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Gene Regulatory Codes and Signal/Regulatory Element Interactions in IME2

Gene Regulatory Codes and Signal/Regulatory Element Interactions in IME2
IME2 中的基因调控代码和信号/调控元件相互作用
批准号:
7254454
负责人:
SAUL M HONIGBERG
金额:
$22.35万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-03-01 至 2010-02-28

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中文摘要
翻译
描述(由申请人提供):Honigberg实验室的长期目标是确定酵母调节其向减数分裂途径过渡的机制。该系统提供了一个独特的机会来研究不同信号被整合以控制细胞命运的基本机制。该提议的第一个具体目的是确定IME 2的基因调控密码,即鉴定控制该基因表达的所有调控元件以及它们响应的一个或多个信号。这一目的将通过基因组ime 2-lacZ等位基因的启动子的广泛诱变,然后在调节该基因的三个主要信号的所有组合下测定每个ime 2-x-lacZ突变体来实现。对这种序列和表达数据的组合的分析将揭示基因调控密码的逻辑电路。该提案的第二个目的是确定IME 2监管要素之间的相互作用。该目的的第一部分将通过测量所选ime 2-x-lacZ等位基因对Ime 1 p和Rpd 3 p与IME 2的URS 1调节元件的关联的影响来实现。该目标的第二部分将是确定具有共享功能的IME 2调节元件之间的相互作用。这将通过上位性(双突变体分析)完成。由于拟议的研究将导致真核基因调控密码的第一个完整描述,完成这个项目提供了一个框架,了解其他基因的调控密码,包括基因的表达改变导致人类疾病。转录调控的缺陷对人类健康有着深远的影响,影响着糖尿病、癌症和帕金森氏症等多种疾病。由于转录调控的机制是复杂的,仍然知之甚少,研究转录调控的模式遗传生物,芽殖酵母S。酿酒酵母,可以导致基本的发现,推进我们对这些疾病的病因学的理解。
英文摘要
DESCRIPTION (provided by applicant): The long-term objective of the Honigberg lab is to identify the mechanisms by which yeast regulate their transition into the meiotic pathway. This system presents a unique opportunity to study fundamental mechanisms by which diverse signals are integrated to control cellular fates. The first specific aim of the proposal is to determine the gene regulatory code for IME2, i.e. to identify all of the regulatory elements that control expression of this gene and the signal or signals to which they respond. This aim will be achieved through extensive mutagenesis of the promoter of a genomic ime2-lacZ allele, followed by assaying each ime2-x-lacZ mutant under all combinations of the three major signals that regulate this gene. Analysis of this combination of sequence and expression data will reveal the logic circuits underlying the gene regulatory code. The second aim of the proposal is to identify interactions between IME2 regulatory elements. The first part of this aim will be accomplished by measuring the effect of selected ime2-x-lacZ alleles on association of Ime1p and Rpd3p with the URS1 regulatory element of IME2. The second part of this aim will be to determine the interactions between IME2 regulatory elements that have shared functions. This will be accomplished by epistasis (double mutant analysis). Because the proposed research will result in the first complete description of a eukaryotic gene regulatory code, accomplishing this project provides a framework for understanding regulatory codes in other genes, including genes whose altered expression results in human disease. Defects in the regulation of transcription have profound effects on human health, affecting such diverse diseases as diabetes, cancer, and Parkinson's. Because the mechanism of transcriptional regulation is complex and still poorly understood, studying transcriptional regulation in a model genetic organism, the budding yeast S. cerevisiae, can lead to fundamental discoveries that advance our understanding of the etiology of these diseases.
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