Abstract
Previous work has shown that in Escherichia coli K-12 growth-rate-dependent regulation of expression of 6-phosphogluconate dehydrogenase, encoded by the gnd gene, occurs at the posttranscriptional level and is mediated by a negative control element that lies deep in the coding sequence, somewhere between codons 48 and 118. Deletion analysis of a growth-rate-regulated gnd-lacZ translational fusion showed that the element is the segment of gnd mRNA between codons 67 and 78 that is complementary to an extensive portion of the gnd ribosome-binding site, including its Shine-Dalgarno sequence. The boundaries of the element were further defined by the cloning of a synthetic "internal complementary sequence." The core internal complementary sequence element effected growth-rate-dependent regulation when placed at several sites between codon 40 and codon 69, but it severely reduced gene expression when moved to codon 13. The effect on regulation of single and double mutations introduced into the element by site-directed mutagenesis correlated with the ability of the respective mRNAs to fold into secondary structures that sequester the ribosome-binding site. Thus the gnd gene's internal regulatory element appears to function as a cis-acting antisense RNA.
MeSH Terms
Base Sequence
Chromosome Deletion
DNA, Recombinant/metabolism
Escherichia coli/enzymology,genetics,growth & development
Genes
Genes, Bacterial
Genes, Regulator
Molecular Sequence Data
Nucleic Acid Conformation
Phosphogluconate Dehydrogenase/genetics
Plasmids
RNA/genetics
RNA, Antisense
RNA, Messenger/antagonists & inhibitors,genetics
Restriction Mapping
Chemicals
DNA, Recombinant
RNA, Antisense
RNA, Messenger
RNA
Phosphogluconate Dehydrogenase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Carter-Muenchau P
Department of Biological Sciences, University of Maryland, Baltimore County 21228.
Wolf R E
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