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Processing of Bacillus subtilis small cytoplasmic RNA: evidence for an additional endonuclease cleavage site

机译:枯草芽孢杆菌小细胞质RNA的加工:一个额外的核酸内切酶裂解位点的证据

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摘要

Small cytoplasmic RNA (scRNA) of Bacillus subtilis is the RNA component of the signal recognition particle. scRNA is transcribed as a 354-nt precursor, which is processed to the mature 271-nt scRNA. Previous work demonstrated the involvement of the RNase III-like endoribonuclease, Bs-RNase III, in scRNA processing. Bs-RNase III was found to cleave precursor scRNA at two sites (the 5' and 3' cleavage sites) located on opposite sides of the stem of a large stem-loop structure, yielding a 275-nt RNA, which was then trimmed by a 3' exoribonuclease to the mature scRNA. Here we show that Bs-RNase III cleaves primarily at the 5' cleavage site and inefficiently at the 3' site. RNase J1 is responsible for much of the cleavage that releases scRNA from downstream sequences. The subsequent exonucleolytic processing is carried out largely by RNase PH.
机译:枯草芽孢杆菌的小细胞质RNA(scRNA)是信号识别颗粒的RNA成分。 scRNA被转录为354 nt的前体,然后被加工成成熟的271 nt的scRNA。先前的工作证明了RNase III样核糖核酸内切酶Bs-RNase III参与scRNA加工。发现Bs-RNase III在大茎环结构茎的相对侧的两个位点(5'和3'裂解位点)裂解前体scRNA,产生275 nt的RNA,然后对其进行修剪成熟scRNA的3'外切核糖核酸酶。在这里,我们显示Bs-RNase III主要在5'裂解位点裂解,而在3'裂解效率低下。 RNase J1负责从下游序列释放scRNA的大部分切割。随后的核酸外切加工主要由RNase PH进行。

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