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 |
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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. |
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ISSN: | 0028-0836 1476-4687 |
DOI: | 10.1038/414666a |