Regulation of DNA Damage Induced Genes by Yeast TAFIIs
酵母TAFII对DNA损伤诱导基因的调控
基本信息
- 批准号:7882088
- 负责人:
- 金额:$ 28.47万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2009
- 资助国家:美国
- 起止时间:2009-08-03 至 2011-07-31
- 项目状态:已结题
- 来源:
- 关键词:BiochemicalBirthCandidate Disease GeneCell NucleusCellsComplementComplexCytoplasmDNA DamageDNA Microarray ChipDNA SequenceDataDiseaseElongation FactorEventGene ExpressionGene Expression RegulationGeneral Transcription FactorsGenesGeneticGenetic TranscriptionGenomeGenomicsGoalsHealthHumanKnowledgeLeftLinkMediatingMediator of activation proteinMessenger RNAModelingMolecularMolecular GeneticsNaturePlayPost-Transcriptional RegulationProcessProteinsPublishingRecruitment ActivityRegulationRoleSAGASaccharomycetalesSequence-Specific DNA Binding ProteinSiteSpecific qualifier valueStagingSyndromeSystemTestingTranscription ProcessTransport ProcessWorkYeastsbasechromatin remodelingfascinategenetic analysishuman diseaseinsightnoveltranscription factor
项目摘要
DESCRIPTION (provided by applicant): The regulation of gene expression is a fundamental process in cells, and alterations in this process have been linked to numerous disease states in humans. It is regulated at multiple levels, requiring highly coordinated and integrated events including chromatin remodeling, initiation, elongation, processing and ultimately the destruction of mRNA. Determining how these events are coordinated is central to understanding gene expression. The overall objective of this proposal is to understand how transcription factor complexes coordinate multiple steps in gene regulation. This proposal will examine the functions of the Ccr4-Not complex, exploiting the powerful genetic system of yeast. The Ccr4-Not complex has many ties to the general transcription factor complex TFIID, particularly the TAFII subunits. Genetic, biochemical and molecular approaches are proposed. Aim 1 will characterize the functions of the Ccr4- Not transcription complex in the process of transcription. This complex displays multiple physical and genetic links to TFIID, the general transcription machinery and elongation factors. Its role in multiple stages in the transcription cycle will be examined using RNR3 as a model gene. Aim 2 will identify the targeting mechanism for Ccr4-Not. It regulates a subset of genes, and appears not be universally required for all transcription in the cell. We will explore the DNA sequence and transcription factor requirements for its recruitment and function at RNR3. Aim 3 will employ genomics based approaches to identify novel Ccr4-Not dependent genes and identify the features of the genome that specifies regulation by this complex. The intersection of these approaches will allow for a greater understanding of the coordination of multiple steps in transcription. The completion of these aims will: (1) uncover how multiple steps in gene expression are coordinated and regulated; (2) define the functions of a highly conserved eukaryotic transcription factor complex implicated in human disease; (3) lay the groundwork for identifying how specific mRNAs are marked for post-transcriptional control.
Project Narrative - Relevance: Cells require precise control over the expression of their genes, and numerous human diseases and syndromes are caused by disturbances in gene expression. A multitude of transcription factors coordinate their activities to regulate this important process. The goal of the work described here is to understand how transcription factors control the level of gene expression; thus, completion of this work is directly relevant to human health.
