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枯草芽孢杆菌小细胞质RNA的转录与加工

Transcription and processing of Bacillus subtilis small cytoplasmic RNA.

作者信息

Struck J C, Hartmann R K, Toschka H Y, Erdmann V A

机构信息

Freie Universität Berlin, Institut für Biochemie.

出版信息

Mol Gen Genet. 1989 Feb;215(3):478-82. doi: 10.1007/BF00427046.

Abstract

The 271 nucleotides long scRNA (small cytoplasmic RNA) from Bacillus subtilis is structurally related to the Escherichia coli 4.5 S RNA (114 nucleotides), an essential molecule supposed to be involved in protein biosynthesis, but it possesses an additional moiety completely missing in the E. coli 4.5 S RNA. Both RNAs share a conserved hairpin with the eukaryotic 7SL RNAs, which mediate protein translocation as part of the signal recognition particle (SRP). We have cloned and sequenced the entire scRNA gene region from B. subtilis and have studied transcription and processing of the scRNA in B. subtilis by nuclease S1 mapping. This analysis revealed the scRNA gene to constitute a monofunctional transcription unit, expressed from a single promoter to a rho-independent terminator, yielding a precursor which extends the mature scRNA by approximately 40 nucleotides at both ends. Processing of the scRNA apparently involves only two endonucleolytic cuts and occurs first at the 5' end.

摘要

来自枯草芽孢杆菌的271个核苷酸长的小细胞质RNA(scRNA)在结构上与大肠杆菌的4.5S RNA(114个核苷酸)相关,后者是一种被认为参与蛋白质生物合成的必需分子,但它拥有一个在大肠杆菌4.5S RNA中完全缺失的额外部分。这两种RNA都与真核生物的7SL RNA共享一个保守的发夹结构,7SL RNA作为信号识别颗粒(SRP)的一部分介导蛋白质转运。我们已经克隆并测序了枯草芽孢杆菌的整个scRNA基因区域,并通过核酸酶S1图谱分析研究了枯草芽孢杆菌中scRNA的转录和加工过程。该分析表明,scRNA基因构成一个单功能转录单元,从单个启动子转录至一个不依赖于ρ因子的终止子,产生一个前体,该前体在成熟scRNA的两端各延伸约40个核苷酸。scRNA的加工显然仅涉及两次内切核酸酶切割,且首先发生在5'端。

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