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Distribution of 5'-triphosphate termini on the mRNA of Escherichia coli.5'-三磷酸末端在大肠杆菌mRNA上的分布
J Bacteriol. 1989 Jan;171(1):141-7. doi: 10.1128/jb.171.1.141-147.1989.
2
Initiation characteristics for the synthesis of five T4 phage-specific messenger RNAs in vitro.体外合成五种T4噬菌体特异性信使核糖核酸的起始特征
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Development of an in vitro mRNA decay system for Escherichia coli: poly(A) polymerase I is necessary to trigger degradation.用于大肠杆菌的体外mRNA降解系统的开发:聚腺苷酸聚合酶I是触发降解所必需的。
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Incorporation of purine nucleoside 5'-[gamma-S]triphosphates as affinity probes for initiation of RNA synthesis in vitro.将嘌呤核苷5'-[γ-S]三磷酸掺入作为体外RNA合成起始的亲和探针。
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Structural characterization and in vitro processing of Escherichia coli ribosomal RNA transcripts containing 5- triphosphates, leader sequences, 16 S rRNA, and spacer tRNAs.含有5'-三磷酸、前导序列、16S核糖体RNA和间隔转运RNA的大肠杆菌核糖体RNA转录本的结构表征及体外加工
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In vivo transcription of rRNA operons in Escherichia coli initiates with purine nucleoside triphosphates at the first promoter and with CTP at the second promoter.在大肠杆菌中,rRNA操纵子的体内转录在第一个启动子处由嘌呤核苷三磷酸起始,在第二个启动子处由CTP起始。
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Initiation of RNA decay in Escherichia coli by 5' pyrophosphate removal.通过去除5'焦磷酸启动大肠杆菌中的RNA衰变。
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Mechanistic characterization of the 5'-triphosphate-dependent activation of PKR: lack of 5'-end nucleobase specificity, evidence for a distinct triphosphate binding site, and a critical role for the dsRBD.PKR 的 5'-三磷酸依赖性激活的机制特征:缺乏 5'-末端核苷碱基特异性,存在独特的三磷酸结合位点的证据,以及 dsRBD 的关键作用。
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Bacterial RNA mediates activation of caspase-1 and IL-1β release independently of TLRs 3, 7, 9 and TRIF but is dependent on UNC93B.细菌 RNA 通过 UNC93B 介导 caspase-1 和 IL-1β 的释放,而不依赖于 TLRs 3、7、9 和 TRIF。
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Mitochondrial antiviral signaling protein (MAVS) monitors commensal bacteria and induces an immune response that prevents experimental colitis.线粒体抗病毒信号蛋白(MAVS)监测共生菌,并诱导免疫反应,防止实验性结肠炎。
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MyD88 and STING signaling pathways are required for IRF3-mediated IFN-β induction in response to Brucella abortus infection.MyD88 和 STING 信号通路是布鲁氏菌感染诱导 IRF3 介导的 IFN-β 诱导所必需的。
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本文引用的文献

