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仓鼠早期胚胎中的核形态发生与转录活性的起始

Nuclear morphogenesis and the onset of transcriptional activity in early hamster embryos.

作者信息

Ferreira J, Carmo-Fonseca M

机构信息

Institute of Histology and Embryology, Faculty of Medicine, University of Lisbon, 1699 Lisboa codex, Portugal.

出版信息

Chromosoma. 1996 Jul;105(1):1-11. doi: 10.1007/BF02510033.

DOI:10.1007/BF02510033
PMID:8662253
Abstract

Coiled bodies and interchromatin granules are distinct subnuclear domains that contain splicing small nuclear ribonucleoproteins (snRNPs) and protein-splicing factors. Here we have studied the morphogenesis of coiled bodies and clusters of interchromatin granules in relation to the onset of transcriptional activity in early hamster embryos. The results indicate that major embryonic transcription by RNA polymerase II is first detected during the early two-cell stage (15-20 h post-fertilization), whereas RNA polymerase I activity and nucleologenesis are only observed in late two-cell embryos (30-40 h postfertilization). Splicing snRNPs and heterogeneous nuclear RNP (hnRNP) proteins are shown to be imported into the pronuclei following fertilization, and prominent clusters of interchromatin granules containing the splicing factor SC-35 are already observed in both maternal and paternal pronuclei of one-cell embryos. Interestingly, these large clusters of interchromatin granules do not appear to concentrate splicing snRNPs. In contrast, coiled bodies are first detected during the two-cell stage after the onset of transcription, and they are clearly enriched in snRNPs. Taken together with results previously obtained in mouse embryos, these data suggest that the assembly of coiled bodies and clusters of interchromatin granules is independent from the onset of embryonic transcriptional activity, and that coiled bodies represent the major snRNP-enriched subnuclear domain in the early mammalian embryo.

摘要

卷曲小体和染色质间颗粒是不同的亚核结构域,它们包含剪接小核核糖核蛋白(snRNP)和蛋白质剪接因子。在此,我们研究了卷曲小体和染色质间颗粒簇的形态发生与早期仓鼠胚胎转录活性起始之间的关系。结果表明,RNA聚合酶II介导的主要胚胎转录最早在二细胞早期(受精后15 - 20小时)被检测到,而RNA聚合酶I活性和核仁发生仅在二细胞晚期胚胎(受精后30 - 40小时)中观察到。剪接snRNP和不均一核核糖核蛋白(hnRNP)在受精后被导入原核,并且在单细胞胚胎的雌原核和雄原核中均已观察到含有剪接因子SC - 35的明显的染色质间颗粒簇。有趣的是,这些大的染色质间颗粒簇似乎并不富集剪接snRNP。相比之下,卷曲小体在转录起始后的二细胞阶段首次被检测到,并且它们明显富含snRNP。结合先前在小鼠胚胎中获得的结果,这些数据表明卷曲小体和染色质间颗粒簇的组装独立于胚胎转录活性的起始,并且卷曲小体代表早期哺乳动物胚胎中主要富含snRNP的亚核结构域。

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Nuclear distribution of RNA polymerase II and mRNA processing machinery in early mammalian embryos.RNA聚合酶II和mRNA加工机制在早期哺乳动物胚胎中的核分布。
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An immunocytochemical study of interchromatin granule clusters in early mouse embryos.早鼠胚胎中染色质间颗粒簇的免疫细胞化学研究。

本文引用的文献

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Perichromatin fibrils are in situ forms of nascent transcripts.染色质周边纤维是新生转录本的原位形式。
Trends Cell Biol. 1994 Mar;4(3):86-90. doi: 10.1016/0962-8924(94)90180-5.
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The coiled body.卷曲小体
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Fluorescent labeling of nascent RNA reveals transcription by RNA polymerase II in domains scattered throughout the nucleus.新生RNA的荧光标记显示RNA聚合酶II在分散于整个细胞核的区域中进行转录。
J Cell Biol. 1993 Jul;122(2):283-93. doi: 10.1083/jcb.122.2.283.
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Non-snRNP protein splicing factors.非snRNP蛋白剪接因子
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Macromolecular domains within the cell nucleus.细胞核内的大分子结构域
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Localisation of splicing snRNPs in mammalian cells.剪接小核核糖核蛋白在哺乳动物细胞中的定位
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Differential interaction of splicing snRNPs with coiled bodies and interchromatin granules during mitosis and assembly of daughter cell nuclei.有丝分裂过程中剪接小核核糖核蛋白与卷曲小体和染色质间颗粒的差异相互作用以及子细胞核的组装
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