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大肠杆菌多核苷酸磷酸化酶mRNA的差异降解

Differential degradation of the Escherichia coli polynucleotide phosphorylase mRNA.

作者信息

Takata R, Izuhara M, Hori K

机构信息

Department of Biology, Saga Medical School, Japan.

出版信息

Nucleic Acids Res. 1989 Sep 25;17(18):7441-51. doi: 10.1093/nar/17.18.7441.

DOI:10.1093/nar/17.18.7441
PMID:2477797
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC334822/
Abstract

The transcript covering pnp, the gene encoding polynucleotide phosphorylase, is processed by RNaseIII at the 5'-upstream site of the pnp gene. In the RNaseIII-deficient strain, three species of the unprocessed transcript with different lengths could be detected. In this study, the stability of each transcript was analyzed by SI nuclease protection assay. The results show that the half-lives of the unprocessed transcripts are 8 min, whereas the half-life of the processed transcript is 1.5 min. It is also shown that the 5' segment of the unprocessed transcripts is more stable than the middle or the 3' segment.

摘要

覆盖多核苷酸磷酸化酶(PNP)编码基因pnp的转录本在pnp基因5'上游位点被RNaseIII加工。在RNaseIII缺陷型菌株中,可以检测到三种不同长度的未加工转录本。在本研究中,通过SI核酸酶保护试验分析了每种转录本的稳定性。结果表明,未加工转录本的半衰期为8分钟,而加工后转录本的半衰期为1.5分钟。还表明,未加工转录本的5'片段比中间或3'片段更稳定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f06/334822/394b6306aa6d/nar00135-0301-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f06/334822/62029caadf86/nar00135-0298-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f06/334822/e374b78142d8/nar00135-0300-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f06/334822/394b6306aa6d/nar00135-0301-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f06/334822/62029caadf86/nar00135-0298-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f06/334822/e374b78142d8/nar00135-0300-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f06/334822/394b6306aa6d/nar00135-0301-a.jpg

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1
Differential degradation of the Escherichia coli polynucleotide phosphorylase mRNA.大肠杆菌多核苷酸磷酸化酶mRNA的差异降解
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本文引用的文献

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Nucleotide sequence of the gene for Escherichia coli ribosomal protein S15 (rpsO).大肠杆菌核糖体蛋白S15(rpsO)基因的核苷酸序列。
Mol Gen Genet. 1984;197(2):225-9. doi: 10.1007/BF00330967.
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Growth-rate dependent regulation of mRNA stability in Escherichia coli.大肠杆菌中mRNA稳定性的生长速率依赖性调控。
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mRNA processing in Escherichia coli: an activity encoded by the host processes bacteriophage f1 mRNAs.大肠杆菌中的信使核糖核酸加工:宿主编码的一种活性对噬菌体f1信使核糖核酸进行加工。
RNA测序鉴定了[具体内容]中的新RNase III切割位点,并揭示了对mRNA的调控增加。
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Autogenous regulation of Escherichia coli polynucleotide phosphorylase expression revisited.大肠杆菌多核苷酸磷酸化酶表达的自体调节再探讨。
J Bacteriol. 2009 Mar;191(6):1738-48. doi: 10.1128/JB.01524-08. Epub 2009 Jan 9.
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Complex regulation of the organic hydroperoxide resistance gene (ohr) from Xanthomonas involves OhrR, a novel organic peroxide-inducible negative regulator, and posttranscriptional modifications.来自黄单胞菌属的有机氢过氧化物抗性基因(ohr)的复杂调控涉及OhrR,一种新型的有机过氧化物诱导型负调控因子,以及转录后修饰。
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Polynucleotide phosphorylase of Escherichia coli induces the degradation of its RNase III processed messenger by preventing its translation.大肠杆菌的多核苷酸磷酸化酶通过阻止其核糖核酸酶III加工的信使核糖核酸的翻译来诱导其降解。
Nucleic Acids Res. 1994 Feb 11;22(3):397-403. doi: 10.1093/nar/22.3.397.
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Cloning and sequencing of an Escherichia coli K12 gene which encodes a polypeptide having similarity to the human ferritin H subunit.编码与人类铁蛋白H亚基具有相似性的多肽的大肠杆菌K12基因的克隆与测序。
Mol Gen Genet. 1991 Mar;225(3):510-3. doi: 10.1007/BF00261694.
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Processing in the 5' region of the pnp transcript facilitates the site-specific endonucleolytic cleavages of mRNA.在pnp转录本5'区域的加工促进了mRNA的位点特异性内切核酸酶切割。
Nucleic Acids Res. 1992 Feb 25;20(4):847-50. doi: 10.1093/nar/20.4.847.
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The first step in the functional inactivation of the Escherichia coli polynucleotide phosphorylase messenger is a ribonuclease III processing at the 5' end.大肠杆菌多核苷酸磷酸化酶信使功能失活的第一步是在5'端进行核糖核酸酶III加工。
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Site-specific endonucleolytic cleavages and the regulation of stability of E. coli ompA mRNA.大肠杆菌ompA mRNA的位点特异性内切核酸酶切割及稳定性调控
Cell. 1988 Mar 25;52(6):893-901. doi: 10.1016/0092-8674(88)90431-x.
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