SraL sRNA interaction regulates the terminator by preventing premature transcription termination of rho mRNA
SraL sRNA interaction regulates the terminator by preventing premature transcription termination of rho mRNA
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SraL sRNA 相互作用通过防止 rho mRNA 过早转录终止来调节终止子
DOI:
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发表时间:
2019
影响因子:
11.1
通讯作者:
C. Arraiano
中科院分区:
文献类型:
--
作者:
I. J. Silva;Susana Barahona;Alex Eyraud;David Lalaouna;N. Figueroa;É. Massé;C. Arraiano
Significance Rho is an essential protein that promotes transcription termination at specific regions of the genome. Its activity is important not only at the end of genes, but also within leader regions where it has regulatory functions. This protein was shown to be involved in the regulation of rho mRNA promoting its premature transcription termination. In this study, we included an additional player in the complex pathway of regulation of this protein. Using in vivo and in vitro experiments, the small noncoding RNA SraL was shown to directly interact with a specific region in the 5′-UTR of rho mRNA protecting this transcript against the action of its own protein Rho. Transcription termination is a critical step in the control of gene expression. One of the major termination mechanisms is mediated by Rho factor that dissociates the complex mRNA-DNA-RNA polymerase upon binding with RNA polymerase. Rho promotes termination at the end of operons, but it can also terminate transcription within leader regions, performing regulatory functions and avoiding pervasive transcription. Transcription of rho is autoregulated through a Rho-dependent attenuation in the leader region of the transcript. In this study, we have included an additional player in this pathway. By performing MS2-affinity purification coupled with RNA sequencing (MAPS), rho transcript was shown to directly interact with the small noncoding RNA SraL. Using bioinformatic in vivo and in vitro experimental analyses, SraL was shown to base pair with the 5′-UTR of rho mRNA upregulating its expression in several growth conditions. This base pairing was shown to prevent the action of Rho over its own message. Moreover, the results obtained indicate that both ProQ and Hfq are associated with this regulation. We propose a model that contemplates the action of Salmonella SraL sRNA in the protection of rho mRNA from premature transcription termination by Rho. Note that since the interaction region between both RNAs corresponds to a very-well-conserved sequence, it is plausible to admit that this regulation also occurs in other enterobacteria.
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影响因子:
10.5
作者:
Wassarman, KM;Repoila, F;Gottesman, S
通讯作者:
Gottesman, S
影响因子:
30.3
作者:
Kroeger, Carsten;Colgan, Aoife;Hinton, Jay C. D.
通讯作者:
Hinton, Jay C. D.
影响因子:
5.4
作者:
Kavita, Kumari;de Mets, Francois;Gottesman, Susan
通讯作者:
Gottesman, Susan
影响因子:
7.2
作者:
Gottesman, Susan;Storz, Gisela
通讯作者:
Storz, Gisela
DOI:
10.1073/pnas.95.21.12462
发表时间:
1998-10-13
影响因子:
11.1
作者:
Majdalani, N;Cunning, C;Gottesman, S
通讯作者:
Gottesman, S