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本文引用的文献

1
Molecular chaperones: towards a characterization of the heat-shock protein 70 family.分子伴侣:向着热休克蛋白 70 家族的特征化研究。
Trends Cell Biol. 1997 Mar;7(3):129-33. doi: 10.1016/S0962-8924(96)10056-8.
2
Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
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Divergent transcriptional control of multidrug resistance genes in Saccharomyces cerevisiae.酿酒酵母中多药耐药基因的不同转录调控
J Biol Chem. 1998 Jan 23;273(4):2098-104. doi: 10.1074/jbc.273.4.2098.
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Chaperones get in touch: the Hip-Hop connection.伴侣蛋白建立联系:嘻哈音乐的关联
Trends Biochem Sci. 1997 Mar;22(3):87-92. doi: 10.1016/s0968-0004(97)01005-0.
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Functional specificity among Hsp70 molecular chaperones.热休克蛋白70分子伴侣之间的功能特异性。
Science. 1997 Jan 17;275(5298):387-9. doi: 10.1126/science.275.5298.387.
6
Anticancer drugs, ionophoric peptides, and steroids as substrates of the yeast multidrug transporter Pdr5p.抗癌药物、离子载体肽和类固醇作为酵母多药转运蛋白Pdr5p的底物。
J Biol Chem. 1996 Dec 6;271(49):31543-8. doi: 10.1074/jbc.271.49.31543.
7
Multiple Pdr1p/Pdr3p binding sites are essential for normal expression of the ATP binding cassette transporter protein-encoding gene PDR5.多个Pdr1p/Pdr3p结合位点对于ATP结合盒转运蛋白编码基因PDR5的正常表达至关重要。
J Biol Chem. 1996 Sep 20;271(38):23049-54. doi: 10.1074/jbc.271.38.23049.
8
Interactions of p60, a mediator of progesterone receptor assembly, with heat shock proteins hsp90 and hsp70.孕酮受体组装介质p60与热休克蛋白hsp90和hsp70的相互作用。
Mol Endocrinol. 1996 Jun;10(6):682-93. doi: 10.1210/mend.10.6.8776728.
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Msn2p, a zinc finger DNA-binding protein, is the transcriptional activator of the multistress response in Saccharomyces cerevisiae.Msn2p是一种锌指DNA结合蛋白,是酿酒酵母中多重应激反应的转录激活因子。
Proc Natl Acad Sci U S A. 1996 Jun 11;93(12):5777-82. doi: 10.1073/pnas.93.12.5777.
10
The Saccharomyces cerevisiae zinc finger proteins Msn2p and Msn4p are required for transcriptional induction through the stress response element (STRE).酿酒酵母锌指蛋白Msn2p和Msn4p是通过应激反应元件(STRE)进行转录诱导所必需的。
EMBO J. 1996 May 1;15(9):2227-35.

酿酒酵母中一种热休克蛋白70(Hsp70)对转录因子Pdr1p功能的调控

Regulation of transcription factor Pdr1p function by an Hsp70 protein in Saccharomyces cerevisiae.

作者信息

Hallstrom T C, Katzmann D J, Torres R J, Sharp W J, Moye-Rowley W S

机构信息

Department of Physiology, University of Iowa, Iowa City 52242, USA.

出版信息

Mol Cell Biol. 1998 Mar;18(3):1147-55. doi: 10.1128/MCB.18.3.1147.

DOI:10.1128/MCB.18.3.1147
PMID:9488429
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC108827/
Abstract

Multiple or pleiotropic drug resistance in the yeast Saccharomyces cerevisiae requires the expression of several ATP binding cassette transporter-encoding genes under the control of the zinc finger-containing transcription factor Pdrlp. The ATP binding cassette transporter-encoding genes regulated by Pdrlp include PDR5 and YOR1, which are required for normal cycloheximide and oligomycin tolerances, respectively. We have isolated a new member of the PDR gene family that encodes a member of the Hsp70 family of proteins found in this organism. This gene has been designated PDR13 and is required for normal growth. Overexpression of Pdr13p leads to an increase in both the expression of PDR5 and YOR1 and a corresponding enhancement in drug resistance. Pdr13p requires the presence of both the PDR1 structural gene and the Pdr1p binding sites in target promoters to mediate its effect on drug resistance and gene expression. A dominant, gain-of-function mutant allele of PDR13 was isolated and shown to have the same phenotypic effects as when the gene is present on a 2microm plasmid. Genetic and Western blotting experiments indicated that Pdr13p exerts its effect on Pdr1p at a posttranslational step. These data support the view that Pdr13p influences pleiotropic drug resistance by enhancing the function of the transcriptional regulatory protein Pdr1p.

摘要

酿酒酵母中的多重或多效性耐药需要在含锌指转录因子Pdr1p的控制下表达几个编码ATP结合盒转运蛋白的基因。受Pdr1p调控的编码ATP结合盒转运蛋白的基因包括PDR5和YOR1,它们分别是正常耐受环己酰亚胺和寡霉素所必需的。我们分离出了PDR基因家族的一个新成员,它编码该生物体中发现的Hsp70蛋白家族的一个成员。这个基因被命名为PDR13,是正常生长所必需的。Pdr13p的过表达导致PDR5和YOR1的表达增加以及相应的耐药性增强。Pdr13p需要PDR1结构基因和靶启动子中的Pdr1p结合位点同时存在,才能介导其对耐药性和基因表达的影响。分离出了一个显性的、功能获得性的PDR13突变等位基因,并且显示其具有与该基因存在于2μm质粒上时相同的表型效应。遗传和蛋白质印迹实验表明,Pdr13p在翻译后步骤对Pdr1p发挥作用。这些数据支持这样一种观点,即Pdr13p通过增强转录调节蛋白Pdr1p的功能来影响多效性耐药。