Maes Alexandre, Gracia Céline, Innocenti Nicolas, Zhang Kaiyang, Aurell Erik, Hajnsdorf Eliane
CNRS UMR8261 (previously FRE3630) associated with University Paris Diderot, Sorbonne Paris Cité, Institut de Biologie Physico-Chimique, 13 rue P. et M. Curie, 75005 Paris, France.
Department of Computational Biology, KTH Royal Institute of Technology, AlbaNova University Center, Roslagstullsbacken 17, SE-10691 Stockholm, Sweden.
Nucleic Acids Res. 2017 Mar 17;45(5):2746-2756. doi: 10.1093/nar/gkw894.
Polyadenylation is thought to be involved in the degradation and quality control of bacterial RNAs but relatively few examples have been investigated. We used a combination of 5΄-tagRACE and RNA-seq to analyze the total RNA content from a wild-type strain and from a poly(A)polymerase deleted mutant. A total of 178 transcripts were either up- or down-regulated in the mutant when compared to the wild-type strain. Poly(A)polymerase up-regulates the expression of all genes related to the FliA regulon and several previously unknown transcripts, including numerous transporters. Notable down-regulation of genes in the expression of antigen 43 and components of the type 1 fimbriae was detected. The major consequence of the absence of poly(A)polymerase was the accumulation of numerous sRNAs, antisense transcripts, REP sequences and RNA fragments resulting from the processing of entire transcripts. A new algorithm to analyze the position and composition of post-transcriptional modifications based on the sequence of unencoded 3΄-ends, was developed to identify polyadenylated molecules. Overall our results shed new light on the broad spectrum of action of polyadenylation on gene expression and demonstrate the importance of poly(A) dependent degradation to remove structured RNA fragments.
聚腺苷酸化被认为与细菌RNA的降解和质量控制有关,但相对较少的例子得到研究。我们结合使用5΄-tagRACE和RNA测序来分析野生型菌株和聚(A)聚合酶缺失突变体的总RNA含量。与野生型菌株相比,突变体中共有178个转录本上调或下调。聚(A)聚合酶上调了所有与FliA调控子相关的基因以及一些先前未知的转录本的表达,包括许多转运蛋白。检测到抗原43表达和1型菌毛成分中的基因显著下调。聚(A)聚合酶缺失的主要后果是大量sRNA、反义转录本、REP序列和由完整转录本加工产生的RNA片段的积累。我们开发了一种基于未编码3΄-末端序列分析转录后修饰位置和组成的新算法,以识别聚腺苷酸化分子。总体而言,我们的结果为聚腺苷酸化在基因表达上的广泛作用机制提供了新的见解,并证明了依赖聚(A)的降解对于去除结构化RNA片段的重要性。