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Sequence‐selective interactions with RNA by CspB, CspC and CspE, members of the CspA family of Escherichia coli
Author(s) -
Phadtare Sangita,
Inouye Masayori
Publication year - 1999
Publication title -
molecular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.857
H-Index - 247
eISSN - 1365-2958
pISSN - 0950-382X
DOI - 10.1046/j.1365-2958.1999.01541.x
Subject(s) - cold shock domain , biology , rna , escherichia coli , riboswitch , binding site , rna binding protein , dna , gene , biochemistry , non coding rna
The CspA family of Escherichia coli comprises nine homologous proteins, CspA to CspI. CspA, the major cold shock protein, binds RNA with low sequence specificity and low binding affinity. This is considered to be important for its proposed function as an RNA chaperone to prevent the formation of secondary structures in RNA molecules, thus facilitating translation at low temperature. The cellular functions of other Csp proteins are yet to be fully elucidated, and their sequence specific binding capabilities have not been identified. As a step towards identification of the target genes of Csp proteins, we investigated the RNA binding specificities of CspB, CspC and CspE by an in vitro selection approach (SELEX). In the present study, we show that these proteins are able to bind preferentially to specific RNA/single‐stranded DNA sequences. The consensus sequences for CspB, CspC and CspE are U/T stretches, AGGGAGGGA and AU/AT‐rich regions, especially AAAUUU, respectively. CspE and CspB have K d values in the range 0.23–0.9 × 10 −6 M, while CspC has 10‐fold lower binding affinity. Consistent with our recent findings of transcriptional regulation of cspA by CspE, we have identified a motif identical to the CspE consensus. This motif is the putative CspE‐mediated transcription pause recognition site in a 5′‐untranslated region of the cspA mRNA.