Literature DB >> 2668290

Altered expression of the bacteriophage T4 gene 41 (primase-helicase) in an Escherichia coli rho mutant.

D M Hinton1.   

Abstract

Bacteriophage T4 gene 41 protein is an essential replication protein, part of the primase-helicase required for lagging strand DNA synthesis. In a T4+ infection, 41 RNA is first expressed as a polycistronic transcript attached to the upstream RNA of genes uvsX (recombination protein) and 40 (stimulates head formation (Hinton, D. M. (1989) J. Biol. Chem. 264, 14432-14439). As infection proceeds, less of the upstream RNA extends into gene 41 due to an RNA 3' end, approximately equal to 60 bases downstream of uvsX. DNA sequence analysis of this region positions this end within gene 40, immediately after a GC-rich hairpin. This end probably arises from host factor-dependent transcription termination or RNA processing since it is observed in RNA expressed by a uvsX-40-41 plasmid in vivo, but is not seen after in vitro transcription with purified Escherichia coli RNA polymerase. The E. coli transcription termination (rho) mutant rho026 has been characterized as a rho mutation whose terminating activity is not effectively overcome by phage lambda antitermination (Das, A., Gottesman, M. E., Wardwell, J., Trisler, P., and Gottesman, S. (1983) Proc. Natl. Acad. Sci. U. S. A. 80, 5530-5534). During a T4+ abortive infection of rho026, the levels of some phage proteins, including 41, are depressed; a T4 phage mutant in goF gives wild type protein patterns in rho026 (Stitt, B. L., and Mosig, G. (1989) J. Bacteriol., in press). The RNA analyses presented here demonstrate that the severalfold decrease in 41 protein in rho026 is accompanied by a similar decrease in 41 RNA. There is both a general reduction in polycistronic uvsX-40-41 RNA and a 2-2.5-fold increase in the proportion of uvsX RNA ending at the 3' end. Infection of rho026 by T4 goF1 returns the relative amount of RNA reading into 41 versus that stopped to near a wild type level. These results suggest that host rho and the T4 goF are involved in the expression of T4 41 RNA.

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Year:  1989        PMID: 2668290

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  5 in total

1.  Identification of a family of bacteriophage T4 genes encoding proteins similar to those present in group I introns of fungi and phage.

Authors:  M Sharma; R L Ellis; D M Hinton
Journal:  Proc Natl Acad Sci U S A       Date:  1992-07-15       Impact factor: 11.205

Review 2.  Bacteriophage T4 genome.

Authors:  Eric S Miller; Elizabeth Kutter; Gisela Mosig; Fumio Arisaka; Takashi Kunisawa; Wolfgang Rüger
Journal:  Microbiol Mol Biol Rev       Date:  2003-03       Impact factor: 11.056

3.  Sequence and characterization of the bacteriophage T4 comC alpha gene product, a possible transcription antitermination factor.

Authors:  B Sanson; M Uzan
Journal:  J Bacteriol       Date:  1992-10       Impact factor: 3.490

4.  Effect of Escherichia coli nusG function on lambda N-mediated transcription antitermination.

Authors:  S L Sullivan; D F Ward; M E Gottesman
Journal:  J Bacteriol       Date:  1992-02       Impact factor: 3.490

5.  A late exclusion of bacteriophage T4 can be suppressed by Escherichia coli GroEL or Rho.

Authors:  C H Linder; K Carlson; F Albertioni; J Söderström; C Påhlson
Journal:  Genetics       Date:  1994-07       Impact factor: 4.562

  5 in total

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