» Articles » PMID: 2521618

Retroregulation of the Bacteriophage Lambda Int Gene: Limited Secondary Degradation of the RNase III-processed Transcript

Overview
Journal J Bacteriol
Specialty Microbiology
Date 1989 Jan 1
PMID 2521618
Citations 9
Authors
Affiliations
Soon will be listed here.
Abstract

Expression of the int gene of bacteriophage lambda from two promoters, pI and pL, is differentially regulated through RNA processing. Efficient Int protein synthesis from the pL RNA is inhibited by the action of sib, a cis-acting retroregulator downstream from the int gene. We have used mapping procedures with nuclease S1 to study the pL transcripts produced in vivo after phage lambda infection. We have found an RNase III-dependent processing site within the Int coding sequence, 387 nucleotides upstream from the site of the primary cleavage by RNase III at Sib. This secondary processing site is located at the most stable region of secondary structure in the sib int region, as predicted by computer analysis. We suggest that RNase III cleavage at the Sib site allows processive exonucleolytic degradation of the RNA to proceed to a region of secondary structure within the Int coding sequence, which protects the upstream region of the transcript from further degradation.

Citing Articles

Study of the role of Mg in dsRNA processing mechanism by bacterial RNase III through QM/MM simulations.

Drusin S, Rasia R, Moreno D J Biol Inorg Chem. 2019; 25(1):89-98.

PMID: 31754801 DOI: 10.1007/s00775-019-01741-7.


RNA Sequencing Identifies New RNase III Cleavage Sites in and Reveals Increased Regulation of mRNA.

Gordon G, Cameron J, Pfleger B mBio. 2017; 8(2).

PMID: 28351917 PMC: 5371410. DOI: 10.1128/mBio.00128-17.


Identification of endoribonuclease specific cleavage positions reveals novel targets of RNase III in Streptococcus pyogenes.

Le Rhun A, Lecrivain A, Reimegard J, Proux-Wera E, Broglia L, Della Beffa C Nucleic Acids Res. 2017; 45(5):2329-2340.

PMID: 28082390 PMC: 5389636. DOI: 10.1093/nar/gkw1316.


Overexpression of an mRNA dependent on rare codons inhibits protein synthesis and cell growth.

Zahn K J Bacteriol. 1996; 178(10):2926-33.

PMID: 8631683 PMC: 178030. DOI: 10.1128/jb.178.10.2926-2933.1996.


Autoregulation of RNase III operon by mRNA processing.

Bardwell J, Regnier P, Chen S, Nakamura Y, GRUNBERG-MANAGO M, Court D EMBO J. 1989; 8(11):3401-7.

PMID: 2583104 PMC: 401487. DOI: 10.1002/j.1460-2075.1989.tb08504.x.


References
1.
Salser W, GESTELAND R, BOLLE A . In vitro synthesis of bacteriophage lysozyme. Nature. 1967; 215(5101):588-91. DOI: 10.1038/215588a0. View

2.
Summers W . A simple method for extraction of RNA from E. coli utilizing diethyl pyrocarbonate. Anal Biochem. 1970; 33(2):459-63. DOI: 10.1016/0003-2697(70)90316-7. View

3.
Kinscherf T, Apirion D . Polynucleotide phosphorylase can participate in decay of mRNA in Escherichia coli in the absence of ribonuclease II. Mol Gen Genet. 1975; 139(4):357-62. DOI: 10.1007/BF00267975. View

4.
Berk A, Sharp P . Spliced early mRNAs of simian virus 40. Proc Natl Acad Sci U S A. 1978; 75(3):1274-8. PMC: 411453. DOI: 10.1073/pnas.75.3.1274. View

5.
Guarneros G, Galindo J . The regulation of integrative recombination by the b2 region and the cII gene of bacteriophage lambda. Virology. 1979; 95(1):119-26. DOI: 10.1016/0042-6822(79)90406-9. View