Volume 178, Issue 1 pp. 123-128

Cloning of two cold shock genes, cspA and cspG, from the deep-sea psychrophilic bacterium Shewanella violacea strain DSS12

Shinsuke Fujii

Corresponding Author

Shinsuke Fujii

The DEEPSTAR Group, Japan Marine Science and Technology Center, 2-15 Natsushima-cho, Yokosuka 237-0061, Japan

*Corresponding author. Tel.: +81 (468) 67 3894; Fax: +81 (468) 66 6364, E-mail address: [email protected]Search for more papers by this author
Kaoru Nakasone

Kaoru Nakasone

The DEEPSTAR Group, Japan Marine Science and Technology Center, 2-15 Natsushima-cho, Yokosuka 237-0061, Japan

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Koki Horikoshi

Koki Horikoshi

The DEEPSTAR Group, Japan Marine Science and Technology Center, 2-15 Natsushima-cho, Yokosuka 237-0061, Japan

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First published: 17 January 2006
Citations: 4

Abstract

We cloned and characterized two cold shock inducible genes from the deep-sea psychrophilic bacterium Shewanella violacea strain DSS12. The cloned genes, designated cspA and cspG, encode proteins each consisting of 70 amino acid residues which show 62 and 67% sequence identity with Escherichia coli CspA and CspG, respectively. AT-rich UP elements were found immediately upstream of the promoter region and the cspA and cspG mRNA contained unusually long 5′ untranslated regions like that in the E. coli cspA, cspB, cspG and cspI genes. Following a temperature downshift to 4°C or −1°C, the levels of cspA and cspG mRNA increased and the level of expression of cspG was greater than that of cspA both before and after cold shock. These results suggest that CspA and CspG may function as RNA chaperones, the mRNAs encoded by these two genes may be regulated post-transcriptionally and they may function as regulators of other cold shock inducible genes like in E. coli.

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