DNA decay and limited Rad53 activation after liquid holding of UV-treated nucleotide excision repair deficient S. cerevisiae cells.
DNA Repair (Amst)
; 3(12): 1591-9, 2004 Dec 02.
Article
em En
| MEDLINE
| ID: mdl-15474420
ABSTRACT
The DNA damage checkpoint is a surveillance mechanism activated by DNA lesions and devoted to the maintenance of genome stability. It is considered as a signal transduction cascade, involving a sensing step, the activation of a set of protein kinases and the transmission and amplification of the damage signal through several phosphorylation events. In budding yeast many players of this pathway have been identified. Recent work showed that G1 and G2 checkpoint activation in response to UV irradiation requires prior recognition and processing of UV lesions by nucleotide excision repair (NER) factors that likely recruit checkpoint proteins near the damage. However, another report suggested that NER was not required for checkpoint function. Since the functional relationship between repair mechanisms and checkpoint activation is a very important issue in the field, we analyzed, under different experimental conditions, whether lesion processing by NER is required for checkpoint activation. We found that DNA damage checkpoint can be triggered in an NER-independent manner only if cells are subjected to liquid holding after UV treatment. This incubation causes a time-dependent breakage of DNA strands in NER-deficient cells and leads to partial activation of the checkpoint kinase. The analysis of the genetic requirements for this alternative activation pathway suggest that it requires Mec1 and the Rad17 complex and that the observed DNA breaks are likely to be due to spontaneous decay of damaged DNA.
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Base de dados:
MEDLINE
Assunto principal:
Saccharomyces cerevisiae
/
Raios Ultravioleta
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Dano ao DNA
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Proteínas Serina-Treonina Quinases
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Proteínas de Ciclo Celular
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Proteínas de Saccharomyces cerevisiae
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Reparo do DNA
Idioma:
En
Ano de publicação:
2004
Tipo de documento:
Article