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DNA Polymerase e - More Than a Polymerase

This paper presents a comprehensive review of the structure and function of DNA polymerase e. Together with DNA polymerases a and d, this enzyme replicates the nuclear DNA in the eukaryotic cell. During this process, DNA polymerase a lays down RNA-DNA primers that are utilized by DNA polymerases d a...

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Autores principales: Pospiech, Helmut, Syväoja, Juhani E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: TheScientificWorldJOURNAL 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974877/
https://www.ncbi.nlm.nih.gov/pubmed/12806123
http://dx.doi.org/10.1100/tsw.2003.08
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author Pospiech, Helmut
Syväoja, Juhani E.
author_facet Pospiech, Helmut
Syväoja, Juhani E.
author_sort Pospiech, Helmut
collection PubMed
description This paper presents a comprehensive review of the structure and function of DNA polymerase e. Together with DNA polymerases a and d, this enzyme replicates the nuclear DNA in the eukaryotic cell. During this process, DNA polymerase a lays down RNA-DNA primers that are utilized by DNA polymerases d and e for the bulk DNA synthesis. Attempts have been made to assign these two enzymes specifically to the synthesis of the leading and the lagging strand. Alternatively, the two DNA polymerases may be needed to replicate distinct regions depending on chromatin structure. Surprisingly, the essential function of DNA polymerase e does not depend on its catalytic activity, but resides in the nonenzymatic carboxy-terminal domain. This domain not only mediates the interaction of the catalytic subunit with the three smaller regulatory subunits, but also links the replication machinery to the S phase checkpoint. In addition to its role in DNA replication, DNA polymerase e fulfils roles in the DNA synthesis step of nucleotide excision and base excision repair, and has been implicated in recombinational processes in the cell.
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spelling pubmed-59748772018-06-10 DNA Polymerase e - More Than a Polymerase Pospiech, Helmut Syväoja, Juhani E. ScientificWorldJournal Review Article This paper presents a comprehensive review of the structure and function of DNA polymerase e. Together with DNA polymerases a and d, this enzyme replicates the nuclear DNA in the eukaryotic cell. During this process, DNA polymerase a lays down RNA-DNA primers that are utilized by DNA polymerases d and e for the bulk DNA synthesis. Attempts have been made to assign these two enzymes specifically to the synthesis of the leading and the lagging strand. Alternatively, the two DNA polymerases may be needed to replicate distinct regions depending on chromatin structure. Surprisingly, the essential function of DNA polymerase e does not depend on its catalytic activity, but resides in the nonenzymatic carboxy-terminal domain. This domain not only mediates the interaction of the catalytic subunit with the three smaller regulatory subunits, but also links the replication machinery to the S phase checkpoint. In addition to its role in DNA replication, DNA polymerase e fulfils roles in the DNA synthesis step of nucleotide excision and base excision repair, and has been implicated in recombinational processes in the cell. TheScientificWorldJOURNAL 2003-03-24 /pmc/articles/PMC5974877/ /pubmed/12806123 http://dx.doi.org/10.1100/tsw.2003.08 Text en Copyright © 2003 Helmut Pospiech and Juhani E. Syväoja. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Pospiech, Helmut
Syväoja, Juhani E.
DNA Polymerase e - More Than a Polymerase
title DNA Polymerase e - More Than a Polymerase
title_full DNA Polymerase e - More Than a Polymerase
title_fullStr DNA Polymerase e - More Than a Polymerase
title_full_unstemmed DNA Polymerase e - More Than a Polymerase
title_short DNA Polymerase e - More Than a Polymerase
title_sort dna polymerase e - more than a polymerase
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974877/
https://www.ncbi.nlm.nih.gov/pubmed/12806123
http://dx.doi.org/10.1100/tsw.2003.08
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