Literature DB >> 3005594

Processive action of terminase during sequential packaging of bacteriophage lambda chromosomes.

M Feiss, J Sippy, G Miller.   

Abstract

Bacteriophage lambda chromosomes are packaged in a polarized, sequential fashion from a multimeric DNA substrate. Mature chromosomes are generated when terminase introduces staggered nicks in the cohesive end sites (cos sites) bounding a chromosome. Packaging is polarized, to the initial and terminal cos sites for packaging a chromosome can be defined. To initiate packaging, terminase binds to cos at cosB, and subsequently cuts at cosN. To terminate packaging of a chromosome, a functional cosB is not required at the terminal cos. To explain this finding, it was proposed earlier that terminase scans for the terminal cosN, rather than any subsequent cosB, during packaging. In the work described here we performed helper packaging experiments to see whether processive action of terminase occurs during sequential packaging of lambda chromosomes. The helper packaging experiments involve trilysogens; strains carrying three prophages in tandem. Infection by a hetero-immune helper phage results in packaging of the repressed prophage chromosomes, since the prophage structure is analogous to the normal DNA substrate. Two chromosomes can be packaged from between the three cos sites of the prophages of a trilysogen. Both chromosomes are packaged even when the central cos is cosB-. Our interpretation of these data is that terminase is brought to the central cos by packaging; following cleavage of the central cos, the terminase remains bound to the distal chromosome; and terminase acts to begin packaging of the distal chromosome. The frequency at which terminase reads across the central cos to initiate packaging of the distal chromosome is in the range from 0.3 to 0.5 in our experiments. Reading across cos was found not to be greatly dependent on the state of cosB, indicating that cosB binding is only needed for packaging the first chromosome in a packaging series. A multilysogen was constructed in which the initial cos was cos+ and the distal cos sites were all cosB-. The initial and downstream chromosomes were found to be packaged. This result indicates that terminase that is brought to the central cos by packaging is not only able to initiate packaging of a downstream chromosome, but can also scan and terminate packaging of the downstream chromosome. A model is presented in which processive action of terminase is the basis for sequential packaging of lambda chromosomes.

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Year:  1985        PMID: 3005594     DOI: 10.1016/0022-2836(85)90395-x

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  13 in total

1.  Analysis of a mutation affecting the specificity domain for prohead binding of the bacteriophage lambda terminase.

Authors:  J Sippy; M Feiss
Journal:  J Bacteriol       Date:  1992-02       Impact factor: 3.490

2.  Further tests of a recombination model in which chi removes the RecD subunit from the RecBCD enzyme of Escherichia coli.

Authors:  F W Stahl; L C Thomason; I Siddiqi; M M Stahl
Journal:  Genetics       Date:  1990-11       Impact factor: 4.562

Review 3.  Little lambda, who made thee?

Authors:  Max E Gottesman; Robert A Weisberg
Journal:  Microbiol Mol Biol Rev       Date:  2004-12       Impact factor: 11.056

4.  Mutations in Nu1, the gene encoding the small subunit of bacteriophage lambda terminase, suppress the postcleavage DNA packaging defect of cosB mutations.

Authors:  Z H Cai; Y Hwang; D Cue; C Catalano; M Feiss
Journal:  J Bacteriol       Date:  1997-04       Impact factor: 3.490

5.  Defining cosQ, the site required for termination of bacteriophage lambda DNA packaging.

Authors:  D J Wieczorek; M Feiss
Journal:  Genetics       Date:  2001-06       Impact factor: 4.562

6.  A point mutation in the Nul gene of bacteriophage lambda facilitates phage growth in Escherichia coli with himA and gyrB mutations.

Authors:  A E Granston; D M Alessi; L J Eades; D I Friedman
Journal:  Mol Gen Genet       Date:  1988-04

Review 7.  Recombinational repair of DNA damage in Escherichia coli and bacteriophage lambda.

Authors:  A Kuzminov
Journal:  Microbiol Mol Biol Rev       Date:  1999-12       Impact factor: 11.056

8.  Genetic evidence that recognition of cosQ, the signal for termination of phage lambda DNA packaging, depends on the extent of head filling.

Authors:  D Cue; M Feiss
Journal:  Genetics       Date:  1997-09       Impact factor: 4.562

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 site required for termination of packaging of the phage lambda chromosome.

Authors:  D Cue; M Feiss
Journal:  Proc Natl Acad Sci U S A       Date:  1993-10-15       Impact factor: 11.205

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