Laurincik J, Thomsen P D, Hay-Schmidt A, Avery B, Greve T, Ochs R L, Hyttel P
Research Institute of Animal Production, SK-949 92 Nitra, Slovak Republic.
Biol Reprod. 2000 Apr;62(4):1024-32. doi: 10.1095/biolreprod62.4.1024.
The aim of the present investigation was to describe the basic cell biology of the postfertilization activation of rRNA genes using in vitro-produced bovine embryos as a model. We used immunofluorescence confocal laser scanning microscopy and transmission electron microscopy to study nucleolar development in the nuclei of embryos up to the fifth postfertilization cell cycle. During the first cell cycle (1-cell stage), fibrillarin, upstream binding factor (UBF), nucleolin (C23), and RNA polymerase I were localized to distinct foci in the pronuclei, and, ultrastructurally, compact spherical fibrillar masses were the most prominent pronuclear finding. During the second cell cycle (2-cell stage), the findings were similar except for a lack of nucleolin and RNA polymerase I labeling. During the third cell cycle (4-cell stage), fibrillarin, UBF, nucleophosmin, and nucleolin were localized to distinct foci. Ultrastructurally, spherical fibrillar masses that developed a central vacuole over the course of the cell cycle were observed. Early in the fourth cell cycle (8-cell stage), fibrillarin, nucleophosmin, and nucleolin were localized to small bodies that with time developed a central vacuole. UBF and topoisomerase I were localized to clusters of small foci. Ultrastructurally, spherical fibrillar masses with a large eccentric vacuole and later small peripheral vacuoles were seen. Late in the fourth cell cycle, nucleophosmin and nucleolin were localized to large shell-like bodies; and fibrillarin, UBF, topoisomerase I, and RNA polymerase I were localized to clusters of small foci. Ultrastructurally, a presumptive dense fibrillar component (DFC) and fibrillar centers (FCs) were observed peripherally in the vacuolated spherical fibrillar masses. Subsequently, the presumptive granular component (GC) gradually became embedded in the substance of this entity, resulting in the formation of a fibrillo-granular nucleolus. During the fifth cell cycle (16-cell stage), a spherical fibrillo-granular nucleolus developed from the start of the cell cycle. In conclusion, the nucleolar protein compartment in in vitro-produced preimplantation bovine embryos is assembled over several cell cycles. In particular, RNA polymerase I and topoisomerase I are detected for the first time late during the fourth embryonic cell cycle, which coincides with the first recognition of the DFC, FCs, and GC at the ultrastructural level.
本研究的目的是以体外生产的牛胚胎为模型,描述受精后核糖体RNA(rRNA)基因激活的基本细胞生物学过程。我们使用免疫荧光共聚焦激光扫描显微镜和透射电子显微镜,研究了受精后直至第五个细胞周期的胚胎细胞核中的核仁发育情况。在第一个细胞周期(1细胞期),纤维蛋白、上游结合因子(UBF)、核仁素(C23)和RNA聚合酶I定位于原核中的不同位点,并且在超微结构上,紧密的球形纤维状团块是原核中最显著的发现。在第二个细胞周期(2细胞期),除了缺乏核仁素和RNA聚合酶I标记外,其他发现相似。在第三个细胞周期(4细胞期),纤维蛋白、UBF、核磷蛋白和核仁素定位于不同位点。在超微结构上,观察到在细胞周期过程中形成中央液泡的球形纤维状团块。在第四个细胞周期早期(8细胞期),纤维蛋白、核磷蛋白和核仁素定位于随时间推移形成中央液泡的小体。UBF和拓扑异构酶I定位于小位点簇。在超微结构上,可见具有大的偏心液泡和随后的小周边液泡的球形纤维状团块。在第四个细胞周期后期,核磷蛋白和核仁素定位于大的壳状小体;纤维蛋白、UBF、拓扑异构酶I和RNA聚合酶I定位于小位点簇。在超微结构上,在空泡化的球形纤维状团块的周边观察到推测的致密纤维成分(DFC)和纤维中心(FC)。随后,推测的颗粒成分(GC)逐渐嵌入该实体的物质中,导致形成纤维颗粒状核仁。在第五个细胞周期(16细胞期),从细胞周期开始就形成了球形纤维颗粒状核仁。总之,体外生产的植入前牛胚胎中的核仁蛋白区室是在几个细胞周期中组装而成的。特别是,在第四个胚胎细胞周期后期首次检测到RNA聚合酶I和拓扑异构酶I,这与在超微结构水平上首次识别DFC、FC和GC相吻合。