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聚腺苷酸化会使大肠杆菌的rpsO信使核糖核酸不稳定。

Polyadenylylation destabilizes the rpsO mRNA of Escherichia coli.

作者信息

Hajnsdorf E, Braun F, Haugel-Nielsen J, Régnier P

机构信息

Institut de Biologie Physico-Chimique, Paris, France.

出版信息

Proc Natl Acad Sci U S A. 1995 Apr 25;92(9):3973-7. doi: 10.1073/pnas.92.9.3973.

Abstract

The rpsO mRNA, encoding ribosomal protein S15, is only partly stabilized when the three ribonucleases implicated in its degradation--RNase E, polynucleotide phosphorylase, and RNase II--are inactivated. In the strain deficient for RNase E and 3'-to-5' exoribonucleases, degradation of this mRNA is correlated with the appearance of posttranscriptionally elongated molecules. We report that these elongated mRNAs harbor poly(A) tails, most of which are fused downstream of the 3'-terminal hairpin at the site where transcription terminates. Poly(A) tails are shorter in strains containing 3'-to-5' exoribonucleases. Inactivation of poly(A) polymerase I (pcnB) prevents polyadenylylation and stabilizes the rpsO mRNA if RNase E is inactive. In contrast polyadenylylation does not significantly modify the stability of rpsO mRNA undergoing RNase E-mediated degradation.

摘要

编码核糖体蛋白S15的rpsO mRNA,当参与其降解的三种核糖核酸酶(核糖核酸酶E、多核苷酸磷酸化酶和核糖核酸酶II)失活时,只是部分地得到稳定。在缺乏核糖核酸酶E和3'至5'外切核糖核酸酶的菌株中,这种mRNA的降解与转录后延长分子的出现相关。我们报告这些延长的mRNA带有聚腺苷酸尾巴,其中大多数在转录终止位点的3'末端发夹下游融合。在含有3'至5'外切核糖核酸酶的菌株中,聚腺苷酸尾巴较短。如果核糖核酸酶E无活性,聚腺苷酸聚合酶I(pcnB)的失活会阻止聚腺苷酸化并稳定rpsO mRNA。相比之下,聚腺苷酸化不会显著改变经历核糖核酸酶E介导降解的rpsO mRNA的稳定性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f14c/42084/ce9f03f180f5/pnas01493-0351-a.jpg

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