DEVELOPMENT OF CELL POLARITY IN BUDDING YEAST
DEVELOPMENT OF CELL POLARITY IN BUDDING YEAST
批准号:
6490070
负责人:
DAVID G DRUBIN
金额:
$33.55万
依托单位国家:
美国
项目类别:
财政年份:
1997
资助国家:
美国
项目状态:
已结题
起止时间:
1997-01-01 至 2004-12-31
关键词:
Saccharomyces cerevisiae actins biological polymorphism biological signal transduction cell cycle proteins cell growth regulation cellular polarity cytoskeletal proteins endocytosis fungal genetics gene mutation guanine nucleotide binding protein guanosinetriphosphatases laboratory rabbit microorganism growth microorganism reproduction molecular genetics protein kinase protein protein interaction protein structure function yeast two hybrid system
中文摘要
描述(来自申请人摘要的逐字记录):S。酿酒厂是一个
由于其强大的生物学特性,
遗传学,它的简单性,观察极性发展的能力
在细胞群体中同步,以及存在许多突变和
细胞极性的分子标记研究将确定Cdc 42 GT3是如何
控制肌动蛋白组织,以及肌动蛋白如何介导极化内吞作用。
37个定点cdc 42突变体将在
透化的酵母和肌动蛋白组装能力的酵母提取物,
生物化学活性到体内功能,并用于遗传筛选,
识别下游途径的组成部分。Cdc 42效应器Pak的作用
激酶在形态发生中的作用将通过遗传和化学遗传学方法阐明,
战略布局在假菌丝生长中有缺陷的特殊cdc 42等位基因将是
研究,以提供更深入的了解真菌的分子基础,
二型性,这是许多真菌病原体的特征。最后,一个复杂的
一组相互作用的蛋白质将内吞膜连接到Arp 2/3复合物,
以及这些蛋白质是如何被本研究中发现的新型方舟激酶调节的。
实验室将进行调查。
英文摘要
DESCRIPTION (Verbatim from the applicant's abstract): S. cerevisiae is an
excellent organism for studies of cell polarity development due to its powerful
genetics, its simplicity, the ability to observe polarity development
synchronously in a cell population, and existence of numerous mutations and
molecular markers for cell polarity. Studies will determine how Cdc42 GTPase
controls actin organization, and how actin mediates polarized endocytosis.
Thirty-seven site-directed cdc42 mutants will be characterized biochemically in
permeabilized yeast and in actin-assembly competent yeast extracts to relate
biochemical activities to in vivo functions, and used in genetic screens to
identify components of downstream pathways. Roles for Cdc42 effector Pak
kinases in morphogenesis will be elucidated by genetic and chemical-genetic
strategies. Special cdc42 alleles defective in pseudohyphal growth will be
studied to provide a deeper understanding of the molecular basis for fungal
dimorphism, a characteristic of many fungal pathogens. Finally, how a complex
set of interacting proteins links endocytic membranes to the Arp2/3 complex,
and how these proteins are regulated by novel Ark kinases discovered in this
laboratory, will be investigated.
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会议论文
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批准号:8365818
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项目类别:
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资助金额:$1.28万
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财政年份:2011
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负责人:DAVID G DRUBIN
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依托单位:
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批准号:8362731
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项目类别:
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资助金额:$2.94万
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财政年份:2011
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负责人:DAVID G DRUBIN
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依托单位:
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批准号:8171310
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项目类别:
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资助金额:$0.24万
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财政年份:2010
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IDENTIFICATION OF NOVEL MEMBERS OF S CEREVISIAE CYTOKINESIS APPARATUS
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资助金额:$0.24万
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财政年份:2010
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PROTEIN COMPOSITION OF ACTIN TAILS ASSEMBLED IN YEAST EXTRACTS
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IDENTIFY PHOSPHORYLATION SITES AND POTENTIAL SUBSTRATES OF YPK1P
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财政年份:2010
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依托单位:
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财政年份:2009
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负责人:DAVID G DRUBIN
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依托单位:
PROTEIN COMPOSITION OF ACTIN TAILS ASSEMBLED IN YEAST EXTRACTS
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批准号:7957840
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项目类别:
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资助金额:$0.33万
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财政年份:2009
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负责人:DAVID G DRUBIN
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依托单位:
KINETOCHORE PROTEIN INTERACTIONS AND THEIR REGULATORY KINASES
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资助金额:$0.33万
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负责人:DAVID G DRUBIN
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依托单位:
GENERATING A PROTEIN INTERACTION MAP OF A VIRAL KILLER TOXIN
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财政年份:2008
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负责人:DAVID G DRUBIN
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依托单位:
海外基金