• 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

多顺反子mRNA的加工需要一个5'顺式元件和活跃的翻译过程。

Processing of a polycistronic mRNA requires a 5' cis element and active translation.

作者信息

Alifano P, Piscitelli C, Blasi V, Rivellini F, Nappo A G, Bruni C B, Carlomagno M S

机构信息

Dipartimento di Biologia e Patologia Cellulare e Molecolare, Centro di Endocrinologia ed Oncologia Sperimentale del Consiglio Nazionale delle Richerche, Università di Napoli, Italy.

出版信息

Mol Microbiol. 1992 Mar;6(6):787-98. doi: 10.1111/j.1365-2958.1992.tb01529.x.

DOI:10.1111/j.1365-2958.1992.tb01529.x
PMID:1374148
Abstract

We have characterized a major processed species of mRNA in the his operon of Salmonella typhimurium. In vivo and in vitro analyses of the his transcripts from wild-type and mutant strains using S1 nuclease protection assays, measurements of RNA stability, deletion mapping, gel retardation, and in vitro translation assays demonstrate that the distal portion of the polycistronic his mRNA is processed, resulting in increased stability. The processing event requires an upstream cis-acting element and translation of the cistron immediately downstream of the 5' end of the processed species. The cistrons contained in this segment are also independently transcribed from an internal promoter which is maximally active in the absence of readthrough transcription from the primary promoter.

摘要

我们已对鼠伤寒沙门氏菌组氨酸操纵子中一种主要的加工后mRNA种类进行了表征。利用S1核酸酶保护分析、RNA稳定性测量、缺失定位、凝胶阻滞和体外翻译分析,对野生型和突变株的组氨酸转录本进行体内和体外分析,结果表明,多顺反子组氨酸mRNA的远端部分被加工,从而提高了稳定性。加工事件需要一个上游顺式作用元件以及加工后物种5'端紧邻的顺反子的翻译。该片段中包含的顺反子也从一个内部启动子独立转录,该启动子在没有来自初级启动子的通读转录时活性最高。

相似文献

1
Processing of a polycistronic mRNA requires a 5' cis element and active translation.多顺反子mRNA的加工需要一个5'顺式元件和活跃的翻译过程。
Mol Microbiol. 1992 Mar;6(6):787-98. doi: 10.1111/j.1365-2958.1992.tb01529.x.
2
Ribonuclease E provides substrates for ribonuclease P-dependent processing of a polycistronic mRNA.核糖核酸酶E为多顺反子信使核糖核酸的核糖核酸酶P依赖性加工提供底物。
Genes Dev. 1994 Dec 15;8(24):3021-31. doi: 10.1101/gad.8.24.3021.
3
Transcriptional analysis of the rpoE gene encoding extracytoplasmic stress response sigma factor sigmaE in Salmonella enterica serovar Typhimurium.鼠伤寒沙门氏菌中编码胞质外应激反应σ因子σE的rpoE基因的转录分析。
FEMS Microbiol Lett. 2003 Sep 26;226(2):307-14. doi: 10.1016/S0378-1097(03)00600-1.
4
Sequence, regulation, and functions of fis in Salmonella typhimurium.鼠伤寒沙门氏菌中fis的序列、调控及功能
J Bacteriol. 1995 Apr;177(8):2021-32. doi: 10.1128/jb.177.8.2021-2032.1995.
5
Functional analysis of the tdcABC promoter of Escherichia coli: roles of TdcA and TdcR.大肠杆菌tdcABC启动子的功能分析:TdcA和TdcR的作用
J Bacteriol. 1994 Oct;176(20):6214-20. doi: 10.1128/jb.176.20.6214-6220.1994.
6
Transcription of the stability operon of IncFII plasmid NR1.IncFII 质粒 NR1 稳定性操纵子的转录
J Bacteriol. 1991 Apr;173(7):2378-84. doi: 10.1128/jb.173.7.2378-2384.1991.
7
A transcriptional silencer downstream of the promoter in the osmotically controlled proU operon of Salmonella typhimurium.鼠伤寒沙门氏菌渗透压调控的proU操纵子中启动子下游的转录沉默子。
Proc Natl Acad Sci U S A. 1992 Apr 1;89(7):3140-4. doi: 10.1073/pnas.89.7.3140.
8
Expression of cnf1 by Escherichia coli J96 involves a large upstream DNA region including the hlyCABD operon, and is regulated by the RfaH protein.大肠杆菌J96中细胞毒素坏死因子1(cnf1)的表达涉及一个包括溶血素基因hlyCABD操纵子的大型上游DNA区域,并受RfaH蛋白调控。
Mol Microbiol. 2003 Mar;47(6):1653-67. doi: 10.1046/j.1365-2958.2003.03391.x.
9
Convergently functional, Rho-independent terminator in Salmonella typhimurium.鼠伤寒沙门氏菌中具有收敛功能的、不依赖 Rho 因子的终止子。
J Bacteriol. 1985 Jul;163(1):362-8. doi: 10.1128/jb.163.1.362-368.1985.
10
Cleavage by RNase III in the transcripts of the met Y-nus-A-infB operon of Escherichia coli releases the tRNA and initiates the decay of the downstream mRNA.大肠杆菌met Y-nus-A-infB操纵子转录本中的核糖核酸酶III切割会释放出转运RNA,并引发下游信使核糖核酸的降解。
J Mol Biol. 1989 Nov 20;210(2):293-302. doi: 10.1016/0022-2836(89)90331-8.

