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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Published in | FEMS microbiology letters Vol. 248; no. 1; pp. 119 - 124 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Oxford, UK
Elsevier B.V
01.07.2005
Blackwell Publishing Ltd Blackwell Oxford University Press |
Subjects | |
Online Access | Get full text |
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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. |
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Bibliography: | Edited by J.A. Gil ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 0378-1097 1574-6968 |
DOI: | 10.1016/j.femsle.2005.05.030 |