A novel antisense RNA regulates at transcriptional level the virulence gene icsA of Shigella flexneri

被引:60
|
作者
Giangrossi, Mara [2 ]
Prosseda, Gianni [1 ]
Tran, Chi Nhan [2 ]
Brandi, Anna [2 ]
Colonna, Bianca [1 ]
Falconi, Maurizio [2 ]
机构
[1] Univ Roma La Sapienza, Dept Cell & Dev Biol, Ist Pasteur Fdn Cenci Bolognetti, I-00185 Rome, Italy
[2] Univ Camerino, Mol Genet Lab, Dept Biol MCA, I-62032 Camerino, MC, Italy
关键词
SMALL NONCODING RNAS; IN-VIVO OLIGOMERIZATION; OUTER-MEMBRANE; MESSENGER-RNA; ESCHERICHIA-COLI; VIBRIO-CHOLERAE; VIRF PROMOTER; 6S RNA; H-NS; PROTEIN;
D O I
10.1093/nar/gkq025
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The virulence gene icsA of Shigella flexneri encodes an invasion protein crucial for host colonization by pathogenic bacteria. Within the intergenic region virA-icsA, we have discovered a new gene that encodes a non-translated antisense RNA (named RnaG), transcribed in cis on the complementary strand of icsA. In vitro transcription assays show that RnaG promotes premature termination of transcription of icsA mRNA. Transcriptional inhibition is also observed in vivo by monitoring the expression profile in Shigella by real-time polymerase chain reaction and when RnaG is provided in trans. Chemical and enzymatic probing of the leader region of icsA mRNA either free or bound to RnaG indicate that upon hetero-duplex formation an intrinsic terminator, leading to transcription block, is generated on the nascent icsA mRNA. Mutations in the hairpin structure of the proposed terminator impair the RnaG mediated-regulation of icsA transcription. This study represents the first evidence of transcriptional attenuation mechanism caused by a small RNA in Gram-negative bacteria. We also present data on the secondary structure of the antisense region of RnaG. In addition, alternatively silencing icsA and RnaG promoters, we find that transcription from the strong RnaG promoter reduces the activity of the weak convergent icsA promoter through the transcriptional interference regulation.
引用
收藏
页码:3362 / 3375
页数:14
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