Skip Navigation

This Article
Right arrow Print PDF (3418K)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (27)
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by LeBowitz, J. H.
Right arrow Articles by McMacken, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by LeBowitz, J. H.
Right arrow Articles by McMacken, R.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 1984, Vol. 12, No. 7 3069-3088
© 1984


MOLECULAR BIOLOGY

The bacteriophage {lambda} O and P protein initiators promote the replication of single-stranded DNA

Jonathan H. LeBowitz and Roger McMacken

Department of Biochemistry, School of Hygiene and Public Health, Johns Hopkins University 615 North Wolfe Street, Baltimore, MD 21205, USA

Received January 19, 1984. Accepted March 12, 1984.

A soluble enzyme system that specifically initiates {lambda}dy plasmid DNA replication at a bacteriophage {lambda} replication origin [Wold et al. (1982) Proc. Natl. Acad. Sci. USA 79, 6176–6180] is also capable of replicating the single–stranded circular chromosomes of phages M13 and øX174 to a duplex form. This chain initiation on single–stranded templates is novel in that it is absolutely dependent on the {lambda} O and P protein chromosomal initiators and on several Escherichia coli proteins that are known to function in the replication of the {lambda} chromosome in vivo, including the host dnaB, dnaG (primase), dnaJ and dnaK replication proteins. Strand initiation occurs at multiple sites following an O and P protein–dependent pre–priming step in which the DNA is converted into an activated nucleoprotein complex containing the bacterial dnaB protein. We propose a scheme for the initiation of DNA synthesis on single–stranded templates in this enzyme system that may be relevant to strand initiation events that occur during replication of phage {lambda} in vivo.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
M. Gonciarz-Swiatek, A. Wawrzynow, S.-J. Um, B. A. Learn, R. McMacken, W. L. Kelley, C. Georgopoulos, O. Sliekers, and M. Zylicz
Recognition, Targeting, and Hydrolysis of the lambda  O Replication Protein by the ClpP/ClpX Protease
J. Biol. Chem., May 14, 1999; 274(20): 13999 - 14005.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
K. M. Stephens and R. McMacken
Functional Properties of Replication Fork Assemblies Established by the Bacteriophage lambda  O and P Replication Proteins
J. Biol. Chem., November 7, 1997; 272(45): 28800 - 28813.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
B. A. Learn, S.-J. Um, L. Huang, and R. McMacken
Cryptic single-stranded-DNA binding activities of the phage lambda  P and Escherichia coli DnaC replication initiation proteins facilitate the transfer of E. coli DnaB helicase onto DNA
PNAS, February 18, 1997; 94(4): 1154 - 1159.
[Abstract] [Full Text] [PDF]


Home page
Genes Dev.Home page
J H LeBowitz, T Kobayashi, L Staudt, D Baltimore, and P A Sharp
Octamer-binding proteins from B or HeLa cells stimulate transcription of the immunoglobulin heavy-chain promoter in vitro.
Genes & Dev., October 1, 1988; 2(10): 1227 - 1237.
[Abstract] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.