兔早期胚胎发育过程中核膜和核膜的阶段依赖性重构

Jens Popken, Volker J Schmid, A. Strauss, T. Guengoer, E. Wolf, V. Zakhartchenko
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引用次数: 5

摘要

利用三维结构照明显微镜,研究了兔早期胚胎发育过程中核内陷的质量和数量以及核孔的分布,并确定了核孔蛋白153 (NUP153)在有丝分裂过程中与染色质相关的确切时间点。与牛早期胚胎细胞核几乎完全内陷含有少量细胞质相反,兔早期胚胎细胞核还显示大量含有大量细胞质的内陷。小体积内陷往往起源于大体积核内陷,而不是相反,表明不同的潜在机制。大体积和小体积核膜内陷需要染色质的存在,因为它们仅限于染色质阳性区域。核仁前体(NPBs)和大体积内陷之间的无染色质接触区没有核孔。小体积内陷未与NPBs接触。每个细胞核内陷和核内囊泡的数量在4细胞期达到高峰。在这一阶段,核表面呈现出高度集中的核孔簇,周围没有核孔的区域。离体核内膜囊泡通常为NUP153阴性。细胞质中随机分布的nup153阳性簇在受精卵时期数量非常丰富,在8细胞期及以后数量逐渐减少,几乎不存在。这些大的NUP153团簇可能代表母系提供的NUP153沉积物,但在有丝分裂期间不可见。在8到16个细胞阶段的主要基因组激活可能标志着从必需的沉积到按需生产的转变。NUP153与染色质的关联是在中期开始的,在膜的再生开始之前。据我们所知,本研究首次证明了兔着床前发育过程中核膜及其下层的主要重塑。
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Stage-dependent remodeling of the nuclear envelope and lamina during rabbit early embryonic development
Utilizing 3D structured illumination microscopy, we investigated the quality and quantity of nuclear invaginations and the distribution of nuclear pores during rabbit early embryonic development and identified the exact time point of nucleoporin 153 (NUP153) association with chromatin during mitosis. Contrary to bovine early embryonic nuclei, featuring almost exclusively nuclear invaginations containing a small volume of cytoplasm, nuclei in rabbit early embryonic stages show additionally numerous invaginations containing a large volume of cytoplasm. Small-volume invaginations frequently emanated from large-volume nuclear invaginations but not vice versa, indicating a different underlying mechanism. Large- and small-volume nuclear envelope invaginations required the presence of chromatin, as they were restricted to chromatin-positive areas. The chromatin-free contact areas between nucleolar precursor bodies (NPBs) and large-volume invaginations were free of nuclear pores. Small-volume invaginations were not in contact with NPBs. The number of invaginations and isolated intranuclear vesicles per nucleus peaked at the 4-cell stage. At this stage, the nuclear surface showed highly concentrated clusters of nuclear pores surrounded by areas free of nuclear pores. Isolated intranuclear lamina vesicles were usually NUP153 negative. Cytoplasmic, randomly distributed NUP153-positive clusters were highly abundant at the zygote stage and decreased in number until they were almost absent at the 8-cell stage and later. These large NUP153 clusters may represent a maternally provided NUP153 deposit, but they were not visible as clusters during mitosis. Major genome activation at the 8- to 16-cell stage may mark the switch from a necessity for a deposit to on-demand production. NUP153 association with chromatin is initiated during metaphase before the initiation of the regeneration of the lamina. To our knowledge, the present study demonstrates for the first time major remodeling of the nuclear envelope and its underlying lamina during rabbit preimplantation development.
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