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Characterization of an unusual bipolar helicase encoded by bacteriophage T5

Bacteriophage T5 has a 120 kb double-stranded linear DNA genome encoding most of the genes required for its own replication. This lytic bacteriophage has a burst size of ∼500 new phage particles per infected cell, demonstrating that it is able to turn each infected bacterium into a highly efficient...

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Autores principales: Wong, Io Nam, Sayers, Jon R., Sanders, Cyril M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3632103/
https://www.ncbi.nlm.nih.gov/pubmed/23435232
http://dx.doi.org/10.1093/nar/gkt105
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author Wong, Io Nam
Sayers, Jon R.
Sanders, Cyril M.
author_facet Wong, Io Nam
Sayers, Jon R.
Sanders, Cyril M.
author_sort Wong, Io Nam
collection PubMed
description Bacteriophage T5 has a 120 kb double-stranded linear DNA genome encoding most of the genes required for its own replication. This lytic bacteriophage has a burst size of ∼500 new phage particles per infected cell, demonstrating that it is able to turn each infected bacterium into a highly efficient DNA manufacturing machine. To begin to understand DNA replication in this prodigious bacteriophage, we have characterized a putative helicase encoded by gene D2. We show that bacteriophage T5 D2 protein is the first viral helicase to be described with bipolar DNA unwinding activities that require the same core catalytic residues for unwinding in either direction. However, unwinding of partially single- and double-stranded DNA test substrates in the 3′–5′ direction is more robust and can be distinguished from the 5′–3′ activity by a number of features including helicase complex stability, salt sensitivity and the length of single-stranded DNA overhang required for initiation of helicase action. The presence of D2 in an early gene cluster, the identification of a putative helix-turn-helix DNA-binding motif outside the helicase core and homology with known eukaryotic and prokaryotic replication initiators suggest an involvement for this unusual helicase in DNA replication initiation.
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spelling pubmed-36321032013-04-22 Characterization of an unusual bipolar helicase encoded by bacteriophage T5 Wong, Io Nam Sayers, Jon R. Sanders, Cyril M. Nucleic Acids Res Nucleic Acid Enzymes Bacteriophage T5 has a 120 kb double-stranded linear DNA genome encoding most of the genes required for its own replication. This lytic bacteriophage has a burst size of ∼500 new phage particles per infected cell, demonstrating that it is able to turn each infected bacterium into a highly efficient DNA manufacturing machine. To begin to understand DNA replication in this prodigious bacteriophage, we have characterized a putative helicase encoded by gene D2. We show that bacteriophage T5 D2 protein is the first viral helicase to be described with bipolar DNA unwinding activities that require the same core catalytic residues for unwinding in either direction. However, unwinding of partially single- and double-stranded DNA test substrates in the 3′–5′ direction is more robust and can be distinguished from the 5′–3′ activity by a number of features including helicase complex stability, salt sensitivity and the length of single-stranded DNA overhang required for initiation of helicase action. The presence of D2 in an early gene cluster, the identification of a putative helix-turn-helix DNA-binding motif outside the helicase core and homology with known eukaryotic and prokaryotic replication initiators suggest an involvement for this unusual helicase in DNA replication initiation. Oxford University Press 2013-04 2013-02-21 /pmc/articles/PMC3632103/ /pubmed/23435232 http://dx.doi.org/10.1093/nar/gkt105 Text en © The Author(s) 2013. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Nucleic Acid Enzymes
Wong, Io Nam
Sayers, Jon R.
Sanders, Cyril M.
Characterization of an unusual bipolar helicase encoded by bacteriophage T5
title Characterization of an unusual bipolar helicase encoded by bacteriophage T5
title_full Characterization of an unusual bipolar helicase encoded by bacteriophage T5
title_fullStr Characterization of an unusual bipolar helicase encoded by bacteriophage T5
title_full_unstemmed Characterization of an unusual bipolar helicase encoded by bacteriophage T5
title_short Characterization of an unusual bipolar helicase encoded by bacteriophage T5
title_sort characterization of an unusual bipolar helicase encoded by bacteriophage t5
topic Nucleic Acid Enzymes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3632103/
https://www.ncbi.nlm.nih.gov/pubmed/23435232
http://dx.doi.org/10.1093/nar/gkt105
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