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PMID: 9044269 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Promoter-independent cold-shock induction of cspA and its derepression at 37 degrees C by mRNA stabilization.

Molecular microbiology ·Vol. 23 ·No. 2 ·1997-01-00 ·Pages 355-64

Fang L, Jiang W, Bae W, Inouye M

Abstract

The gene for CspA, the major cold-shock protein of Escherichia coli is known to be dramatically induced upon temperature downshift. Here, we report that three-base substitutions around the Shine-Dalgarno sequence in the 159-base 5'-untranslated region of the cspA mRNA stabilizes the mRNA 150-fold, resulting in constitutive expression of cspA at 37 degrees C. This stabilization was found to be at least partially due to resistance against RNase E degradation. The cold-shock induction of cspA was also achieved by exchanging its promoter with the non-cold-shock Ipp promoter. The results presented indicate that the cspA gene is efficiently transcribed even at 37 degrees C. However, the translation of the cspA mRNA is blocked because of its extreme instability at 37 degrees C. The presented results also demonstrate that the cspA gene is constitutively transcribed at all temperatures; however, its expression at 37 degrees C is prevented by destabilizing its mRNA.

MeSH Terms
Bacterial Proteins/genetics Cold Temperature DNA Mutational Analysis DNA Primers Electrophoresis, Gel, Two-Dimensional Escherichia coli/genetics Hot Temperature Molecular Structure Oligonucleotides Polymerase Chain Reaction RNA, Messenger/chemistry,genetics
Chemicals
Bacterial Proteins DNA Primers Oligonucleotides RNA, Messenger cold shock protein CS7.4, Bacteria
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Fang L
Department of Biochemistry, Robert Wood Johnson Medical School, Piscataway, New Jersey 08854, USA.
Jiang W
Bae W
Inouye M
Article Info
Journal
Molecular microbiology
Abbr.
Mol Microbiol
ISSN
0950-382X
Published
1997-01-00
Pages
355-64
Language
English
Region
England
NLM ID
8712028
Subset
IM
Grants
NIGMS NIH HHS · GM19043 · United States
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