Conformational Dynamics of E. coli CytR Protein in Regulation of Gene Expression

大肠杆菌 CytR 蛋白在基因表达调控中的构象动力学

• 批准号: 0719373
• 负责人: Donald Senear
• 金额: $ 57.01万
• 依托单位: University of California-Irvine
• 依托单位国家: 美国
• 项目类别: Standard Grant
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-08-01 至 2011-07-31
• 项目状态: 已结题
• 来源: https://www.nsf.gov/awardsearch/showAward?AWD_ID=0719373&HistoricalAwards=false
• 关键词: Conformational; Dynamics; E.; coli; CytR

The need for the temporal control of gene expression during development, differentiation or metabolic regulation is fundamental to biology. A primary mechanism for controlling expression of individual genes occurs at the level of initiation of transcription and employs regulatory proteins (transcriptional activators or repressors) that bind to specific DNA control sequences (or operators). These operators are located near the sites where RNA polymerase binds and initiates transcription (promoters); the DNA-protein complexes modulate the efficiency of formation of transcription initiation complexes and thereby control the level of gene expression. Multiple transcriptional regulators are typically involved in regulating the transcription of a particular gene. The level of expression depends on external signals or effectors, and the arrangement of the operators and their associated regulatory proteins on the DNA. Some of the regulatory proteins can act at many different promoters whereas others are promoter specific. These combinatorial mechanisms generate great diversity and can provide over time, coordinate control of many genes as well as fine-tuning of the expression of individual genes. This project addresses the combinatorial control mechanism in a gene family known as the CytR regulon in the bacterium Escherichia coli. Two regulatory proteins working in concert produce both coordinate and differential regulation patterns in seven unlinked genes. The regulatory proteins involved are the global gene regulator CRP and a CytR-specific protein. The interplay between these two proteins and the different arrangements of the respective operator elements at the seven gene promoters of the Cyt regulon underlies this complex combinatorial regulation. This project will employ a multi-disciplinary approach (i) to determine the structures and dynamics of the regulatory proteins and their complexes with DNA, (ii) to probe the effects of interactions between the proteins when bound to DNA and (iii) to develop quantitative understanding of the kinetic mechanisms of transcriptional activation mediated by the specific promoter sequence and the specific protein-protein interactions at that promoter. This will generate a comprehensive view of the molecular mechanisms of combinatorial gene regulation at the structure/function level. Developing this molecular understanding of gene regulation in this bacterial system will have broad impacts on our understanding of not only bacterial physiology, but also on the genetic control of differentiation and development in eukaryotic organisms. The project will also provide multi-disciplinary training for postdoctoral, predoctoral and undergraduate level scientists in structural biology, molecular biophysics, and molecular genetics.

在发育、分化或代谢调节过程中对基因表达的时间控制的需要是生物学的基础。控制单个基因表达的主要机制发生在转录起始水平，并采用与特定 DNA 控制序列（或操纵子）结合的调节蛋白（转录激活子或阻遏子）。这些操纵子位于 RNA 聚合酶结合并启动转录的位点附近（启动子）； DNA-蛋白质复合物调节转录起始复合物的形成效率，从而控制基因表达水平。多个转录调节因子通常参与调节特定基因的转录。表达水平取决于外部信号或效应器，以及操纵子及其相关调节蛋白在 DNA 上的排列。 一些调节蛋白可以作用于许多不同的启动子，而另一些则具有启动子特异性。这些组合机制产生巨大的多样性，并且可以随着时间的推移提供对许多基因的协调控制以及单个基因表达的微调。该项目致力于解决大肠杆菌 CytR 调节子基因家族的组合控制机制。两个调节蛋白协同工作，在七个不相关的基因中产生协调和差异调节模式。涉及的调节蛋白是全局基因调节蛋白 CRP 和 CytR 特异性蛋白。这两种蛋白质之间的相互作用以及 Cyt 调节子的七个基因启动子处各自操纵子元件的不同排列构成了这种复杂的组合调节的基础。该项目将采用多学科方法（i）确定调节蛋白及其与 DNA 的复合物的结构和动力学，（ii）探索与 DNA 结合时蛋白质之间相互作用的影响，以及（iii）开发定量了解由特定启动子序列介导的转录激活动力学机制以及该启动子处的特定蛋白质-蛋白质相互作用。这将在结构/功能水平上产生组合基因调控分子机制的全面视图。发展这种细菌系统中基因调控的分子理解不仅将对我们对细菌生理学的理解产生广泛的影响，而且对真核生物分化和发育的遗传控制的理解也将产生广泛的影响。该项目还将为结构生物学、分子生物物理学和分子遗传学领域的博士后、博士前和本科生科学家提供多学科培训。