• 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

酿酒酵母中一条新型热休克应激调节途径的顺式和反式成分的鉴定。

Identification of cis and trans components of a novel heat shock stress regulatory pathway in Saccharomyces cerevisiae.

作者信息

Kobayashi N, McEntee K

机构信息

Department of Biological Chemistry, University of California Los Angeles, School of Medicine 90024.

出版信息

Mol Cell Biol. 1993 Jan;13(1):248-56. doi: 10.1128/mcb.13.1.248-256.1993.

DOI:10.1128/mcb.13.1.248-256.1993
PMID:8417330
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC358904/
Abstract

The stress-responsive DDR2 gene (previously called DDRA2) of Saccharomyces cerevisiae is transcribed at elevated levels following stress caused by heat shock or DNA damage. Previously, we identified a 51-bp promoter fragment, oligo31/32, which conferred heat shock inducibility on the heterologous CYC1-lacZ reporter gene in S. cerevisiae (N. Kobayashi and K. McEntee, Proc. Natl. Acad. Sci. USA 87:6550-6554, 1990). Using a series of synthetic oligonucleotides, we have identified a pentanucleotide, CCCCT (C4T), as an essential component of this stress response sequence. This element is not a binding site for the well-characterized heat shock transcription factor which recognizes a distinct cis-acting heat shock element in the promoters of many heat shock genes. Here we demonstrate the ability of oligonucleotides containing the C4T sequence to confer heat shock inducibility on the reporter gene and show that the presence of two such elements produces more than additive effects on induction. Gel retardation experiments have been used to demonstrate specific complex formation between C4T-containing fragments and one or more yeast proteins. Formation of these complexes was not competed by fragments containing mutations in the C4T sequence nor by heat shock element-containing competitor DNAs. Fragments containing the C4T element bound to a single 140-kDa polypeptide, distinct from heat shock transcription factors in yeast crude extracts. These experiments identify key cis- and trans-acting components of a novel heat shock stress response pathway in S. cerevisiae.

摘要

酿酒酵母的应激反应性DDR2基因(以前称为DDRA2)在热休克或DNA损伤引起的应激后转录水平升高。此前,我们鉴定出一个51bp的启动子片段oligo31/32,它赋予酿酒酵母中异源CYC1-lacZ报告基因热休克诱导性(N. 小林和K. 麦肯蒂,《美国国家科学院院刊》87:6550 - 6554,1990)。使用一系列合成寡核苷酸,我们确定了一个五核苷酸CCCCT(C4T)作为该应激反应序列的一个必需成分。这个元件不是已充分表征的热休克转录因子的结合位点,该转录因子识别许多热休克基因启动子中一个不同的顺式作用热休克元件。在这里,我们证明了含有C4T序列的寡核苷酸赋予报告基因热休克诱导性的能力,并表明两个这样的元件的存在对诱导产生的效应大于相加效应。凝胶阻滞实验已用于证明含C4T的片段与一种或多种酵母蛋白之间形成特异性复合物。这些复合物的形成既不被C4T序列中含有突变的片段竞争,也不被含热休克元件的竞争DNA竞争。含有C4T元件的片段与一种单一的140kDa多肽结合,该多肽不同于酵母粗提物中的热休克转录因子。这些实验确定了酿酒酵母中一条新型热休克应激反应途径的关键顺式和反式作用成分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85a2/358904/7d4d35699258/molcellb00013-0281-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85a2/358904/a33b5d0a4399/molcellb00013-0280-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85a2/358904/01e1e51f1cd8/molcellb00013-0280-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85a2/358904/7d4d35699258/molcellb00013-0281-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85a2/358904/a33b5d0a4399/molcellb00013-0280-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85a2/358904/01e1e51f1cd8/molcellb00013-0280-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85a2/358904/7d4d35699258/molcellb00013-0281-a.jpg

