Mechanism of transcript elongation control by RfaH

RfaH控制转录本延伸的机制

• 批准号: 8231348
• 负责人: IRINA ARTSIMOVITCH
• 金额: $ 36.61万
• 依托单位: OHIO STATE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2003
• 资助国家: 美国
• 起止时间: 2003-02-01 至 2014-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8231348
• 关键词: Address; Affect; Animal Model; Antibiotics; Attenuated; Bacteria; Bacterial Proteins; Bacteriophages; Binding; Binding Sites; Biochemical; Biochemical Genetics; Biological Assay; Bypass; C-terminal; Catalysis; Cell Wall; Cells; ChIP-on-chip; Chromatin; Complex; DNA; DNA Sequence; DNA lesion; DNA-Binding Proteins; DNA-Directed RNA Polymerase; Data; Dissection; Elongation Factor; Enzymes; Escherichia coli; Escherichia coli K12; Evolution; Family; Fertility; Fluorescence; Gene Expression; Gene Expression Profile; Gene Proteins; Genes; Genetic; Genetic Transcription; Genetic Translation; Goals; Grant; Human; Human Genome; In Vitro; Indium; Insecta; Kinetics; Klebsiella pneumonia bacterium; Life; Measurement; Mediating; Microarray Analysis; Modification; Molecular; Molecular Biology Techniques; Molecular Conformation; Molecular Models; Movement; Mutation; N-terminal; Nucleic Acids; Nucleotides; Operon; Orthologous Gene; Pectobacterium chrysanthemi; Plants; Precipitation; Property; Protein Family; Proteins; RNA; Recruitment Activity; Regulon; Research; Resources; Ribosomes; Roentgen Rays; Role; Salmonella enterica; Serratia; Side; Signal Transduction; Site; Specificity; Structure; Testing; Time; Transcript; Transcription Elongation; Transcriptional Regulation; Translations; Vibrio cholerae; Virulence; Virulence Factors; Work; Yersinia pestis; base; cell capsule; crosslink; density; design; genetic regulatory protein; in vitro activity; in vivo; molecular modeling; mutant; novel; paralogous gene; pathogen; prevent; public health relevance; research study; success; transcription factor; yeast two hybrid system

DESCRIPTION (provided by applicant): Elongation is the longest part of transcription cycle during which RNA polymerase movement along the template is hindered by many roadblocks DNA-bound proteins, DNA lesions, termination signals, etc. Factors that allow RNA polymerase to bypass these barriers are required for efficient synthesis of long RNAs in all domains of life. Bacterial protein RfaH regulates expression of the cell wall and capsule components, antibiotics, and virulence factors by increasing the RNA polymerase processivity. RfaH action depends on a DNA sequence called ops that mediates RfaH recruitment to RNA polymerase during elongation. In the first granting period, we obtained the X-ray structure of RfaH, identified its binding site on transcription complex, characterized RfaH effects at different regulatory sites and on enzymes with altered elongation properties, and showed that RfaH acts by preventing pausing rather than by increasing the rate of nucleotide addition. This mechanism is likely fundamentally conserved in other antiterminators. In this proposal, we will use a combination of biochemical, genetic, and structural approaches to address several aspects of RfaH action. The first goal of this project is to study the mechanism of RfaH action. We will use a combination of genetic, biochemical, and structural analyses to dissect interactions of the N-terminal domain (which is sufficient for RfaH anti-pausing activity) with the transcription elongation complex and to elucidate the confomational changes triggered by these interactions. The second goal of this project is to elucidate the role of the ops element in recruitment of RfaH. We propose that ops not only establishes base-specific contacts with RfaH but also induces a specialized scrunched DNA conformation that is required for RfaH binding. The third goal of this project is to test if the "modulatory" C-terminal domain changes its structure after RfaH recruitment and is involved in cross-talk with the translation apparatus. The fourth goal of this project is to characterize the RfaH regulon by identifying the RfaH-associated proteins and genes by in vivo crosslinking and chromatin immuno-precipitation, respectively. We will also analyze selected RfaH operons by quantitative RT PCR. PUBLIC HEALTH RELEVANCE: This project aims to elucidate the mechanism by which transcription factor RfaH regulates gene expression. The rfaH genes are present in human, insect, and plant pathogens; moreover, RfaH is essential for virulence in animal models. These studies will reveal the mechanism of RfaH action, elucidate the unique role of its DNA target site in transcriptional control, and identify cellular RfaH targets which may be uncharacterized virulence factors.

描述（由申请人提供）：延伸是转录周期中最长的部分，在此期间RNA聚合酶沿模板沿着移动受到许多路障DNA结合蛋白、DNA损伤、终止信号等的阻碍。允许RNA聚合酶绕过这些障碍的因子是在所有生命领域中有效合成长RNA所必需的。细菌蛋白RfaH通过增加RNA聚合酶的持续合成能力来调节细胞壁和荚膜成分、抗生素和毒力因子的表达。RfaH的作用依赖于一个称为ops的DNA序列，该序列在延伸过程中介导RfaH向RNA聚合酶的募集。在第一个授权期间，我们获得了RfaH的X射线结构，确定了其在转录复合物上的结合位点，表征了RfaH在不同调控位点和具有改变的延伸特性的酶上的作用，并表明RfaH通过防止暂停而不是通过增加核苷酸添加的速率来起作用。这种机制可能在其他抗终止剂中基本上是保守的。在这项提案中，我们将使用生物化学，遗传学和结构方法的组合来解决RfaH行动的几个方面。本项目的第一个目标是研究RfaH的作用机制。我们将使用遗传，生物化学和结构分析的组合，解剖的N-末端结构域（这是足够的RfaH抗暂停活性）与转录延伸复合物的相互作用，并阐明这些相互作用引发的构象变化。本项目的第二个目标是阐明项目事务处在招募人道主义援助人员方面的作用。我们建议，OPS不仅建立了与RfaH的碱基特异性接触，而且还诱导了RfaH结合所需的专门的scrunched DNA构象。该项目的第三个目标是测试“调节性”C-末端结构域在RfaH募集后是否改变其结构，并参与与翻译装置的串扰。本项目的第四个目标是通过分别在体内交联和染色质免疫沉淀鉴定RfaH相关蛋白和基因来表征RfaH调节子。我们还将通过定量RT PCR分析选定的RfaH操纵子。 公共卫生相关性：该项目旨在阐明转录因子RfaH调节基因表达的机制。rfaH基因存在于人类、昆虫和植物病原体中;此外，RfaH对于动物模型中的毒力是必需的。这些研究将揭示RfaH的作用机制，阐明其DNA靶位点在转录调控中的独特作用，并确定可能是未知毒力因子的细胞RfaH靶点。