GENETIC ANALYSIS OF ENZYME PROCESSING AND LOCALIZATION
酶加工和定位的遗传分析
基本信息
- 批准号:6519047
- 负责人:
- 金额:$ 28.96万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1981
- 资助国家:美国
- 起止时间:1981-07-01 至 2004-03-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
The yeast vacuole resembles an animal cell lysosome, for it is an acidic
compartment, contains a complement of hydrolases, and is the final
destination of ligands taken up by fluid phase and receptor-mediated
endocytosis. Since yeast is amenable to genetical, biochemical and
molecular analysis and since fundamental biological processes have been
almost obsessively conserved across eukaryotes, yeast offers an excellent
model system for studies of the function and assembly of this important
organelle. These studies may contribute to our understanding of the
mannose-6-phosphate independent pathway of lysosomal/vacuolar enzyme
targeting and of membrane assembly. They may enable understanding of the
missorting of lysosomal proteases that occurs in some pathologic
conditions like breast cancer. The overall goals of this research are to
understand in molecular detail how proteins are targeted to the vacuole,
how the organelle is assembled, and how it functions as a digestive and
homeostatic organelle. Mutants unable to properly sort vacuolar hydrolases
(pep7 and pep12) or to acidify (vph1) or assemble (pep5) the vacuole were
isolated and the corresponding genes cloned. The specific aims in this
proposal are 1) to determine whether Pepl2p, which is required for lumenal
hydrolase targeting, is in both Golgi and vacuolar membranes, whether it
functions by cycling between the two organelles, whether this cycling is
essential for its function, what its function is, and what other proteins
it interacts with as it carries out its functions 2) to determine whether
Pep7p, which is required for lumenal hydrolase targeting, is in the
nucleus, whether it functions as a transcription factor, what genes it
regulates if it does and what the functions of the regulated genes are 3)
to determine whether VPH1 and STV1 encode organelle specific ATPase
subunits, what the organelles are, whether there are other members of the
gene family, and if so, clone and study them, and to determine the
topology of Vph1p in the vacuolar membrane 4) to determine the domain
structure of Pep5p, which is required for formation of vacuoles, to
identify other proteins with which it interacts in assembling the vacuole,
and determine whether loss of function of these proteins gives similar
phenotypes 5) to recover the gene(s) encoding the vacuolar Ca2+
transporter, make mutations, and use them to probe the role of the
transporter and organelle in cellular Ca2+ homeostasis. Methods will
include targeted mutagenesis, suppressor selection and analysis,
subcellular fractionation, biochemistry, and immunofluorescence.
酵母液泡类似于动物细胞溶酶体,因为它是酸性的
项目成果
期刊论文数量(12)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Genetic instability of clathrin-deficient strains of Saccharomyces cerevisiae.
网格蛋白缺陷型酿酒酵母菌株的遗传不稳定性。
- DOI:10.1093/genetics/124.1.27
- 发表时间:1990
- 期刊:
- 影响因子:3.3
- 作者:Lemmon,SK;Freund,C;Conley,K;Jones,EW
- 通讯作者:Jones,EW
Pep3p/Pep5p complex: a putative docking factor at multiple steps of vesicular transport to the vacuole of Saccharomyces cerevisiae.
Pep3p/Pep5p 复合物:囊泡运输到酿酒酵母液泡的多个步骤中的假定对接因子。
- DOI:10.1093/genetics/156.1.105
- 发表时间:2000
- 期刊:
- 影响因子:3.3
- 作者:Srivastava,A;Woolford,CA;Jones,EW
- 通讯作者:Jones,EW
Protease B of Saccharomyces cerevisiae: isolation and regulation of the PRB1 structural gene.
- DOI:10.1093/genetics/115.2.255
- 发表时间:1987-02
- 期刊:
- 影响因子:3.3
- 作者:C. Moehle;M. W. Aynardi;M. Kolodny;F. J. Park;E. W. Jones
- 通讯作者:C. Moehle;M. W. Aynardi;M. Kolodny;F. J. Park;E. W. Jones
The Sec1/Munc18 protein, Vps33p, functions at the endosome and the vacuole of Saccharomyces cerevisiae.
Sec1/Munc18 蛋白 Vps33p 在酿酒酵母的内体和液泡中发挥作用。
- DOI:10.1091/mbc.e03-10-0767
- 发表时间:2004
- 期刊:
- 影响因子:3.3
- 作者:Subramanian,Shoba;Woolford,CarolA;Jones,ElizabethW
- 通讯作者:Jones,ElizabethW
Genetic interactions between a pep7 mutation and the PEP12 and VPS45 genes: evidence for a novel SNARE component in transport between the Saccharomyces cerevisiae Golgi complex and endosome.
pep7 突变与 PEP12 和 VPS45 基因之间的遗传相互作用:酿酒酵母高尔基体复合体和内体之间运输中新的 SNARE 成分的证据。
- DOI:10.1093/genetics/147.2.467
- 发表时间:1997
- 期刊:
- 影响因子:3.3
- 作者:Webb,GC;Hoedt,M;Poole,LJ;Jones,EW
- 通讯作者:Jones,EW
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ELIZABETH W JONES其他文献
ELIZABETH W JONES的其他文献
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{{ truncateString('ELIZABETH W JONES', 18)}}的其他基金
SEARCH FOR RESIDENT ER PROTEINS THAT INTERACT WITH PBN1P.
搜索与 PBN1P 相互作用的驻留 ER 蛋白质。
- 批准号:
6979635 - 财政年份:2004
- 资助金额:
$ 28.96万 - 项目类别:
PBN1P AND RESIDENT ENDOPLASMIC RETICULUM PROTEINS
PBN1P 和驻留内质网蛋白
- 批准号:
6979634 - 财政年份:2004
- 资助金额:
$ 28.96万 - 项目类别:
GENETIC ANALYSIS OF ENZYME PROCESSING AND LOCALIZATION
酶加工和定位的遗传分析
- 批准号:
2853596 - 财政年份:1981
- 资助金额:
$ 28.96万 - 项目类别:
GENETIC ANALYSIS OF ENZYME PROCESSING AND LOCALIZATION
酶加工和定位的遗传分析
- 批准号:
3277341 - 财政年份:1981
- 资助金额:
$ 28.96万 - 项目类别:
GENETIC ANALYSIS OF ENZYME PROCESSING AND LOCALIZATION
酶加工和定位的遗传分析
- 批准号:
3277346 - 财政年份:1981
- 资助金额:
$ 28.96万 - 项目类别:
GENETIC ANALYSIS OF ENZYME PROCESSING AND LOCALIZATION
酶加工和定位的遗传分析
- 批准号:
3277343 - 财政年份:1981
- 资助金额:
$ 28.96万 - 项目类别:
GENETIC ANALYSIS OF ENZYME PROCESSING AND LOCALIZATION
酶加工和定位的遗传分析
- 批准号:
3277345 - 财政年份:1981
- 资助金额:
$ 28.96万 - 项目类别:
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