Post-transcriptional regulation of <italic>NifA</italic> expression by Hfq and RNase E complex in <italic>Rhizobium leguminosarum</italic> bv. <italic>viciae</italic>
Author(s) -
Yinghua Zhang,
Guofan Hong
Publication year - 2009
Publication title -
acta biochimica et biophysica sinica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.771
H-Index - 57
eISSN - 1745-7270
pISSN - 1672-9145
DOI - 10.1093/abbs/gmp060
Subject(s) - rnase p , ribosomal binding site , start codon , rhizobium leguminosarum , transcriptional regulation , gene , gene expression , biology , messenger rna , microbiology and biotechnology , rna , chemistry , ribosome , genetics , bacteria , rhizobiaceae , symbiosis
NifA is the general transcriptional activator of nitrogen fixation genes in diazotrophic bacteria. In Rhizobium leguminosarum bv. viciae strain 8401/pRL1JI, the NifA gene is part of a gene cluster (fixABCXNifAB). In this study, results showed that in R. leguminosarum bv.viciae 8401/pRL1JI, host factor required (Hfq), and RNase E were involved in the post-transcriptional regulation of NifA expression. It was found that Hfq-dependent RNase E cleavage of NifA mRNA was essential for NifA translation. The cleavage site is located at 32 nucleotides upstream of the NifA translational start codon. A possible explanation based on predicted RNA secondary structure of the NifA 5'-untranslated region was that the cleavage made ribosome-binding sites accessible for translation.
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