Open AccessSequence analysis and transcriptional regulation of theEscherichia coil grpEgene, encoding a heat shock protein
Author(s) -
Barbara Lipińska,
J. King,
D. D. Áng,
Costa Georgopoulos
Publication year - 1988
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/16.15.7545
Subject(s) - biology , gene , microbiology and biotechnology , transcription (linguistics) , heat shock protein , escherichia coli , peptide sequence , hspa12a , promoter , messenger rna , consensus sequence , genetics , heat shock , gene expression , philosophy , linguistics
We have sequenced the Escherichia coli grpE gene and shown that it encodes a 197-amino acid residue protein of 21,668-Mr. The predicted N-terminal amino acid sequence, as well as the overall amino acid composition agree well with that of the purified protein. From Northern analysis, we have shown that transcription of the grpE gene is under heat shock regulation, i.e., there is a rapid and transient increase in the rate of synthesis of grpE mRNA upon a shift-up in temperature. Forty-six bases upstream of the structural gene is a sequence closely related to the consensus heat shock promoter identified by Cowing et al. [Proc. Natl. Acad. Sci. U.S.A, 82, 2679-2683]. We have shown by S1 mapping and RNA sequencing that this is indeed the promoter for the grpE mRNA. It appears that all discernable transcription initiates only from this promoter, even under non-heat shock conditions.