Kopecný V, Fakan S, Pavlok A, Pivko J, Grafenau P, Biggiogera M, Leser G, Martin T E
Centre of Electron Microscopy, University of Lausanne, Switzerland.
Mol Reprod Dev. 1991 Jul;29(3):209-19. doi: 10.1002/mrd.1080290302.
Small nuclear ribonucleoproteins (snRNPs) were localized using human autoimmune or monoclonal anti-snRNP antibodies and ultrastructural immunocytochemistry in early preimplantation bovine embryos before and at transcription onset. Bovine cleavage stages up to 16-cell embryos were obtained either by culture of in vitro-fertilized ovarian oocytes or by isolation at slaughter of embryos fertilized and developed in vivo. Before transcription onset, up to the four-cell stage, diffuse labeling of nucleoplasm was detected, whereas cytoplasm labeling remained low. At the transcription onset, labeling of all eight-cell embryo nuclei was markedly concentrated at the borderline of already formed, condensed chromatin aggregates, where it was associated mainly with perichromatin fibrils. The condensed chromatin blocks revealed by several different staining methods were more prominent than is the case in most somatic cells. The degree of chromatin condensation and the pattern of its distribution differed between in vivo- and in vitro-produced eight-cell embryos: the in vitro embryos showed a higher degree of chromatin condensation and a peripheral distribution of chromatin blocks. A relation of this observation to the developmental potential of cow embryos is suggested. In two- and four-cell embryos, intensive labeling was seen in interchromatin granules, which, in their turn, were often seen in close proximity to the nucleolus precursor bodies, or in the four-cell stage were interconnected to them. No labeling was ever seen, using antibodies specific for the snRNP Sm antigen, in nucleolar precursor bodies during embryonic nucleologenesis nor in the resulting nucleoli. There was some incidental labeling of the large central vacuole appearing at the beginning of the nucleolus precursor body transformation, testifying the nucleoplasmic origin of this entity.
利用人类自身免疫或单克隆抗snRNP抗体以及超微结构免疫细胞化学方法,对植入前早期牛胚胎在转录开始前和转录开始时的小核核糖核蛋白(snRNPs)进行定位。通过体外受精的卵巢卵母细胞培养或在屠宰时分离体内受精并发育的胚胎,获得直至16细胞胚胎的牛卵裂阶段。在转录开始前,直至四细胞阶段,检测到核质的弥漫性标记,而细胞质标记仍然很低。在转录开始时,所有八细胞胚胎细胞核的标记明显集中在已形成的浓缩染色质聚集体的边界处,主要与染色质周围纤维相关。通过几种不同染色方法揭示的浓缩染色质块比大多数体细胞中的情况更明显。体内和体外产生的八细胞胚胎之间,染色质浓缩程度及其分布模式有所不同:体外胚胎显示出更高程度的染色质浓缩和染色质块的周边分布。提示了这一观察结果与牛胚胎发育潜能的关系。在二细胞和四细胞胚胎中,在染色质间颗粒中可见强烈标记,而这些颗粒又常常靠近核仁前体,或在四细胞阶段与核仁前体相互连接。在胚胎核仁形成过程中,使用针对snRNP Sm抗原的特异性抗体,在核仁前体或由此产生的核仁中从未观察到标记。在核仁前体转化开始时出现的大中央液泡有一些偶然标记,证明了该实体的核质起源。