Growth-rate-dependent regulation of 6-phosphogluconate dehydrogenase level mediated by an anti-Shine-Dalgarno sequence located within the Escherichia coli gnd structural gene.
- 1 February 1989
- journal article
- research article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 86 (4) , 1138-1142
- https://doi.org/10.1073/pnas.86.4.1138
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 severalsites 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.Keywords
This publication has 24 references indexed in Scilit:
- A unique mechanism regulating gene expression: translational inhibition by a complementary RNA transcript (micRNA).Proceedings of the National Academy of Sciences, 1984
- DNA sequence of the Escherichia coli gene, gnd, for 6-phosphogluconate dehydrogenaseGene, 1984
- Translational control of IS10 transpositionCell, 1983
- A role for mRNA secondary structure in the control of translation initiationNature, 1982
- Optimal computer folding of large RNA sequences using thermodynamics and auxiliary informationNucleic Acids Research, 1981
- Posttranscriptional modification of mRNA conformation: Mechanism that regulates erythromycin-induced resistanceProceedings of the National Academy of Sciences, 1980
- Growth-rate-dependent alteration of 6-phosphogluconate dehydrogenase and glucose 6-phosphate dehydrogenase levels in Escherichia coli K-12Journal of Bacteriology, 1979
- Improved Estimation of Secondary Structure in Ribonucleic AcidsNature New Biology, 1973
- Prophage lambda at unusual chromosomal locations: I. Location of the secondary attachment sites and the properties of the lysogensJournal of Molecular Biology, 1972
- Growth rate of polypeptide chains as a function of the cell growth rate in a mutant of Escherichia coli 15Journal of Molecular Biology, 1971