Literature DB >> 14504214

Genetics of cosQ, the DNA-packaging termination site of phage lambda: local suppressors and methylation effects.

Douglas J Wieczorek1, Michael Feiss.   

Abstract

The cos site of the bacteriophage lambda chromosome contains the sites required for DNA processing and packaging during virion assembly. cos is composed of three subsites, cosQ, cosN, and cosB. cosQ is required for the termination of chromosome packaging. Previous studies have shown cosQ mutations to be suppressed in three ways: by a local suppressor within cosQ; by an increase in the length of the lambda chromosome; and by missense mutations affecting the prohead's portal protein, gpB. In the first study reported here, revertants of a set of cosQ mutants were screened for suppressors, and cis-acting suppressors of cosQ mutations were studied; these included second-site cosQ point mutations, base-pair insertions within cosQ, and an additional genome-lengthening suppressor. The 7-bp-long cosQ, with the sequence 5'-GGGTCCT-3', coincides exactly with the recognition site for the EcoO109I restriction/methylation system, which has the consensus sequence 5'-PuGGNCCPy-3'. In a second study, EcoO109I methylation was found to strongly interfere with the residual cosQ function of leaky cosQ mutants. cis-acting suppressors that overcome methylation-associated defects, including a methylation-dependent suppressor, were also isolated. Models of cosQ suppression are presented.

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Mesh:

Year:  2003        PMID: 14504214      PMCID: PMC1462750     

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


  21 in total

1.  Studies on the cleavage of bacteriophage lambda DNA with EcoRI Restriction endonuclease.

Authors:  M Thomas; R W Davis
Journal:  J Mol Biol       Date:  1975-01-25       Impact factor: 5.469

2.  Characterization and overproduction of EcoO109I methyltransferase.

Authors:  K Kita; J Tsuda; R Nishigaki
Journal:  Biosci Biotechnol Biochem       Date:  2001-11       Impact factor: 2.043

Review 3.  Bacteriophage lambda DNA: the beginning of the end.

Authors:  A Becker; H Murialdo
Journal:  J Bacteriol       Date:  1990-06       Impact factor: 3.490

4.  DNA curvature in native and modified EcoRI recognition sites and possible influence upon the endonuclease cleavage reaction.

Authors:  S Diekmann; L W McLaughlin
Journal:  J Mol Biol       Date:  1988-08-20       Impact factor: 5.469

5.  Processing of the bacteriophage P1 packaging site (pac) is regulated by adenine methylation.

Authors:  N Sternberg; J N Coulby
Journal:  Gene       Date:  1988-12-25       Impact factor: 3.688

6.  Bacteriophage lambda derivatives carrying two copies of the cohesive end site.

Authors:  S W Emmons
Journal:  J Mol Biol       Date:  1974-03-15       Impact factor: 5.469

7.  Bacteriophage P4: a satellite virus depending on a helper such as prophage P2.

Authors:  E W Six; C A Klug
Journal:  Virology       Date:  1973-02       Impact factor: 3.616

8.  Restriction endonuclease EcoO109 from Escherichia coli H709c with heptanucleotide recognition site 5'-PuG/GNCCPy.

Authors:  K Mise; K Nakajima
Journal:  Gene       Date:  1985       Impact factor: 3.688

9.  Alterations of the portal protein, gpB, of bacteriophage lambda suppress mutations in cosQ, the site required for termination of DNA packaging.

Authors:  Douglas J Wieczorek; Lisa Didion; Michael Feiss
Journal:  Genetics       Date:  2002-05       Impact factor: 4.562

10.  A dominant (mutD5) and a recessive (dnaQ49) mutator of Escherichia coli.

Authors:  M Maruyama; T Horiuchi; H Maki; M Sekiguchi
Journal:  J Mol Biol       Date:  1983-07-15       Impact factor: 5.469

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