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:
    2853596
  • 负责人:
  • 金额:
    $ 29.42万
  • 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 2003-03-31
  • 项目状态:
    已结题

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(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)

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ monograph.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ sciAawards.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ conferencePapers.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ patent.updateTime }}

ELIZABETH W JONES其他文献

ELIZABETH W JONES的其他文献

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

{{ 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:
    $ 29.42万
  • 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:
    $ 29.42万
  • 项目类别:
GENETICS STUDY SECTION
遗传学研究部分
  • 批准号:
    3555211
  • 财政年份:
    1990
  • 资助金额:
    $ 29.42万
  • 项目类别:
GENETICS STUDY SECTION
遗传学研究部分
  • 批准号:
    3555216
  • 财政年份:
    1990
  • 资助金额:
    $ 29.42万
  • 项目类别:
CELLULAR AND MOLECULAR BIOLOGY
细胞和分子生物学
  • 批准号:
    3538092
  • 财政年份:
    1983
  • 资助金额:
    $ 29.42万
  • 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:
    $ 29.42万
  • 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:
    $ 29.42万
  • 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:
    $ 29.42万
  • 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:
    6519047
  • 财政年份:
    1981
  • 资助金额:
    $ 29.42万
  • 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:
    $ 29.42万
  • 项目类别:

相似海外基金

Structural Analysis of a Metabolic Enzyme Complex: Insights into Coupling between Glycolysis and Fermentation
代谢酶复合物的结构分析:深入了解糖酵解与发酵之间的耦合
  • 批准号:
    23K05667
  • 财政年份:
    2023
  • 资助金额:
    $ 29.42万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Role of Multi-enzyme Complex in ApoBCL Secretion
多酶复合物在 ApoBCL 分泌中的作用
  • 批准号:
    10543873
  • 财政年份:
    2022
  • 资助金额:
    $ 29.42万
  • 项目类别:
Role of Multi-enzyme Complex in ApoBCL Secretion
多酶复合物在 ApoBCL 分泌中的作用
  • 批准号:
    10332597
  • 财政年份:
    2022
  • 资助金额:
    $ 29.42万
  • 项目类别:
Is a Hydrogenase-Like Enzyme Complex Lacking a Catalytic Center the Missing Link in the Respiratory Complexes?
缺乏催化中心的类似氢化酶的酶复合物是呼吸复合物中缺失的一环吗?
  • 批准号:
    21K20578
  • 财政年份:
    2021
  • 资助金额:
    $ 29.42万
  • 项目类别:
    Grant-in-Aid for Research Activity Start-up
Luminescence of carbon nanotube-enzyme complex and its application
碳纳米管-酶复合物的发光及其应用
  • 批准号:
    19H02539
  • 财政年份:
    2019
  • 资助金额:
    $ 29.42万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Elucidation of effective consecutive chemical reaction in cell with formation of supramolecular enzyme complex
阐明细胞内有效连续化学反应形成超分子酶复合物
  • 批准号:
    17H03092
  • 财政年份:
    2017
  • 资助金额:
    $ 29.42万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Conflict and Coevolution in a Plastid- Nuclear Enzyme Complex
质体-核酶复合物中的冲突和共同进化
  • 批准号:
    1713849
  • 财政年份:
    2017
  • 资助金额:
    $ 29.42万
  • 项目类别:
    Standard Grant
Construction and analysis of recombinant cyanobacterium expressing a chimeric enzyme complex for ethylene production
表达乙烯生产嵌合酶复合物的重组蓝细菌的构建和分析
  • 批准号:
    26850224
  • 财政年份:
    2014
  • 资助金额:
    $ 29.42万
  • 项目类别:
    Grant-in-Aid for Young Scientists (B)
Sequential enzyme complex formation on DNA
DNA 上连续形成酶复合物
  • 批准号:
    26630419
  • 财政年份:
    2014
  • 资助金额:
    $ 29.42万
  • 项目类别:
    Grant-in-Aid for Challenging Exploratory Research
Regulation and specificity of deubiquitylating enzyme complex
去泛素化酶复合物的调节和特异性
  • 批准号:
    8618909
  • 财政年份:
    2012
  • 资助金额:
    $ 29.42万
  • 项目类别:
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了