2)募集和靶向特定染色质标记的共阻遏子复合体；(3)核心共阻遏子复合体的组装。公共卫生相关性：真核生物基因转录为信使rna，随后翻译产生蛋白质是由一类称为转录共调节剂的蛋白质调节的。这些共调节因子通过特异性结合DNA的蛋白质和/或结合组蛋白的蛋白质被招募到基因组的特定区域。涉及Sin3共调节因子的分子相互作用和涉及与Sin3相互作用的组蛋白结合蛋白的分子相互作用是本研究的重点，因为对这些蛋白的功能知之甚少，因为这些蛋白的缺陷和异常量与癌症等疾病有关。这项工作将试图获得在与Sin3相互作用的行为中捕获的蛋白质的详细分子图像，或在与组蛋白相互作用的行为中捕获的与Sin3相互作用的蛋白质的分子图像，试图使这些相互作用或缺乏这些相互作用如何导致疾病状态合理化，并为开发合适的分子疗法提供想法。

DESCRIPTION (provided by applicant): Regulation of eukaryotic gene expression at the transcriptional level relies on the coordinated action of multiple protein factors. The recruitment of multi-subunit coregulator complexes containing chromatin-modifying activities by sequence-specific DNA binding factors and chromatin-binding proteins to specific loci on the genome is an important step in regulating gene transcription. The Sin3 corepressor complex is one of only a handful of major corepressor complexes identified thus far in mammalian cells. The negative influence on gene transcription exerted by this complex relies in part on the action of nuclear histone deacetylases (HDACs), a group of enzymes that catalyze the hydrolysis of acetyl groups from acetylated chromatin substrates. The ~150 kDa Sin3 protein functions both as a molecular scaffold for corepressor complex assembly and interacts directly, or indirectly through other components of the complex, with a surprisingly large and diverse group of DNA-binding transcription factors and chromatin-binding proteins that play important roles in normal growth, development, and cellular homeostasis. Our studies for the next funding period will address questions broadly relating to how components of the Sin3 corepressor complex are recruited by diverse promoter-bound transcription factors on the one hand and by specific patterns of post-translationally modified histones, also referred to as "chromatin marks," on the other. Another major question relates to how the complex is assembled and how it contributes to its functional diversity. Answers to these questions rely on structure-function analyses. The primary tool for the structural investigations will be solution-state NMR spectroscopy because it is ideally suited for studies of transcription factors as they frequently harbor natively unfolded segments and also because of the relatively small size and tractable nature of the systems being studied. In addition, the technique is well-suited for studies of weak interactions such as those involving chromatin-binding modules. Functional analyses will rely on a variety of biochemical and biophysical approaches. The aims of the project broadly focus on three themes: (1) recruitment of the Sin3 corepressor by promoter-bound transcription factors, (2) recruitment and targeting of the corepressor complex to specific chromatin marks and (3) assembly of the core corepressor complex. PUBLIC HEALTH RELEVANCE: The transcription of eukaryotic genes into messenger RNAs for subsequent translation to produce proteins is regulated by a class of proteins known as transcriptional coregulators. These coregulators are recruited to specific regions of the genome by proteins that bind DNA specifically and/or by proteins that bind histones. The molecular interactions involving the Sin3 coregulator and those involving histone-binding proteins that interact with Sin3 are the focus of this proposal because little is known about how these proteins function and because defects in and abnormal amounts of these proteins are associated with diseases such as cancer. The proposed work will attempt to derive detailed molecular pictures of proteins captured in the act of interacting with Sin3 or those of Sin3-interacting proteins captured in the act of interacting with histones, attempt to rationalize how these interactions or lack thereof could lead to diseased states, and provide ideas for developing suitable molecular therapies.