NEJ1 controls non-homologous end joining in Saccharomyces cerevisiae

Broken DNA ends are rejoined by non-homologous end-joining (NHEJ) pathways requiring the Ku proteins (Ku70, Ku80), DNA ligase IV and its associated protein Lif1/Xrcc4 (ref. 1 ). In mammalian meiotic cells, Ku protein levels are much lower than in somatic cells, apparently reducing the capacity of me...

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Veröffentlicht in:Nature (London) 2001-12, Vol.414 (6864), p.666-669
Hauptverfasser: Valencia, Maria, Bentele, Marc, Vaze, Moreshwar B., Herrmann, Gernot, Kraus, Eliayhu, Lee, Sang Eun, Schär, Primo, Haber, James E.
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Sprache:eng
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Zusammenfassung:Broken DNA ends are rejoined by non-homologous end-joining (NHEJ) pathways requiring the Ku proteins (Ku70, Ku80), DNA ligase IV and its associated protein Lif1/Xrcc4 (ref. 1 ). In mammalian meiotic cells, Ku protein levels are much lower than in somatic cells, apparently reducing the capacity of meiotic cells to carry out NHEJ and thereby promoting homologous recombination 2 . In Saccharomyces cerevisiae , NHEJ is also downregulated in meiosis-competent MAT a/ MAT α diploid cells in comparison with diploids or haploids expressing only MAT a or MAT α 3 , 4 . Diploids expressing both MAT a and MAT α show enhanced mitotic homologous recombination 4 . Here we report that mating-type-dependent regulation of NHEJ in budding yeast is caused in part by transcriptional repression of both LIF1 and the gene NEJ1 (YLR265C)—identified from microarray screening of messenger RNAs. Deleting NEJ1 reduces NHEJ 100-fold in MAT a or MAT α haploids. Constitutive expression of NEJ1 , but not expression of LIF1 , restores NHEJ in MAT a/ MAT α cells. Nej1 regulates the subcellular distribution of Lif1. A green fluorescent protein (GFP)–Lif1 fusion protein accumulates in the nucleus in cells expressing NEJ1 but is largely cytoplasmic when NEJ1 is repressed.
ISSN:0028-0836
1476-4687
DOI:10.1038/414666a