描述(由申请人提供):基因表达的调节是细胞中的基本过程,并且该过程中的改变与人类的许多疾病状态有关。它在多个水平上受到调节,需要高度协调和整合的事件,包括染色质重塑,起始,延伸,加工和最终破坏mRNA。确定这些事件是如何协调的是理解基因表达的核心。本提案的总体目标是了解转录因子复合物如何协调基因调控中的多个步骤。该提案将研究Ccr 4-Not复合物的功能,利用酵母强大的遗传系统。Ccr 4-Not复合物与一般转录因子复合物TFIID,特别是TAFII亚基有许多联系。提出了遗传学、生物化学和分子生物学方法。目的1研究Ccr 4- Not转录复合体在转录过程中的功能。该复合物显示与TFIID、一般转录机制和延伸因子的多种物理和遗传联系。它在转录周期的多个阶段中的作用将使用RNR 3作为模型基因进行检查。目的2将确定Ccr 4-Not的靶向机制。它调节基因的一个子集,并且似乎不是细胞中所有转录普遍需要的。我们将探讨其在RNR 3的招募和功能的DNA序列和转录因子的要求。目标3将采用基于基因组学的方法来鉴定新的Ccr 4-Not依赖基因,并鉴定指定由该复合物调节的基因组特征。这些方法的交叉将允许更好地理解转录中多个步骤的协调。这些目标的完成将:(1)揭示基因表达中的多个步骤是如何协调和调节的;(2)定义与人类疾病有关的高度保守的真核转录因子复合体的功能;(3)为识别特定mRNA如何标记用于转录后控制奠定基础。
项目叙述-相关性:细胞需要精确控制其基因的表达,并且许多人类疾病和综合征是由基因表达的干扰引起的。许多转录因子协调它们的活动来调节这一重要过程。本文所述工作的目标是了解转录因子如何控制基因表达水平;因此,这项工作的完成与人类健康直接相关。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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JOSEPH C REESE其他文献
JOSEPH C REESE的其他文献
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{{ truncateString('JOSEPH C REESE', 18)}}的其他基金
Activities of yeast Ccr4-Not transcription factor complex - Supplement
酵母 Ccr4-Not 转录因子复合物的活性 - 补充剂
- 批准号:
10797863 - 财政年份:2020
- 资助金额:
$ 28.47万 - 项目类别:
Activities of yeast Ccr4-Not transcription factor complex
酵母Ccr4-Not转录因子复合物的活性
- 批准号:
10596993 - 财政年份:2020
- 资助金额:
$ 28.47万 - 项目类别:
Activities of yeast Ccr4-Not transcription factor complex
酵母Ccr4-Not转录因子复合物的活性
- 批准号:
10364658 - 财政年份:2020
- 资助金额:
$ 28.47万 - 项目类别:
Eukaryotic Gene Regulation (EGR) Predoctoral Training Program
真核基因调控(EGR)博士前培训项目
- 批准号:
10451768 - 财政年份:2018
- 资助金额:
$ 28.47万 - 项目类别:
Eukaryotic Gene Regulation (EGR) Predoctoral Training Program
真核基因调控(EGR)博士前培训项目
- 批准号:
10179424 - 财政年份:2018
- 资助金额:
$ 28.47万 - 项目类别:
Regulation of DNA Damage Induced Genes by Yeast TAFIIs
酵母TAFII对DNA损伤诱导基因的调控
- 批准号:
8847902 - 财政年份:2014
- 资助金额:
$ 28.47万 - 项目类别:
REGULATION OF DNA DAMAGE INDUCED GENES BY YEAST TAFIIS
酵母 TAFIIS 对 DNA 损伤诱导基因的调控
- 批准号:
6343048 - 财政年份:1999
- 资助金额:
$ 28.47万 - 项目类别:
Regulation of DNA Damage Induced Genes by Yeast TAFIIs
酵母TAFII对DNA损伤诱导基因的调控
- 批准号:
6825873 - 财政年份:1999
- 资助金额:
$ 28.47万 - 项目类别:
Regulation of DNA Damage Induced Genes by Yeast TAFIIs
酵母TAFII对DNA损伤诱导基因的调控
- 批准号:
7741694 - 财政年份:1999
- 资助金额:
$ 28.47万 - 项目类别:
REGULATION OF DNA DAMAGE INDUCED GENES BY YEAST TAFIIS
酵母 TAFIIS 对 DNA 损伤诱导基因的调控
- 批准号:
6418015 - 财政年份:1999
- 资助金额:
$ 28.47万 - 项目类别:
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