Hajnsdorf E, Braun F, Haugel-Nielsen J, Le Derout J, Régnier P
Institut de Biologie Physico-Chimique, Paris, France.
Biochimie. 1996;78(6):416-24. doi: 10.1016/0300-9084(96)84748-1.
The degradation process of the rpsO mRNA is one of the best characterised in E coli. Two independent degradation pathways have been identified. The first one is initiated by an RNase E endonucleolytic cleavage which allows access to the transcript by polynucleotide phosphorylase and RNase II. Cleavage by RNase E gives rise to an rpsO message lacking the stabilising hairpin of the primary transcript; this truncated mRNA is then degraded exonucleolytically from its 3' terminus. This pathway might be coupled to the translation of the message. The second pathway allows degradation of polyadenylated rpsO mRNA independently of RNase II, PNPase and RNase E. The ribonucleases responsible for degradation of poly(A) mRNAs under these conditions are not known. Poly(A) tails have been proposed to facilitate the degradation of structured RNA by polynucleotide phosphorylase. In contrast, we believe that removal of poly(A) by RNase II stabilises the rpsO mRNA harbouring a 3' hairpin. In addition to these two pathways, we have identified endonucleolytic cleavages which occur only in strains deficient for both RNase E and RNase III suggesting that these two endonucleases protect the 5' leader of the mRNA from the attack of unidentified ribonuclease(s). Looping of the rpsO mRNA might explain how RNase E bound at the 5' end can cleave at a site located just upstream the hairpin of the transcription terminator.
rpsO mRNA的降解过程是大肠杆菌中特征最为明确的过程之一。已鉴定出两条独立的降解途径。第一条途径由核糖核酸酶E(RNase E)的内切核酸酶切割引发,这使得多核苷酸磷酸化酶和核糖核酸酶II能够接触到转录本。RNase E的切割产生了一种缺乏初级转录本稳定发夹结构的rpsO信息;然后这种截短的mRNA从其3'末端开始进行外切核酸酶降解。这条途径可能与该信息的翻译相偶联。第二条途径允许多聚腺苷酸化的rpsO mRNA独立于RNase II、多核苷酸磷酸化酶(PNPase)和RNase E进行降解。在这些条件下负责降解多聚(A)mRNA的核糖核酸酶尚不清楚。有人提出多聚(A)尾巴有助于多核苷酸磷酸化酶对结构化RNA的降解。相反,我们认为RNase II去除多聚(A)会使带有3'发夹结构的rpsO mRNA稳定。除了这两条途径,我们还鉴定出了仅在RNase E和RNase III均缺陷的菌株中发生的内切核酸酶切割,这表明这两种内切核酸酶保护mRNA的5'前导序列免受未鉴定的核糖核酸酶的攻击。rpsO mRNA的环化可能解释了结合在5'末端的RNase E如何能在转录终止子发夹结构上游的位点进行切割。