Role of Set2 and H3 methylation in chromatin function

描述（由申请人提供）：组蛋白甲基化在染色质组织和基因转录调控中起着重要作用。我们的长期目标是阐明赖氨酸特异性组蛋白甲基转移酶如何调节基因表达并促进细胞发育和疾病。其中一种在真核生物中高度保守的酶是组蛋白H3赖氨酸36 （H3K36）甲基转移酶Set2。我们和其他人已经证明，在转录延伸过程中，Set2与RNA聚合酶II相关，并且它在H3K36位点的甲基化指导组蛋白去乙酰化酶复合物（Rpd3S）的募集，从而抑制转录的不适当起始。虽然Set2的基本功能已经被表征，但关于Set2酶本身是如何被调节的，ii)该酶是否存在其他功能，以及iii) H3K36的不同甲基化状态（me1， me2和me3）及其去甲基化如何有助于染色质组织和基因转录，仍然知之甚少。我们计划以酿酒酵母为模型生物，结合生物化学和遗传学进一步研究Set2和H3K36me在转录调控等方面的功能。我们的目标是解决一些广泛的问题，这些问题将促进我们对组蛋白甲基转移酶和去甲基化酶如何调节染色质环境和促进基因表达的理解。这些问题包括：1)Set2是如何靶向基因的，又是如何通过翻译后修饰进行调控的？2) H3K36去甲基化如何参与转录过程？3)不同的H3K36甲基化状态是否在转录中具有不同的生物活性，该组蛋白“标记”是否在其他DNA相关活动中起作用，如DNA修复和复制？这些研究将对该领域产生重大影响，因为我们目前对组蛋白翻译后修饰，特别是H3K36甲基化的了解非常有限。介导H3K36甲基化的酶的失调导致包括癌症在内的多种人类疾病，这一事实强调了这一点。考虑到哺乳动物细胞中具有多种h3k36甲基化酶的复杂性，酵母提供了应用遗传学和生物化学来理解染色质中高度重要的组蛋白“标记”的基本功能的卓越能力。

DESCRIPTION (provided by applicant): Histone methylation plays a fundamental role in the organization of chromatin and in the regulation of gene transcription. Our long-term goal is to elucidate how lysine-specific histone methyltransferases regulate gene expression and contribute to cellular development and disease. One such enzyme that is highly conserved in eukaryotes is the histone H3 lysine 36 (H3K36) methyltransferase Set2. We, and others, have shown that Set2 associates with RNA polymerase II during transcription elongation, and that its methylation at H3K36 directs the recruitment of a histone deacetylase complex (Rpd3S) that suppresses inappropriate initiation of transcription. While the basic functions of Set2 have been characterized, little is still known regarding: i) how the Set2 enzyme itself is regulated, ii) whether other functions for this enzyme exist, and iii) how the distinct methylation states of H3K36 (me1, me2, and me3) and their demethylation contribute to chromatin organization and gene transcription. Using Saccharomyces cerevisiae as a model organism, we plan to use a combination of biochemistry and genetics to further address the functions of Set2 and H3K36me in transcriptional regulation and beyond. Our goal will be to address a number of broad questions that will advance our understanding of how histone methyltransferases and demethylases regulate the chromatin environment and contribute to gene expression. These include: 1) How is Set2 targeted to genes and is itself regulated by post- translational modification? 2) How does H3K36 demethylation contribute to the transcription process? 3) Do the different H3K36 methylation states have distinct biological activities in transcription, and does this histone 'mark' function in other DNA- related activities such as DNA repair and replication? These studies will have a significant impact to the field, as our current understanding of histone post-translational modifications, including H3K36 methylation in particular, is very limited. This is underscored by the fact that the dysregulation of enzymes that mediate H3K36 methylation lead to a variety of human diseases including cancer. Given the complexity of having multiple H3K36-methylating enzymes in mammalian cells, yeast affords the exceptional ability to apply genetics and biochemistry to understand the fundamental functions of a highly significant histone 'mark' in chromatin.