Identification of two DNA helicases UvrD and DinG as suppressors for lethality caused by mutant cspA mRNAs.

ABSTRACT: CspA is a major cold shock-inducible protein (70 aa), and its major role in the cold shock response was shown to be as an RNA chaperone destabilizing secondary structure of mRNAs at low temperature. Previously, we showed that the overexpression of mutant cspA containing premature non-sense codons at various positions led to stalled ribosomes on mutant cspA transcripts, ultimately leading to cell death. This lethality is primarily due to the highly translatable cspA 5'-UTR that recruits most of the ribosomes from other mRNAs, which are then stalled at the abnormal stop codon. This was called the 'LACE' effect. We show here that non-sense mutation even at the 67th position as well as substitutions of aromatic amino acid residues present on the RNA-binding surface of CspA protein to alanine c

SUBMITTER: Hwang J 

PROVIDER: S-EPMC3480728 | biostudies-literature | 2012

REPOSITORIES: biostudies-literature