recA gene expression in a streptomycete is mediated by the unusual C-terminus of RecA protein

Streptomyces RecA proteins are characterized by a conserved, positively charged extension of unknown function appended at their C-termini. To investigate the function of this element, we introduced the Streptomyces rimosus recA gene and its mutant form encoding the protein with a C-terminal deletion...

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Bibliographic Details
Published inFEMS microbiology letters Vol. 248; no. 1; pp. 119 - 124
Main Authors Ahel, Ivan, Mikoc, Andreja, Gamulin, Vera
Format Journal Article
LanguageEnglish
Published Oxford, UK Elsevier B.V 01.07.2005
Blackwell Publishing Ltd
Blackwell
Oxford University Press
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Summary:Streptomyces RecA proteins are characterized by a conserved, positively charged extension of unknown function appended at their C-termini. To investigate the function of this element, we introduced the Streptomyces rimosus recA gene and its mutant form encoding the protein with a C-terminal deletion into S. rimosus. Both transcript and protein levels were dramatically increased in the strain expressing the truncated gene compared to the strain bearing the wild-type recA, indicating involvement of the characteristic C-terminal extension in regulating the recA expression in Streptomyces. Considering that RecA acts as a major regulator of DNA damage response in bacteria, this mode of regulation is expected to have broader implications and significance that outreaches our current understanding of RecA autoregulation.
Bibliography:Edited by J.A. Gil
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ISSN:0378-1097
1574-6968
DOI:10.1016/j.femsle.2005.05.030