引用本文的文献

1
Biosynthesis of Histidine.组氨酸的生物合成
EcoSal Plus. 2009 Aug;3(2). doi: 10.1128/ecosalplus.3.6.1.9.
2
Post-transcriptional control of gene expression: bacterial mRNA degradation.转录后基因表达调控:细菌 mRNA 降解。
World J Microbiol Biotechnol. 1993 Jul;9(4):421-32. doi: 10.1007/BF00328030.
3
Histidine biosynthesis, its regulation and biotechnological application in Corynebacterium glutamicum.谷氨酸棒杆菌中组氨酸的生物合成、调控及其生物技术应用。
Microb Biotechnol. 2014 Jan;7(1):5-25. doi: 10.1111/1751-7915.12055. Epub 2013 Apr 25.
4
Short RNA half-lives in the slow-growing marine cyanobacterium Prochlorococcus.在生长缓慢的海洋蓝藻聚球藻中,短 RNA 的半衰期较短。
Genome Biol. 2010;11(5):R54. doi: 10.1186/gb-2010-11-5-r54. Epub 2010 May 19.
5
Post-transcriptional processing of the LEE4 operon in enterohaemorrhagic Escherichia coli.肠出血性大肠杆菌中LEE4操纵子的转录后加工
Mol Microbiol. 2009 Jan;71(2):273-90. doi: 10.1111/j.1365-2958.2008.06530.x. Epub 2008 Nov 4.
6
Detection of low-level promoter activity within open reading frame sequences of Escherichia coli.大肠杆菌开放阅读框序列内低水平启动子活性的检测
Nucleic Acids Res. 2005 Oct 31;33(19):6268-76. doi: 10.1093/nar/gki928. Print 2005.
7
Processing endoribonucleases and mRNA degradation in bacteria.细菌中的内切核糖核酸酶加工与mRNA降解
J Bacteriol. 2002 Sep;184(17):4645-57; discussion 4665. doi: 10.1128/JB.184.17.4645-4657.2002.
8
The global regulator CsrA of Escherichia coli is a specific mRNA-binding protein.大肠杆菌的全局调控因子CsrA是一种特异性mRNA结合蛋白。
J Bacteriol. 1997 Jul;179(14):4639-42. doi: 10.1128/jb.179.14.4639-4642.1997.
9
Histidine biosynthetic pathway and genes: structure, regulation, and evolution.组氨酸生物合成途径与基因:结构、调控及进化
Microbiol Rev. 1996 Mar;60(1):44-69. doi: 10.1128/mr.60.1.44-69.1996.
10
Differential mRNA decay within the transfer operon of plasmid R1: identification and analysis of an intracistronic mRNA stabilizer.质粒R1转移操纵子内的mRNA差异降解:顺反子内mRNA稳定剂的鉴定与分析。
Mol Gen Genet. 1996 Mar 7;250(4):466-76. doi: 10.1007/BF02174035.