Mechanisms of DNA binding and gene regulation by C2H2 zinc finger proteins

C2H2 锌指蛋白的 DNA 结合和基因调控机制

• 批准号: RGPIN-2018-05962
• 负责人: ShateriNajafabadi, Hamed
• 金额: $ 2.99万
• 依托单位: McGill University
• 依托单位国家: 加拿大
• 项目类别: Discovery Grants Program - Individual
• 财政年份: 2019
• 资助国家: 加拿大
• 起止时间: 2019-01-01 至 2020-12-31
• 项目状态: 已结题
• 来源: https://www.nserc-crsng.gc.ca/ase-oro/Details-Detailles_eng.asp?id=688301
• 关键词: Mechanisms; DNA; binding; gene; regulation

The genome encodes highly detailed instructions indicating when and where different genes need to be active in the cell. A massively complex network of proteins called “transcription factors” executes these regulatory instructions. Transcription factors regulate the activity of genes by binding to very specific sites on the genome. This remarkable specificity is mediated by their ability to recognize particular “DNA sequences”, words that are made of the DNA alphabet and mark the genomic sites that should be bound by each transcription factor.******With over 700 members, the “C2H2” zinc finger family constitutes the largest class of regulatory proteins. My previous research has shown that the C2H2 proteins recognize the most diverse set of DNA sequences among transcription factors, regulate the activation of a large number of genes, affect various cellular pathways, and have been a driving force in the evolution of the mammalian genome. However, the molecular mechanisms that underlie this functional diversity have only been partially characterized. Our research aims to understand the principles of DNA binding and gene regulation by C2H2 proteins.******Here, we aim to study the molecular mechanisms that allow the C2H2 proteins to recognize diverse DNA sequences. We focus on two aspects of this diversity: (a) the ability of C2H2 proteins to recognize multiple distinct DNA sequences through utilization of different parts of the protein, and (b) their ability to read “epigenetic” marks, a second layer of information that the cell overlays on top of the genetic information in order to precisely control the architecture and the activity of the genome. We will develop novel computational models that connect the structure of C2H2 proteins to the genetic and epigenetic alphabet that they recognize, revealing how regulatory instructions are read and interpreted by these proteins at the molecular level. These models will help us better understand the mechanisms of gene regulation by C2H2 proteins, trace their evolutionary origins, and reveal new functions for them. They will also enable us to predict the molecular functions of previously uncharacterized C2H2 proteins. Given the central role of these proteins in the evolution and function of our genome, these studies will allow us to decipher the fundamental principles that govern our biology.**

基因组编码高度详细的指令，指示不同基因在细胞中何时何地需要活跃。一个被称为“转录因子”的蛋白质的巨大复杂网络执行这些调控指令。转录因子通过与基因组上非常特异的位点结合来调节基因的活性。这种显著的特异性是由它们识别特定“DNA序列”的能力介导的，DNA序列是由DNA字母组成的单词，并标记应该被每个转录因子结合的基因组位点。C2H2锌指蛋白家族有700多个成员，是最大的一类调控蛋白。我以前的研究表明，C2H2蛋白识别转录因子中最多样化的DNA序列，调节大量基因的激活，影响各种细胞途径，并一直是哺乳动物基因组进化的驱动力。然而，这种功能多样性背后的分子机制仅得到部分表征。我们的研究旨在了解C2H2蛋白的DNA结合和基因调控的原理。在这里，我们的目标是研究的分子机制，使C2H2蛋白识别不同的DNA序列。 我们关注这种多样性的两个方面：（a）C2H2蛋白通过利用蛋白质的不同部分识别多个不同DNA序列的能力，以及（B）它们读取“表观遗传”标记的能力，表观遗传标记是细胞覆盖在遗传信息之上的第二层信息，以精确控制基因组的结构和活性。我们将开发新的计算模型，将C2H2蛋白质的结构与它们识别的遗传和表观遗传字母表连接起来，揭示这些蛋白质在分子水平上如何阅读和解释调控指令。这些模型将帮助我们更好地了解C2H2蛋白的基因调控机制，追踪它们的进化起源，并揭示它们的新功能。它们还将使我们能够预测以前未表征的C2H2蛋白的分子功能。 鉴于这些蛋白质在我们基因组的进化和功能中的核心作用，这些研究将使我们能够破译支配我们生物学的基本原则。