Literature DB >> 6096564

A functional domain of bacteriophage lambda terminase for prohead binding.

S Frackman, D A Siegele, M Feiss.   

Abstract

Terminase is a multifunctional protein complex involved in DNA packaging during bacteriophage lambda assembly. Terminase is made of gpNul and gpA, the products of the phage lambda Nu1 and A genes. Early during DNA packaging terminase binds to lambda DNA to form a complex called complex I. Terminase is required for the binding of proheads by complex I to form a DNA: terminase: prohead complex known as complex II. Terminase remains associated with the DNA during encapsidation. The other known role for terminase in packaging is the production of staggered nicks in the DNA thereby generating the cohesive ends. Lambdoid phage 21 has cohesive ends identical to those of lambda. The head genes of lambda and 21 show partial sequence homology and are analogous in structure, function and position. The terminases of lambda and 21 are not interchangeable. At least two actions of terminase are involved in this specificity: (1) DNA binding; (2) prohead binding. The 1 and 2 genes at the left end of the 21 chromosome were identified as coding for the 21 terminase. gp1 and gp2 are analogous to gpNu1 and gpA, respectively. We have isolated a phage, lambda-21 hybrid 33, which is the product of a crossover between lambda and 21 within the terminase genes. Lambda-21 hybrid 33 DNA and terminase have phage 21 packaging specificity, as determined by complementation and helper packaging studies. The terminase of lambda-21 hybrid 33 requires lambda proheads for packaging. We have determined the position at which the crossover between lambda DNA and 21 DNA occurred to produce the hybrid phage. Lambda-21 hybrid 33 carries the phage 21 1 gene and a hybrid phage 2/A gene. Sequencing of lambda-21 hybrid 33 DNA shows that it encodes a protein that is homologous at the carboxy terminus with the 38 amino acids of the carboxy terminus of lambda gpA; the remainder of the protein is homologous to gp2. The results of these studies define a specificity domain for prohead binding at the carboxy terminus of gpA.

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Year:  1984        PMID: 6096564     DOI: 10.1016/s0022-2836(84)80005-4

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


  21 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

3.  Isolation and characterization of mutations in the bacteriophage lambda terminase genes.

Authors:  A Davidson; P Yau; H Murialdo; M Gold
Journal:  J Bacteriol       Date:  1991-08       Impact factor: 3.490

4.  Mutations that extend the specificity of the endonuclease activity of lambda terminase.

Authors:  J S Arens; Q Hang; Y Hwang; B Tuma; S Max; M Feiss
Journal:  J Bacteriol       Date:  1999-01       Impact factor: 3.490

5.  Demonstration of cotranscription and 1-methyl-3-nitroso-nitroguanidine induction of a 30-gene operon of Borrelia burgdorferi: evidence that the 32-kilobase circular plasmids are prophages.

Authors:  Hongming Zhang; Richard T Marconi
Journal:  J Bacteriol       Date:  2005-12       Impact factor: 3.490

Review 6.  The DNA-packaging nanomotor of tailed bacteriophages.

Authors:  Sherwood R Casjens
Journal:  Nat Rev Microbiol       Date:  2011-08-12       Impact factor: 60.633

7.  Domains for protein-protein interactions at the N and C termini of the large subunit of bacteriophage lambda terminase.

Authors:  W F Wu; S Christiansen; M Feiss
Journal:  Genetics       Date:  1988-07       Impact factor: 4.562

8.  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

9.  The bacteriophage lambda cohesive end site: isolation of spacing/substitution mutations that result in dependence on Escherichia coli integration host factor.

Authors:  G Miller; M Feiss
Journal:  Mol Gen Genet       Date:  1988-04

10.  On the clustered exchanges of the RecBCD pathway operating on phage lambda.

Authors:  F W Stahl; C E Shurvinton; L C Thomason; S Hill; M M Stahl
Journal:  Genetics       Date:  1995-03       Impact factor: 4.562

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