...
首页> 外文期刊>Human reproduction update >The molecular foundations of the maternal to zygotic transition in the preimplantation embryo.
【24h】

The molecular foundations of the maternal to zygotic transition in the preimplantation embryo.

机译:植入前胚胎中母体向合子过渡的分子基础。

获取原文
获取原文并翻译 | 示例
           

摘要

The maternal to zygotic transition is the first major transition that occurs following fertilization, and entails a dramatic reprogramming of gene expression that is essential for continued development. Although the major reprogramming of gene expression occurs during the 2-cell stage, transcription is evident in the 1-cell embryo, with the male pronucleus supporting a significantly higher level of transcription than the female pronucleus. This difference is likely due to differences in chromatin structure as a consequence of the protamine-histone exchange. Although the 1-cell embryo is transcriptionally competent, transcription and translation appear uncoupled. This transcription, however, may mark promoters for efficient utilization in the 2-cell embryo. Genome activation in the 2-cell embryo is accompanied by a requirement for an enhancer for efficient transcription and the more efficient utilization of TATA-less promoters. These changes in promoter utilization could contribute substantially to the reprogramming of gene expression. Superimposed on genome activation is the development of a chromatin-mediated transcriptionally repressive state that is relieved by either inducing histone hyperacetylation or inhibiting the second round of DNA replication. Since genome activation appears to be a relatively opportunistic process, the development of the transcriptionally repressive state may be a major determinant in establishing the appropriate gene expression profile that is essential for continued development.
机译:从母体到合子的过渡是受精后发生的第一个主要过渡,需要对基因表达进行戏剧性的重编程,这对于持续发展至关重要。尽管基因表达的主要重编程发生在2细胞阶段,但转录在1细胞胚胎中很明显,雄性原核比雌性原核支持明显更高的转录水平。这种差异可能是由于鱼精蛋白-组蛋白交换导致的染色质结构差异。尽管1细胞胚胎具有转录能力,但转录和翻译似乎是不耦合的。但是,该转录可能标记了在2细胞胚胎中有效利用的启动子。在2-细胞胚胎中的基因组激活伴随着对有效转录的增强子的需求,并且需要更高效地利用无TATA的启动子。启动子利用的这些变化可大大有助于基因表达的重编程。叠加在基因组激活上的是染色质介导的转录抑制状态的发展,该状态可通过诱导组蛋白超乙酰化或抑制第二轮DNA复制来缓解。由于基因组激活似乎是一个相对机会性的过程,转录抑制状态的发展可能是建立适当的基因表达谱的主要决定因素,而这种基因表达谱对于持续发展至关重要。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号