Literature DB >> 7597035

Precursor of C4 antisense RNA of bacteriophages P1 and P7 is a substrate for RNase P of Escherichia coli.

R K Hartmann1, J Heinrich, J Schlegl, H Schuster.   

Abstract

The C4 repressor of the temperate bacteriophages P1 and P7 inhibits antirepressor (Ant) synthesis and is essential for establishment and maintenance of lysogeny. C4 is an antisense RNA acting on a target, Ant mRNA, which is transcribed from the same promoter. The antisense-target RNA interaction requires processing of C4 RNA from a precursor RNA. Here we show that 5' maturation of C4 RNA in vivo depends on RNase P. In vitro, Escherichia coli RNase P and its catalytic RNA subunit (M1 RNA) can generate the mature 5' end of C4 RNA from P1 by a single endonucleolytic cut, whereas RNase P from the E. coli rnpA49 mutant, carrying a missense mutation in the RNase P protein subunit, is defective in the 5' maturation of C4 RNA. Primer extension analysis of RNA transcribed in vivo from a plasmid carrying the P1 c4 gene revealed that 5'-mature C4 RNA was the predominant species in rnpA+ bacteria, whereas virtually no mature C4 RNA was found in the temperature-sensitive rnpA49 strain at the restrictive temperature. Instead, C4 RNA molecules carrying up to five extra nucleotides beyond the 5' end accumulated. The same phenotype was observed in rnpA+ bacteria which harbored a plasmid carrying a P7 c4 mutant gene with a single C-->G base substitution in the structural homologue to the CCA 3' end of tRNAs. Implications of C4 RNA processing for the lysis/lysogeny decision process of bacteriophages P1 and P7 are discussed.

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Year:  1995        PMID: 7597035      PMCID: PMC41593          DOI: 10.1073/pnas.92.13.5822

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  25 in total

1.  Transcriptional control via translational repression by c4 antisense RNA of bacteriophages P1 and P7.

Authors:  A L Biere; M Citron; H Schuster
Journal:  Genes Dev       Date:  1992-12       Impact factor: 11.361

2.  The c4 repressor of bacteriophage P1 is a processed 77 base antisense RNA.

Authors:  M Citron; H Schuster
Journal:  Nucleic Acids Res       Date:  1992-06-25       Impact factor: 16.971

3.  The c4 repressors of bacteriophages P1 and P7 are antisense RNAs.

Authors:  M Citron; H Schuster
Journal:  Cell       Date:  1990-08-10       Impact factor: 41.582

4.  Reconstitution of enzymatic activity from fragments of M1 RNA.

Authors:  C Guerrier-Takada; S Altman
Journal:  Proc Natl Acad Sci U S A       Date:  1992-02-15       Impact factor: 11.205

5.  Determinants of Escherichia coli RNase P cleavage site selection: a detailed in vitro and in vivo analysis.

Authors:  S G Svärd; L A Kirsebom
Journal:  Nucleic Acids Res       Date:  1993-02-11       Impact factor: 16.971

6.  Organization of the immunity region immI of bacteriophage P1 and synthesis of the P1 antirepressor.

Authors:  A Heisig; H D Riedel; B Dobrinski; R Lurz; H Schuster
Journal:  J Mol Biol       Date:  1989-10-20       Impact factor: 5.469

Review 7.  Recent studies of ribonuclease P.

Authors:  S Altman; L Kirsebom; S Talbot
Journal:  FASEB J       Date:  1993-01       Impact factor: 5.191

8.  Differential evolution of substrates for an RNA enzyme in the presence and absence of its protein cofactor.

Authors:  F Liu; S Altman
Journal:  Cell       Date:  1994-07-01       Impact factor: 41.582

9.  Cleavage efficiencies of model substrates for ribonuclease P from Escherichia coli and Thermus thermophilus.

Authors:  J Schlegl; J P Fürste; R Bald; V A Erdmann; R K Hartmann
Journal:  Nucleic Acids Res       Date:  1992-11-25       Impact factor: 16.971

10.  Several regions of a tRNA precursor determine the Escherichia coli RNase P cleavage site.

Authors:  S G Svärd; L A Kirsebom
Journal:  J Mol Biol       Date:  1992-10-20       Impact factor: 5.469

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  36 in total

1.  Multiple binding modes of substrate to the catalytic RNA subunit of RNase P from Escherichia coli.

Authors:  D A Pomeranz Krummel; S Altman
Journal:  RNA       Date:  1999-08       Impact factor: 4.942

2.  UV cross-link mapping of the substrate-binding site of an RNase P ribozyme to a target mRNA sequence.

Authors:  A F Kilani; F Liu
Journal:  RNA       Date:  1999-09       Impact factor: 4.942

Review 3.  Eukaryotic ribonuclease P: a plurality of ribonucleoprotein enzymes.

Authors:  Shaohua Xiao; Felicia Scott; Carol A Fierke; David R Engelke
Journal:  Annu Rev Biochem       Date:  2001-11-09       Impact factor: 23.643

4.  Substrate binding and catalysis by ribonuclease P from cyanobacteria and Escherichia coli are affected differently by the 3' terminal CCA in tRNA precursors.

Authors:  A Pascual; A Vioque
Journal:  Proc Natl Acad Sci U S A       Date:  1999-06-08       Impact factor: 11.205

5.  Putative intermediary stages for the molecular evolution from a ribozyme to a catalytic RNP.

Authors:  Yoshiya Ikawa; Kentaro Tsuda; Shigeyoshi Matsumura; Shota Atsumi; Tan Inoue
Journal:  Nucleic Acids Res       Date:  2003-03-01       Impact factor: 16.971

Review 6.  Of proteins and RNA: the RNase P/MRP family.

Authors:  Olga Esakova; Andrey S Krasilnikov
Journal:  RNA       Date:  2010-07-13       Impact factor: 4.942

7.  Ribonuclease P: the evolution of an ancient RNA enzyme.

Authors:  Scott C Walker; David R Engelke
Journal:  Crit Rev Biochem Mol Biol       Date:  2006 Mar-Apr       Impact factor: 8.250

8.  Evidence that substrate-specific effects of C5 protein lead to uniformity in binding and catalysis by RNase P.

Authors:  Lei Sun; Frank E Campbell; Nathan H Zahler; Michael E Harris
Journal:  EMBO J       Date:  2006-08-24       Impact factor: 11.598

Review 9.  Inhibition of gene expression in human cells using RNase P-derived ribozymes and external guide sequences.

Authors:  Kihoon Kim; Fenyong Liu
Journal:  Biochim Biophys Acta       Date:  2007-09-29

10.  Genome of bacteriophage P1.

Authors:  Małgorzata B Łobocka; Debra J Rose; Guy Plunkett; Marek Rusin; Arkadiusz Samojedny; Hansjörg Lehnherr; Michael B Yarmolinsky; Frederick R Blattner
Journal:  J Bacteriol       Date:  2004-11       Impact factor: 3.490

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