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The addition of 5' cap structures occurs early in hnRNA synthesis and prematurely terminated molecules are capped.5'帽结构的添加在核内不均一RNA(hnRNA)合成早期发生,并且提前终止的分子也会被加帽。
Cell. 1980 Jan;19(1):69-78. doi: 10.1016/0092-8674(80)90389-x.
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RNA processing in a unicellular microorganism: implications for eukaryotic cells.单细胞微生物中的RNA加工:对真核细胞的启示
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Compilation and analysis of Escherichia coli promoter DNA sequences.大肠杆菌启动子DNA序列的汇编与分析
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Direction of chain growth in enzymic RNA synthesis.酶促RNA合成中链生长的方向。
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The role of DNA in RNA synthesis, IX. Nucleoside triphosphate termini in RNA polymerase products.DNA在RNA合成中的作用,IX. RNA聚合酶产物中的核苷三磷酸末端。
Proc Natl Acad Sci U S A. 1965 Sep;54(3):815-22. doi: 10.1073/pnas.54.3.815.
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Mutants of Escherichia coli sensitive to antibiotics.对抗生素敏感的大肠杆菌突变体。
J Bacteriol. 1971 Aug;107(2):486-90. doi: 10.1128/jb.107.2.486-490.1971.
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Nucleoside triphosphate termini from RNA synthesized in vivo by Escherichia coli.大肠杆菌在体内合成的RNA中的核苷三磷酸末端。
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Use of Brij lysis as a general method to prepare polyribosomes from Escherichia coli.使用Brij裂解作为从大肠杆菌制备多核糖体的通用方法。
Biochim Biophys Acta. 1967 Dec 19;149(2):489-95. doi: 10.1016/0005-2787(67)90176-1.
9
Thymidine and thymine incorporation into deoxyribonucleic acid: inhibition and repression by uridine of thymidine phosphorylase of Escherichia coli.胸苷和胸腺嘧啶掺入脱氧核糖核酸:尿苷对大肠杆菌胸苷磷酸化酶的抑制和阻遏作用
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Biological decay of the 5'-triphosphate termini of the RNA of E. coli.大肠杆菌RNA 5'-三磷酸末端的生物衰变
Nature. 1974 Nov 1;252(5478):74-6. doi: 10.1038/252074a0.

5'-三磷酸末端在大肠杆菌mRNA上的分布

Distribution of 5'-triphosphate termini on the mRNA of Escherichia coli.

作者信息

Bieger C D, Nierlich D P

机构信息

Department of Microbiology, University of California, Los Angeles 90024.

出版信息

J Bacteriol. 1989 Jan;171(1):141-7. doi: 10.1128/jb.171.1.141-147.1989.

DOI:10.1128/jb.171.1.141-147.1989
PMID:2464575
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC209566/
Abstract

We have determined the distribution of 5'-nucleoside triphosphates on the RNA in Escherichia coli. These groups represent the initial nucleoside triphosphate incorporated when RNA polymerase initiates transcription. It was estimated that at least 15% of polysome-associated messengers had triphosphates. This was interpreted to mean that removal of the triphosphate or messenger leader is not necessary for the functioning of most mRNAs but that a substantial amount of messenger processing occurs in the polysome pool. We found that the ratio of GTP- to ATP-initiated messengers was about 2 to 1. Since prior work has indicated that G- and A-initiated RNAs decay at the same rate and since a compilation of messenger start sites shows an A preference, this value implies that there is a significant physiological selection of G-initiated transcripts. We also characterized the 5'-terminal groups on RNAs in other fractions. A small amount was found associated with 30S ribosomes, presumably in initiation complexes; such complexes have not previously been detected in situ. In addition, it was concluded that the 5' terminus of rRNA precursors is processed more rapidly than is implied by the current literature.

摘要

我们已经确定了大肠杆菌RNA上5'-核苷三磷酸的分布情况。这些基团代表RNA聚合酶启动转录时最初掺入的核苷三磷酸。据估计,至少15%与多核糖体相关的信使RNA带有三磷酸基团。这被解释为意味着对于大多数信使RNA的功能而言,去除三磷酸基团或信使RNA前导序列并非必要,但在多核糖体库中会发生大量的信使RNA加工过程。我们发现,以GTP起始的信使RNA与以ATP起始的信使RNA的比例约为2比1。由于先前的研究表明以G和A起始的RNA降解速率相同,且信使RNA起始位点的汇总显示偏好A,这个比值意味着对于以G起始的转录本存在显著的生理选择。我们还对其他组分中RNA的5'-末端基团进行了表征。发现少量与30S核糖体相关,推测存在于起始复合物中;此前尚未在原位检测到此类复合物。此外,得出的结论是,核糖体RNA前体的5'末端加工速度比当前文献所暗示的要快。