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{"project":"2_test","denotations":[{"id":"17696610-11029058-85497953","span":{"begin":239,"end":241},"obj":"11029058"},{"id":"17696610-17122775-85497954","span":{"begin":739,"end":741},"obj":"17122775"},{"id":"17696610-8893012-85497955","span":{"begin":991,"end":992},"obj":"8893012"},{"id":"17696610-15297881-85497956","span":{"begin":1036,"end":1038},"obj":"15297881"},{"id":"T54062","span":{"begin":239,"end":241},"obj":"11029058"},{"id":"T11603","span":{"begin":739,"end":741},"obj":"17122775"},{"id":"T92230","span":{"begin":991,"end":992},"obj":"8893012"},{"id":"T50789","span":{"begin":1036,"end":1038},"obj":"15297881"}],"text":"The nature of the synapsis checkpoint in male mice remains unidentified. One possible candidate is Dot1 (PCH1 in yeast), a histone methyltransferase silencing factor that is required for pachytene arrest of zip1 and dmc1 mutants in yeast [58], and for preventing RAD54-mediated recombinational DSB repair between sister chromatids. However, DOT1 acts upstream of PCH2. Given that TRIP13 doesn't have checkpoint function in mice, a potential role for mammalian DOT1 in the pachytene checkpoint is dubious but awaits investigation. Recently, it was shown that the TRP53 homolog TRP63 is required for DNA damage–induced death of dictyate-stage primordial oocytes, leading to the suggestion that it is involved in monitoring genome integrity [59]. However, this activity occurs subsequent to a pachytene checkpoint. As alluded to earlier, a complicating problem for studying potential meiotic checkpoint genes in mice is that as in yeast, such genes often have mitotic functions (such as RAD24 [7]), and their ablation can cause lethality [42]. Unless mammalian pachytene checkpoint components have orthologs with similar functions in organisms such as yeast, their identities are likely to remain elusive."}

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