Department of Biology, University of Pennsylvania, Philadelphia, PA 19104-6018, USA.
Dev Biol. 2010 May 1;341(1):205-12. doi: 10.1016/j.ydbio.2010.02.027. Epub 2010 Feb 26.
Mouse oocytes acquire the ability to replicate DNA during meiotic maturation, presumably to ensure that DNA replication does not occur precociously between MI and MII and only after fertilization. Acquisition of DNA replication competence requires protein synthesis, but the identity of the proteins required for DNA replication is poorly described. In Xenopus, the only component missing for DNA replication competence is CDC6, which is synthesized from a dormant maternal mRNA recruited during oocyte maturation, and a similar situation also occurs during mouse oocyte maturation. We report that ORC6L is another component required for acquisition of DNA replication competence that is absent in mouse oocytes. The dormant maternal Orc6l mRNA is recruited during maturation via a CPE present in its 3' UTR. RNAi-mediated ablation of maternal Orc6l mRNA prevents the maturation-associated increase in ORC6L protein and inhibits DNA replication in 1-cell embryos. These results suggest that mammalian oocytes have more complex mechanisms to establish DNA replication competence when compared to their Xenopus counterparts.
小鼠卵母细胞在减数分裂成熟过程中获得复制 DNA 的能力,大概是为了确保 DNA 复制不会在 MI 和 MII 之间过早发生,而只在受精后发生。获得 DNA 复制能力需要蛋白质合成,但对于复制 DNA 所需的蛋白质的身份描述得很差。在非洲爪蟾中,唯一缺少的 DNA 复制能力的成分是 CDC6,它是从卵母细胞成熟过程中招募的休眠母体 mRNA 合成的,而在小鼠卵母细胞成熟过程中也存在类似的情况。我们报告说,ORC6L 是另一个获得 DNA 复制能力所必需的成分,而在小鼠卵母细胞中缺失。休眠的母体 Orc6l mRNA 通过其 3'UTR 中的 CPE 在成熟过程中被招募。RNAi 介导的母体 Orc6l mRNA 消融可防止与成熟相关的 ORC6L 蛋白增加,并抑制 1 细胞胚胎中的 DNA 复制。这些结果表明,与非洲爪蟾相比,哺乳动物卵母细胞在建立 DNA 复制能力方面具有更复杂的机制。