相似文献

1
Identification of cis and trans components of a novel heat shock stress regulatory pathway in Saccharomyces cerevisiae.酿酒酵母中一条新型热休克应激调节途径的顺式和反式成分的鉴定。
Mol Cell Biol. 1993 Jan;13(1):248-56. doi: 10.1128/mcb.13.1.248-256.1993.
2
The Saccharomyces cerevisiae HSP12 gene is activated by the high-osmolarity glycerol pathway and negatively regulated by protein kinase A.酿酒酵母HSP12基因由高渗甘油途径激活,并受到蛋白激酶A的负调控。
Mol Cell Biol. 1995 Nov;15(11):6232-45. doi: 10.1128/MCB.15.11.6232.
3
The Skn7 response regulator of Saccharomyces cerevisiae interacts with Hsf1 in vivo and is required for the induction of heat shock genes by oxidative stress.酿酒酵母的Skn7应答调节因子在体内与Hsf1相互作用,并且是氧化应激诱导热休克基因所必需的。
Mol Biol Cell. 2000 Jul;11(7):2335-47. doi: 10.1091/mbc.11.7.2335.
4
Stress induction of HSP30, the plasma membrane heat shock protein gene of Saccharomyces cerevisiae, appears not to use known stress-regulated transcription factors.酿酒酵母质膜热休克蛋白基因HSP30的应激诱导似乎不涉及已知的应激调节转录因子。
Microbiology (Reading). 1999 Jan;145 ( Pt 1):231-239. doi: 10.1099/13500872-145-1-231.
5
A 22 bp cis-acting element is necessary and sufficient for the induction of the yeast KAR2 (BiP) gene by unfolded proteins.一个22个碱基对的顺式作用元件对于未折叠蛋白诱导酵母KAR2(BiP)基因而言是必需且充分的。
EMBO J. 1992 Jul;11(7):2583-93. doi: 10.1002/j.1460-2075.1992.tb05323.x.
6
Identification of a novel class of target genes and a novel type of binding sequence of heat shock transcription factor in Saccharomyces cerevisiae.酿酒酵母中一类新型靶基因及热休克转录因子新型结合序列的鉴定。
J Biol Chem. 2005 Mar 25;280(12):11911-9. doi: 10.1074/jbc.M411256200. Epub 2005 Jan 11.
7
The promoter region of the yeast KAR2 (BiP) gene contains a regulatory domain that responds to the presence of unfolded proteins in the endoplasmic reticulum.酵母KAR2(BiP)基因的启动子区域包含一个调控结构域,该结构域可对内质网中未折叠蛋白的存在做出反应。
Mol Cell Biol. 1993 Feb;13(2):877-90. doi: 10.1128/mcb.13.2.877-890.1993.
8
A critical role for heat shock transcription factor in establishing a nucleosome-free region over the TATA-initiation site of the yeast HSP82 heat shock gene.热休克转录因子在酵母HSP82热休克基因的TATA起始位点上建立无核小体区域中起关键作用。
EMBO J. 1993 Oct;12(10):3931-45. doi: 10.1002/j.1460-2075.1993.tb06071.x.
9
Saccharomyces cerevisiae HSP70 heat shock elements are functionally distinct.酿酒酵母HSP70热休克元件功能各异。
Mol Cell Biol. 1993 Sep;13(9):5637-46. doi: 10.1128/mcb.13.9.5637-5646.1993.
10
Evidence for a heat shock transcription factor-independent mechanism for heat shock induction of transcription in Saccharomyces cerevisiae.酿酒酵母中热休克诱导转录的热休克转录因子非依赖机制的证据。
Proc Natl Acad Sci U S A. 1990 Sep;87(17):6550-4. doi: 10.1073/pnas.87.17.6550.

引用本文的文献

1
An adaptive biomolecular condensation response is conserved across environmentally divergent species.适应生物分子凝聚反应在环境差异较大的物种中是保守的。
Nat Commun. 2024 Apr 11;15(1):3127. doi: 10.1038/s41467-024-47355-9.
2
An adaptive biomolecular condensation response is conserved across environmentally divergent species.适应性生物分子凝聚反应在环境差异较大的物种中是保守的。
bioRxiv. 2023 Jul 29:2023.07.28.551061. doi: 10.1101/2023.07.28.551061.
3
Transcriptome Analysis of Bread Wheat Genotype KRL3-4 Provides a New Insight Into Regulatory Mechanisms Associated With Sodicity (High pH) Tolerance.

