Eukaryotic TLS polymerases

TLS polymerases are able to replicate damaged DNA (called translesion DNA synthesis, TLS). Their presence prevents cell death as a result of violating the integrity of the genome. In vitro, they are mutator, but in vivo are recruited by specific types of DNA damage and usually replicate them in a co...

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Main Authors: Przemysław Tomczyk, Ewelina Synowiec, Daniel Wysokiński, Katarzyna Woźniak
Format: Article
Language:English
Published: Index Copernicus International S.A. 2016-05-01
Series:Postępy Higieny i Medycyny Doświadczalnej
Subjects:
Online Access:http://phmd.pl/gicid/01.3001.0009.6832
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spelling doaj-480fadddae094007a5eaec5213deef612020-11-24T23:56:03ZengIndex Copernicus International S.A.Postępy Higieny i Medycyny Doświadczalnej0032-54491732-26932016-05-017052253310.5604/01.3001.0009.683201.3001.0009.6832Eukaryotic TLS polymerasesPrzemysław Tomczyk0Ewelina Synowiec1Daniel Wysokiński2Katarzyna Woźniak3Katedra Genetyki Molekularnej, Wydział Biologii i Ochrony Środowiska, Uniwersytet ŁódzkiKatedra Genetyki Molekularnej, Wydział Biologii i Ochrony Środowiska, Uniwersytet ŁódzkiKatedra Genetyki Molekularnej, Wydział Biologii i Ochrony Środowiska, Uniwersytet ŁódzkiKatedra Genetyki Molekularnej, Wydział Biologii i Ochrony Środowiska, Uniwersytet ŁódzkiTLS polymerases are able to replicate damaged DNA (called translesion DNA synthesis, TLS). Their presence prevents cell death as a result of violating the integrity of the genome. In vitro, they are mutator, but in vivo are recruited by specific types of DNA damage and usually replicate them in a correct manner. The best-known TLS polymerases belong to the Y family, such as Rev1, κ, η, ι, and polymerase ζ from the B family. There are two mechanisms of TLS polymerases action: polymerase-switching model and the gap-filling model. Selection of the mechanism primarily depends on the phase of the cell cycle. The regulation of these polymerases may take place at the transcriptional level and at level of recruitment to the sites of DNA damage. In the latter case post-translational modification of proteins - ubiquitination and sumoylation, and protein-protein interactions are crucial. http://phmd.pl/gicid/01.3001.0009.6832DNA polymerasesDNA DamagereplicationPCNApolimerazy DNAuszkodzenia DNA
collection DOAJ
language English
format Article
sources DOAJ
author Przemysław Tomczyk
Ewelina Synowiec
Daniel Wysokiński
Katarzyna Woźniak
spellingShingle Przemysław Tomczyk
Ewelina Synowiec
Daniel Wysokiński
Katarzyna Woźniak
Eukaryotic TLS polymerases
Postępy Higieny i Medycyny Doświadczalnej
DNA polymerases
DNA Damage
replication
PCNA
polimerazy DNA
uszkodzenia DNA
author_facet Przemysław Tomczyk
Ewelina Synowiec
Daniel Wysokiński
Katarzyna Woźniak
author_sort Przemysław Tomczyk
title Eukaryotic TLS polymerases
title_short Eukaryotic TLS polymerases
title_full Eukaryotic TLS polymerases
title_fullStr Eukaryotic TLS polymerases
title_full_unstemmed Eukaryotic TLS polymerases
title_sort eukaryotic tls polymerases
publisher Index Copernicus International S.A.
series Postępy Higieny i Medycyny Doświadczalnej
issn 0032-5449
1732-2693
publishDate 2016-05-01
description TLS polymerases are able to replicate damaged DNA (called translesion DNA synthesis, TLS). Their presence prevents cell death as a result of violating the integrity of the genome. In vitro, they are mutator, but in vivo are recruited by specific types of DNA damage and usually replicate them in a correct manner. The best-known TLS polymerases belong to the Y family, such as Rev1, κ, η, ι, and polymerase ζ from the B family. There are two mechanisms of TLS polymerases action: polymerase-switching model and the gap-filling model. Selection of the mechanism primarily depends on the phase of the cell cycle. The regulation of these polymerases may take place at the transcriptional level and at level of recruitment to the sites of DNA damage. In the latter case post-translational modification of proteins - ubiquitination and sumoylation, and protein-protein interactions are crucial.
topic DNA polymerases
DNA Damage
replication
PCNA
polimerazy DNA
uszkodzenia DNA
url http://phmd.pl/gicid/01.3001.0009.6832
work_keys_str_mv AT przemysławtomczyk eukaryotictlspolymerases
AT ewelinasynowiec eukaryotictlspolymerases
AT danielwysokinski eukaryotictlspolymerases
AT katarzynawozniak eukaryotictlspolymerases
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