Literature DB >> 1853558

Nucleotide sequence of the bacteriophage P22 genes required for DNA packaging.

K Eppler1, E Wyckoff, J Goates, R Parr, S Casjens.   

Abstract

The mechanism of DNA packaging by dsDNA viruses is not well understood in any system. In bacteriophage P22 only five genes are required for successful condensation of DNA within the capsid. The products of three of these genes, the portal, scaffolding, and coat proteins, are structural components of the precursor particle, and two, the products of genes 2 and 3, are not. The scaffolding protein is lost from the structure during packaging, and only the portal and coat proteins are present in the mature virus particle. These five genes map in a contiguous cluster at the left end of the P22 genetic map. Three additional genes, 4, 10, and 26, are required for stabilizing of the condensed DNA within the capsid. In this report we present the nucleotide sequence of 7461 bp of P22 DNA that contains the five genes required for DNA condensation, as well as a nonessential open reading frame (ORF109), gene 4, and a portion of gene 10. N-terminal amino acid sequencing of the encoded proteins accurately located the translation starts of six genes in the sequence. Despite the fact that most of these proteins have striking analogs in the other dsDNA bacteriophage groups, which perform highly analogous functions, no amino acid sequence similarity between these analogous proteins has been found, indicating either that they diverged a very long time ago or that they are the products of spectacular convergent evolution.

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Year:  1991        PMID: 1853558     DOI: 10.1016/0042-6822(91)90981-g

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  48 in total

1.  Cloning and analysis of the capsid morphogenesis genes of Pseudomonas aeruginosa bacteriophage D3: another example of protein chain mail?

Authors:  Z A Gilakjan; A M Kropinski
Journal:  J Bacteriol       Date:  1999-12       Impact factor: 3.490

2.  Sequence of Shiga toxin 2 phage 933W from Escherichia coli O157:H7: Shiga toxin as a phage late-gene product.

Authors:  G Plunkett; D J Rose; T J Durfee; F R Blattner
Journal:  J Bacteriol       Date:  1999-03       Impact factor: 3.490

3.  GroEL binds a late folding intermediate of phage P22 coat protein.

Authors:  M D de Beus; S M Doyle; C M Teschke
Journal:  Cell Stress Chaperones       Date:  2000-07       Impact factor: 3.667

4.  The carboxy-terminal 14 amino acids of phage lambda N protein are dispensable for transcription antitermination.

Authors:  N C Franklin
Journal:  J Bacteriol       Date:  1992-12       Impact factor: 3.490

5.  The pKO2 linear plasmid prophage of Klebsiella oxytoca.

Authors:  Sherwood R Casjens; Eddie B Gilcrease; Wai Mun Huang; Kim L Bunny; Marisa L Pedulla; Michael E Ford; Jennifer M Houtz; Graham F Hatfull; Roger W Hendrix
Journal:  J Bacteriol       Date:  2004-03       Impact factor: 3.490

6.  Nucleotide sequence of the head assembly gene cluster of bacteriophage L and decoration protein characterization.

Authors:  Eddie B Gilcrease; Danella A Winn-Stapley; F Curtis Hewitt; Lisa Joss; Sherwood R Casjens
Journal:  J Bacteriol       Date:  2005-03       Impact factor: 3.490

7.  GroEL/S substrate specificity based on substrate unfolding propensity.

Authors:  Kristin N Parent; Carolyn M Teschke
Journal:  Cell Stress Chaperones       Date:  2007       Impact factor: 3.667

8.  Nucleotide sequence of the DNA packaging and capsid synthesis genes of bacteriophage P2.

Authors:  N A Linderoth; R Ziermann; E Haggård-Ljungquist; G E Christie; R Calendar
Journal:  Nucleic Acids Res       Date:  1991-12       Impact factor: 16.971

9.  The genome of epsilon15, a serotype-converting, Group E1 Salmonella enterica-specific bacteriophage.

Authors:  Andrew M Kropinski; Irina V Kovalyova; Stephen J Billington; Aaron N Patrick; Brent D Butts; Jared A Guichard; Trevor J Pitcher; Carly C Guthrie; Anya D Sydlaske; Lisa M Barnhill; Kyle A Havens; Kenneth R Day; Darrel R Falk; Michael R McConnell
Journal:  Virology       Date:  2007-09-07       Impact factor: 3.616

10.  Fluorescent amplified fragment length polymorphism analysis of Salmonella enterica serovar typhimurium reveals phage-type- specific markers and potential for microarray typing.

Authors:  Honghua Hu; Ruiting Lan; Peter R Reeves
Journal:  J Clin Microbiol       Date:  2002-09       Impact factor: 5.948

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