J 2010

Srs2: the Odd-Job Man in DNA repair

MARINI PALOMEQUE, María Victoria a Lumír KREJČÍ

Základní údaje

Originální název

Srs2: the Odd-Job Man in DNA repair

Název česky

Srs2: Muž pro všechno v DNA opravě

Autoři

MARINI PALOMEQUE, María Victoria (858 Uruguay, domácí) a Lumír KREJČÍ (203 Česká republika, garant, domácí)

Vydání

DNA Repair, ELSEVIER, 2010, 1568-7864

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

10600 1.6 Biological sciences

Stát vydavatele

Nizozemské království

Utajení

není předmětem státního či obchodního tajemství

Impakt faktor

Impact factor: 4.293

Kód RIV

RIV/00216224:14310/10:00043104

Organizační jednotka

Přírodovědecká fakulta

UT WoS

000276016800008

Klíčová slova anglicky

DNA repair; DNA damage; replication; genomic instability

Příznaky

Mezinárodní význam, Recenzováno
Změněno: 19. 1. 2011 05:36, doc. Mgr. Lumír Krejčí, Ph.D.

Anotace

V originále

The genome is constantly threatened by various damaging agents and maintaining its integrity is crucial in all organisms. Several repair pathways have been implicated in the removal of different types of lesions from DNA. Among them, homologous recombination (HR) plays a key role in repair of double-strand breaks (DSBs). Although HR is a highly important repair mechanism, it has to be regulated to prevent it from interfering with other DNA repair pathways, generating toxic intermediates, or blocking the progression of the replication fork. Therefore, it is not surprising that cells have evolved mechanisms that counteract untimely HR events. In the yeast Saccharomyces cerevisiae, one of the pathways responsible for regulation of HR requires the action of the SRS2 gene product. Mutations in the SRS2 gene exhibit pleiotropic recombination phenotypes ranging from anti-recombinogenic in one aspect to pro-recombinogenic in another. In addition to its role in HR, Srs2 is also involved in other DNA metabolism processes, including post-replication repair (PRR), preservation of replication fork integrity, DNA-damage checkpoint responses, DNA triplet maintenance and non-homologous end joining (NHEJ). The aim of this review is to summarize the current knowledge about Srs2 and its effect on multiple DNA metabolic processes that generally affect genome stability. It would appear that Srs2 functions as an Odd-Job Man in these processes to make sure that the jobs proceed when and where they are needed.

Česky

The genome is constantly threatened by various damaging agents and maintaining its integrity is crucial in all organisms. Several repair pathways have been implicated in the removal of different types of lesions from DNA. Among them, homologous recombination (HR) plays a key role in repair of double-strand breaks (DSBs). Although HR is a highly important repair mechanism, it has to be regulated to prevent it from interfering with other DNA repair pathways, generating toxic intermediates, or blocking the progression of the replication fork. Therefore, it is not surprising that cells have evolved mechanisms that counteract untimely HR events. In the yeast Saccharomyces cerevisiae, one of the pathways responsible for regulation of HR requires the action of the SRS2 gene product. Mutations in the SRS2 gene exhibit pleiotropic recombination phenotypes ranging from anti-recombinogenic in one aspect to pro-recombinogenic in another. In addition to its role in HR, Srs2 is also involved in other DNA metabolism processes, including post-replication repair (PRR), preservation of replication fork integrity, DNA-damage checkpoint responses, DNA triplet maintenance and non-homologous end joining (NHEJ). The aim of this review is to summarize the current knowledge about Srs2 and its effect on multiple DNA metabolic processes that generally affect genome stability. It would appear that Srs2 functions as an Odd-Job Man in these processes to make sure that the jobs proceed when and where they are needed.

Návaznosti

GA301/09/1917, projekt VaV
Název: Štěpení replikačních-rekombinačních DNA meziproduktů a jejich úloha při nestabilitě genomu
Investor: Grantová agentura ČR, Štěpení replikačních-rekombinačních DNA meziproduktů a jejich úloha při nestabilitě genomu
GD203/09/H046, projekt VaV
Název: Biochemie na rozcestí mezi in silico a in vitro
Investor: Grantová agentura ČR, Biochemie na rozcestí mezi in silico a in vitro
LC06030, projekt VaV
Název: Biomolekulární centrum
Investor: Ministerstvo školství, mládeže a tělovýchovy ČR, Biomolekulární centrum
ME10048, projekt VaV
Název: Vliv post-translačních modifikací na DNA opravu a rekombinaci.
Investor: Ministerstvo školství, mládeže a tělovýchovy ČR, Vliv post-translačních modifikací na DNA opravu a rekombinaci., Program výzkumu a vývoje KONTAKT (ME)
MSM0021622413, záměr
Název: Proteiny v metabolismu a při interakci organismů s prostředím
Investor: Ministerstvo školství, mládeže a tělovýchovy ČR, Proteiny v metabolismu a při interakci organismů s prostředím