• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

RHO基因产物,即假定的小GTP结合蛋白,对于酿酒酵母中CAL1/CDC43基因产物(一种蛋白质香叶基香叶基转移酶)的激活很重要。

RHO gene products, putative small GTP-binding proteins, are important for activation of the CAL1/CDC43 gene product, a protein geranylgeranyltransferase in Saccharomyces cerevisiae.

作者信息

Qadota H, Ishii I, Fujiyama A, Ohya Y, Anraku Y

机构信息

Department of Biology, Faculty of Science, University of Tokyo, Japan.

出版信息

Yeast. 1992 Sep;8(9):735-41. doi: 10.1002/yea.320080906.

DOI:10.1002/yea.320080906
PMID:1441750
Abstract

Two multicopy suppressors of the cal1-1 mutation in the yeast Saccharomyces cerevisiae have been isolated and characterized. They are identical to the yeast RHO1 and RHO2 genes, which encode putative small GTP-binding proteins. Multiple copies of either RHO gene suppressed temperature-sensitive growth of the cal1-1 mutant but did not suppress the cal1 null mutant. Genetic analysis suggests that overproduction of either RHO gene product acts for activation of the CAL1 gene product.

摘要

已分离并鉴定出酿酒酵母中cal1-1突变的两个多拷贝抑制子。它们与酵母RHO1和RHO2基因相同,这两个基因编码假定的小GTP结合蛋白。任一RHO基因的多个拷贝都抑制了cal1-1突变体的温度敏感生长,但不抑制cal1缺失突变体。遗传分析表明,任一RHO基因产物的过量表达都起到激活CAL1基因产物的作用。

相似文献

1
RHO gene products, putative small GTP-binding proteins, are important for activation of the CAL1/CDC43 gene product, a protein geranylgeranyltransferase in Saccharomyces cerevisiae.RHO基因产物,即假定的小GTP结合蛋白,对于酿酒酵母中CAL1/CDC43基因产物(一种蛋白质香叶基香叶基转移酶)的激活很重要。
Yeast. 1992 Sep;8(9):735-41. doi: 10.1002/yea.320080906.
2
Mutational analysis of the beta-subunit of yeast geranylgeranyl transferase I.酵母香叶基香叶基转移酶Iβ亚基的突变分析
Mol Gen Genet. 1996 Aug 27;252(1-2):1-10.
3
Rom1p and Rom2p are GDP/GTP exchange proteins (GEPs) for the Rho1p small GTP binding protein in Saccharomyces cerevisiae.Rom1p和Rom2p是酿酒酵母中Rho1p小GTP结合蛋白的GDP/GTP交换蛋白(GEP)。
EMBO J. 1996 May 1;15(9):2196-207.
4
Multicopy suppressors of the sly1 temperature-sensitive mutation in the ER-Golgi vesicular transport in Saccharomyces cerevisiae.酿酒酵母内质网-高尔基体囊泡运输中sly1温度敏感突变的多拷贝抑制子
Yeast. 2001 Aug;18(11):1003-14. doi: 10.1002/yea.747.
5
Association of the Rho family small GTP-binding proteins with Rho GDP dissociation inhibitor (Rho GDI) in Saccharomyces cerevisiae.酿酒酵母中Rho家族小GTP结合蛋白与Rho GDP解离抑制剂(Rho GDI)的关联。
Oncogene. 1997 Jul 24;15(4):417-22. doi: 10.1038/sj.onc.1201194.
6
Cell wall integrity modulates RHO1 activity via the exchange factor ROM2.细胞壁完整性通过交换因子ROM2调节RHO1活性。
EMBO J. 1998 Apr 15;17(8):2235-45. doi: 10.1093/emboj/17.8.2235.
7
Shs1p: a novel member of septin that interacts with spa2p, involved in polarized growth in saccharomyces cerevisiae.Shs1p:一种与spa2p相互作用的septin新成员,参与酿酒酵母的极性生长。
Biochem Biophys Res Commun. 1998 Oct 29;251(3):732-6. doi: 10.1006/bbrc.1998.9541.
8
Protein geranylgeranyltransferase of Saccharomyces cerevisiae is specific for Cys-Xaa-Xaa-Leu motif proteins and requires the CDC43 gene product but not the DPR1 gene product.酿酒酵母的蛋白质香叶基香叶基转移酶对Cys-Xaa-Xaa-Leu基序蛋白具有特异性,并且需要CDC43基因产物,但不需要DPR1基因产物。
Proc Natl Acad Sci U S A. 1991 May 15;88(10):4448-52. doi: 10.1073/pnas.88.10.4448.
9
GPR1 encodes a putative G protein-coupled receptor that associates with the Gpa2p Galpha subunit and functions in a Ras-independent pathway.GPR1编码一种假定的G蛋白偶联受体,该受体与Gpa2p Gα亚基相关联,并在一条不依赖Ras的途径中发挥作用。
EMBO J. 1998 Apr 1;17(7):1996-2007. doi: 10.1093/emboj/17.7.1996.
10
Control of cellular morphogenesis by the Ip12/Bem2 GTPase-activating protein: possible role of protein phosphorylation.由Ip12/Bem2 GTP酶激活蛋白控制细胞形态发生:蛋白质磷酸化的可能作用。
J Cell Biol. 1994 Dec;127(5):1381-94. doi: 10.1083/jcb.127.5.1381.

