Crossing over is regulated to occur at least once per each pair of homologous chromosomes during meiotic prophase to ensure proper segregation of chromosomes at the first meiotic division. In a mer3 deletion mutant of Saccharomyces cerevisiae, crossing over is decreased, and the distribution of the crossovers that occur is random. The predicted Mer3 protein contains seven motifs characteristic of the DExH box type of DNA/RNA helicases. The mer3G166D and the mer3K167A mutation, amino acid substitutions of conserved residues in a putative nucleotide-binding domain of the helicase motifs caused a defect in the transition of meiosis-specific double-strand breaks to later intermediates, decreased crossing over, and reduced crossover interference. The purified Mer3 protein was found to have DNA helicase activity. This helicase activity was reduced by the mer3GD mutation to <1% of the wild-type activity, even though binding of the mutant protein to single- and double-strand DNA was unaffected. The mer3KA mutation eliminated the ATPase activity of the wild-type protein. These results demonstrate that Mer3 is a DNA helicase that functions in meiotic crossing over.
机构:Yale Univ, Howard Hughes Med Inst, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA
Agarwal, S
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Roeder, GS
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Yale Univ, Howard Hughes Med Inst, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USAYale Univ, Howard Hughes Med Inst, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA
机构:Stanford Univ, Howard Hughes Med Inst, Sch Med, Dept Biochem, Stanford, CA 94305 USA
Chu, S
;
DeRisi, J
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机构:Stanford Univ, Howard Hughes Med Inst, Sch Med, Dept Biochem, Stanford, CA 94305 USA
DeRisi, J
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Eisen, M
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机构:Stanford Univ, Howard Hughes Med Inst, Sch Med, Dept Biochem, Stanford, CA 94305 USA
Eisen, M
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Mulholland, J
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机构:Stanford Univ, Howard Hughes Med Inst, Sch Med, Dept Biochem, Stanford, CA 94305 USA
Mulholland, J
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Botstein, D
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机构:Stanford Univ, Howard Hughes Med Inst, Sch Med, Dept Biochem, Stanford, CA 94305 USA
Botstein, D
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Brown, PO
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Stanford Univ, Howard Hughes Med Inst, Sch Med, Dept Biochem, Stanford, CA 94305 USAStanford Univ, Howard Hughes Med Inst, Sch Med, Dept Biochem, Stanford, CA 94305 USA
Brown, PO
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Herskowitz, I
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机构:Stanford Univ, Howard Hughes Med Inst, Sch Med, Dept Biochem, Stanford, CA 94305 USA
机构:Yale Univ, Howard Hughes Med Inst, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA
Agarwal, S
;
Roeder, GS
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Yale Univ, Howard Hughes Med Inst, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USAYale Univ, Howard Hughes Med Inst, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA
机构:Stanford Univ, Howard Hughes Med Inst, Sch Med, Dept Biochem, Stanford, CA 94305 USA
Chu, S
;
DeRisi, J
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机构:Stanford Univ, Howard Hughes Med Inst, Sch Med, Dept Biochem, Stanford, CA 94305 USA
DeRisi, J
;
Eisen, M
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机构:Stanford Univ, Howard Hughes Med Inst, Sch Med, Dept Biochem, Stanford, CA 94305 USA
Eisen, M
;
Mulholland, J
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机构:Stanford Univ, Howard Hughes Med Inst, Sch Med, Dept Biochem, Stanford, CA 94305 USA
Mulholland, J
;
Botstein, D
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机构:Stanford Univ, Howard Hughes Med Inst, Sch Med, Dept Biochem, Stanford, CA 94305 USA
Botstein, D
;
Brown, PO
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机构:
Stanford Univ, Howard Hughes Med Inst, Sch Med, Dept Biochem, Stanford, CA 94305 USAStanford Univ, Howard Hughes Med Inst, Sch Med, Dept Biochem, Stanford, CA 94305 USA
Brown, PO
;
Herskowitz, I
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机构:Stanford Univ, Howard Hughes Med Inst, Sch Med, Dept Biochem, Stanford, CA 94305 USA