在小鼠胚胎发育的第一个细胞周期中,小核糖核蛋白颗粒(snRNPs)的重新定位独立于RNA合成、DNA合成和细胞质分裂

Wendy L. Dean, Gilbert A. Schultz
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引用次数: 14

摘要

研究了细胞松弛素D、阿飞霉素和α-amanitin处理小鼠受精卵后,小核核糖核蛋白颗粒(snRNPs)在小鼠胚胎发育第一个细胞周期中的定位过程。通过间接免疫荧光评估,snRNPs在处理过的胚胎细胞核中的积累模式不受抑制剂的影响。结果表明,在第一个细胞周期中snRNPs的定位不需要持续的细胞分裂、DNA复制或RNA聚合酶II基因的转录。这些发现表明,母源snRNPs在受精卵基因组转录重新启动之前定位于受精卵的细胞核,并且在胚胎基因组的遗传活性在早期2细胞阶段被激活时,需要加工信使RNA前体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Relocalization of small ribonucleoprotein particles (snRNPs) during the first cell cycle of mouse embryo development is independent of RNA synthesis, DNA synthesis and cytokinesis

The process of localization of small nuclear ribonucleoprotein particles (snRNPs) during the first cell cycle of mouse embryo development was investigated following treatment of fertilized eggs with cytochalasin D, aphidicolin and α-amanitin. The pattern of accumulation of snRNPs in nuclei of treated embryos as assessed by indirect immunofluorescence was unaffected by the inhibitors. The results demonstrate that the localization of snRNPs during the first cell cyle does not require ongoing cytokinesis, DNA replication or transcription of RNA polymerase II genes. These findings suggest that maternally derived snRNPs become localized to the nucleus of the fertilized ovum prior to the reinitiation of transcription from the zygote genome and are required for processing of messenger RNA precursors when genetic activity of the embryonic genome is activated at the early 2-cell stage.

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