本文引用的文献

1
A regulatory upstream promoter element in the Drosophila hsp 70 heat-shock gene.果蝇热休克蛋白70(hsp 70)基因中的一个调控上游启动子元件。
Cell. 1982 Sep;30(2):517-28. doi: 10.1016/0092-8674(82)90249-5.
2
Two protein-binding sites in chromatin implicated in the activation of heat-shock genes.染色质中与热休克基因激活有关的两个蛋白质结合位点。
Nature. 1984;309(5965):229-34. doi: 10.1038/309229a0.
3
groEL and dnaK genes of Escherichia coli are induced by UV irradiation and nalidixic acid in an htpR+-dependent fashion.大肠杆菌的groEL和dnaK基因以依赖htpR⁺的方式被紫外线照射和萘啶酸诱导。
面包小麦基因型KRL3-4的转录组分析为与耐盐碱(高pH值)相关的调控机制提供了新见解。
Front Genet. 2022 Feb 9;12:782366. doi: 10.3389/fgene.2021.782366. eCollection 2021.
4
Identification and expression analysis of genes in tea plant exposed to anthracnose pathogen and drought stresses.茶树炭疽病菌和干旱胁迫相关基因的鉴定与表达分析。
Plant Signal Behav. 2021 Dec 2;16(12):1976547. doi: 10.1080/15592324.2021.1976547. Epub 2021 Oct 11.
5
Sporulation in .在……中形成芽孢
J Fungi (Basel). 2020 Aug 29;6(3):157. doi: 10.3390/jof6030157.
6
Cellular and metabolic engineering of oleaginous yeast for bioconversion of hydrophobic substrates into high-value products.产油酵母的细胞与代谢工程用于将疏水底物生物转化为高价值产品。
Eng Life Sci. 2019 Feb 27;19(6):423-443. doi: 10.1002/elsc.201800147. eCollection 2019 Jun.
7
Multi-kinase control of environmental stress responsive transcription.多激酶对环境应激反应转录的调控。
PLoS One. 2020 Mar 11;15(3):e0230246. doi: 10.1371/journal.pone.0230246. eCollection 2020.
8
Global Transcriptional Programs in Archaea Share Features with the Eukaryotic Environmental Stress Response.古菌的全球转录程序与真核生物的环境应激反应具有共同特征。
J Mol Biol. 2019 Sep 20;431(20):4147-4166. doi: 10.1016/j.jmb.2019.07.029. Epub 2019 Aug 19.
9
Genome analyses of the new model protist Euplotes vannus focusing on genome rearrangement and resistance to environmental stressors.对新型原生动物真涡虫的基因组分析,重点关注基因组重排和对环境胁迫的抗性。
Mol Ecol Resour. 2019 Sep;19(5):1292-1308. doi: 10.1111/1755-0998.13023. Epub 2019 Jun 6.
10
The Anti-Oxidant Defense System of the Marine Polar Ciliate Euplotes nobilii: Characterization of the MsrB Gene Family.海洋极地纤毛虫高贵游仆虫的抗氧化防御系统:MsrB基因家族的特征
Biology (Basel). 2017 Jan 18;6(1):4. doi: 10.3390/biology6010004.
Proc Natl Acad Sci U S A. 1984 Mar;81(5):1499-503. doi: 10.1073/pnas.81.5.1499.
4
Purification and properties of Drosophila heat shock activator protein.果蝇热休克激活蛋白的纯化及特性
Science. 1987 Nov 27;238(4831):1247-53. doi: 10.1126/science.3685975.
5
Induction of sequence-specific binding of Drosophila heat shock activator protein without protein synthesis.果蝇热休克激活蛋白序列特异性结合的诱导,无需蛋白质合成。
Nature. 1987;327(6124):727-30. doi: 10.1038/327727a0.
6
Affinity purification of sequence-specific DNA binding proteins.序列特异性DNA结合蛋白的亲和纯化
Proc Natl Acad Sci U S A. 1986 Aug;83(16):5889-93. doi: 10.1073/pnas.83.16.5889.
7
Accurate initiation at RNA polymerase II promoters in extracts from Saccharomyces cerevisiae.酿酒酵母提取物中RNA聚合酶II启动子的准确起始。
Proc Natl Acad Sci U S A. 1987 Dec;84(24):8839-43. doi: 10.1073/pnas.84.24.8839.
8
Purification and characterization of a heat-shock element binding protein from yeast.酵母热休克元件结合蛋白的纯化与鉴定
EMBO J. 1987 Oct;6(10):3035-41. doi: 10.1002/j.1460-2075.1987.tb02609.x.
9
Heat shock factor is regulated differently in yeast and HeLa cells.热休克因子在酵母细胞和人宫颈癌细胞(HeLa细胞)中的调控方式不同。
Nature. 1987;329(6134):81-4. doi: 10.1038/329081a0.
10
Purified human factor activates heat shock promoter in a HeLa cell-free transcription system.纯化的人因子在无细胞的HeLa转录系统中激活热休克启动子。
J Biol Chem. 1988 Dec 25;263(36):19734-9.