NEJ1 controls non-homologous end joining in Saccharomyces cerevisiae

Citation
M. Valencia et al., NEJ1 controls non-homologous end joining in Saccharomyces cerevisiae, NATURE, 414(6864), 2001, pp. 666-669
Citations number
29
Categorie Soggetti
Multidisciplinary,Multidisciplinary,Multidisciplinary
Journal title
NATURE
ISSN journal
00280836 → ACNP
Volume
414
Issue
6864
Year of publication
2001
Pages
666 - 669
Database
ISI
SICI code
0028-0836(200112)414:6864<666:NCNEJI>2.0.ZU;2-Z
Abstract
Broken DNA ends are rejoined by non-homologous end-joining (NHEJ) pathways requiring the Ku proteins (Ku70, Ku80), DNA ligase IV and its associated pr otein Lif1/Xrcc4 (ref. 1). In mammalian meiotic cells, Ku protein levels ar e much lower than in somatic cells, apparently reducing the capacity of mei otic cells to carry out NHEJ and thereby promoting homologous recombination (2). In Saccharomyces cerevisiae, NHEJ is also downregulated in meiosis-com petent MATa/MAT alpha diploid cells in comparison with diploids or haploids expressing only MATa or MAT alpha (3,4). Diploids expressing both MATa and MAT alpha show enhanced mitotic homologous recombination(4). Here we repor t that mating-type-dependent regulation of NHEJ in budding yeast is caused in part by transcriptional repression of both LIF1 and the gene NEJ1 (YLR26 5C)-identified from microarray screening of messenger RNAs. Deleting NEJ1 r educes NHEJ 100-fold in MATa or MAT alpha haploids. Constitutive expression of NEJ1, but not expression of LIF1, restores NHEJ in MATa/MAT alpha cells . Nej1 regulates the subcellular distribution of Lif1. A green fluorescent protein (GFP)-Lif1 fusion protein accumulates in the nucleus in cells expre ssing NEJ1 but is largely cytoplasmic when NEJ1 is repressed.