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Three essential ribonucleases-RNase Y, J1, and III-control the abundance of a majority of Bacillus subtilis mRNAs.
Durand, Sylvain; Gilet, Laetitia; Bessières, Philippe; Nicolas, Pierre; Condon, Ciarán.
Afiliação
  • Durand S; CNRS UPR 9073, University Paris Diderot, Sorbonne Paris Cité, Institut de Biologie Physico-Chimique, Paris, France.
PLoS Genet ; 8(3): e1002520, 2012.
Article em En | MEDLINE | ID: mdl-22412379
ABSTRACT
Bacillus subtilis possesses three essential enzymes thought to be involved in mRNA decay to varying degrees, namely RNase Y, RNase J1, and RNase III. Using recently developed high-resolution tiling arrays, we examined the effect of depletion of each of these enzymes on RNA abundance over the whole genome. The data are consistent with a model in which the degradation of a significant number of transcripts is dependent on endonucleolytic cleavage by RNase Y, followed by degradation of the downstream fragment by the 5'-3' exoribonuclease RNase J1. However, many full-size transcripts also accumulate under conditions of RNase J1 insufficiency, compatible with a model whereby RNase J1 degrades transcripts either directly from the 5' end or very close to it. Although the abundance of a large number of transcripts was altered by depletion of RNase III, this appears to result primarily from indirect transcriptional effects. Lastly, RNase depletion led to the stabilization of many low-abundance potential regulatory RNAs, both in intergenic regions and in the antisense orientation to known transcripts.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Bacillus subtilis / RNA Mensageiro / Regulação Bacteriana da Expressão Gênica / Estabilidade de RNA / Ribonuclease III Idioma: En Revista: PLoS Genet Assunto da revista: GENETICA Ano de publicação: 2012 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Bacillus subtilis / RNA Mensageiro / Regulação Bacteriana da Expressão Gênica / Estabilidade de RNA / Ribonuclease III Idioma: En Revista: PLoS Genet Assunto da revista: GENETICA Ano de publicação: 2012 Tipo de documento: Article País de afiliação: França