引用本文的文献

1
The Role of the Cell Integrity Pathway in Septum Assembly in Yeast.细胞完整性途径在酵母隔膜组装中的作用
J Fungi (Basel). 2021 Sep 6;7(9):729. doi: 10.3390/jof7090729.
2
Calcineurin Regulatory Subunit Calcium-Binding Domains Differentially Contribute to Calcineurin Signaling in .钙调神经磷酸酶调节亚基钙结合结构域对 中的钙调神经磷酸酶信号传递具有不同的贡献。
Genetics. 2018 Jul;209(3):801-813. doi: 10.1534/genetics.118.300911. Epub 2018 May 7.
3
The Late S-Phase Transcription Factor Hcm1 Is Regulated through Phosphorylation by the Cell Wall Integrity Checkpoint.
晚期S期转录因子Hcm1受细胞壁完整性检查点的磷酸化调控。
Mol Cell Biol. 2016 Jan 4;36(6):941-53. doi: 10.1128/MCB.00952-15.
4
Proteasome Impairment Induces Recovery of Mitochondrial Membrane Potential and an Alternative Pathway of Mitochondrial Fusion.蛋白酶体损伤诱导线粒体膜电位恢复及线粒体融合的替代途径。
Mol Cell Biol. 2015 Nov 9;36(2):347-62. doi: 10.1128/MCB.00920-15. Print 2016 Jan 15.
5
N-terminal α7 deletion of the proteasome 20S core particle substitutes for yeast PI31 function.蛋白酶体20S核心颗粒的N端α7缺失替代了酵母PI31的功能。
Mol Cell Biol. 2015 Jan;35(1):141-52. doi: 10.1128/MCB.00582-14. Epub 2014 Oct 20.
6
Profilin is required for Ca2+ homeostasis and Ca2+-modulated bud formation in yeast.丝状肌动蛋白结合蛋白对于酵母细胞内钙离子稳态和钙离子调控的出芽形成是必需的。
Mol Genet Genomics. 2013 Aug;288(7-8):317-28. doi: 10.1007/s00438-013-0752-x. Epub 2013 May 26.
7
Yos9p and Hrd1p mediate ER retention of misfolded proteins for ER-associated degradation.Yos9p 和 Hrd1p 介导错误折叠蛋白在 ER 中的滞留,以进行 ER 相关降解。
Mol Biol Cell. 2012 Apr;23(7):1283-93. doi: 10.1091/mbc.E11-08-0722. Epub 2012 Feb 1.
8
Roles of protein-disulfide isomerase-mediated disulfide bond formation of yeast Mnl1p in endoplasmic reticulum-associated degradation.蛋白质二硫键异构酶介导的酵母Mnl1p二硫键形成在内质网相关降解中的作用
J Biol Chem. 2009 May 1;284(18):11815-25. doi: 10.1074/jbc.M900813200. Epub 2009 Mar 11.
9
The PXL1 gene of Saccharomyces cerevisiae encodes a paxillin-like protein functioning in polarized cell growth.酿酒酵母的PXL1基因编码一种在极化细胞生长中起作用的桩蛋白样蛋白。
Mol Biol Cell. 2004 Apr;15(4):1904-17. doi: 10.1091/mbc.e04-01-0004. Epub 2004 Feb 6.
10
Posttranslational modifications required for cell surface localization and function of the fungal adhesin Aga1p.真菌粘附素Aga1p细胞表面定位和功能所需的翻译后修饰。
Eukaryot Cell. 2003 Oct;2(5):1099-114. doi: 10.1128/EC.2.5.1099-1114.2003.