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斑马鱼原肠胚形成中卵黄合胞体核迁移的货郎模型。

A cargo model of yolk syncytial nuclear migration during zebrafish epiboly.

机构信息

Department of Cell and Systems Biology, University of Toronto, Toronto, ON M5S 3G5, Canada.

Department of Cellular and Physiological Sciences, Life Sciences Institute, Vancouver Campus, 2350 Health Sciences Mall, Vancouver, BC V6T 1Z3, Canada.

出版信息

Development. 2019 Jan 2;146(1):dev169664. doi: 10.1242/dev.169664.

DOI:10.1242/dev.169664
PMID:30509968
Abstract

In teleost fish, the multinucleate yolk syncytial layer functions as an extra-embryonic signaling center to pattern mesendoderm, coordinate morphogenesis and supply nutrients to the embryo. External yolk syncytial nuclei (e-YSN) undergo microtubule-dependent movements that distribute the nuclei over the large yolk mass. How e-YSN migration proceeds, and the role of the yolk microtubules, is not understood, but it is proposed that e-YSN are pulled vegetally as the microtubule network shortens from the vegetal pole. Live imaging revealed that nuclei migrate along microtubules, consistent with a cargo model in which e-YSN are moved down the microtubules by direct association with motor proteins. We found that blocking the plus-end directed microtubule motor kinesin significantly attenuated yolk nuclear movement. Blocking the outer nuclear membrane LINC complex protein Syne2a also slowed e-YSN movement. We propose that e-YSN movement is mediated by the LINC complex, which functions as the adaptor between yolk nuclei and motor proteins. Our work provides new insights into the role of microtubules in morphogenesis of an extra-embryonic tissue and further contributes to the understanding of nuclear migration mechanisms during development.

摘要

在硬骨鱼中,多核卵黄合胞层作为胚胎外信号中心,对中胚层和内胚层进行模式化,协调形态发生,并向胚胎提供营养。外卵黄合胞体细胞核 (e-YSN) 经历微管依赖性运动,将细胞核分布在大的卵黄质上。e-YSN 的迁移过程以及卵黄微管的作用尚不清楚,但据推测,随着微管网络从植物极缩短,e-YSN 会被拉向植物极。实时成像显示,细胞核沿着微管迁移,这与一种货物模型一致,即 e-YSN 通过与马达蛋白的直接结合被沿着微管向下移动。我们发现,阻止正向微管马达驱动蛋白会显著减弱卵黄核的运动。阻止外核膜 LINC 复合物蛋白 Syne2a 也会减缓 e-YSN 的运动。我们提出,e-YSN 的运动是由 LINC 复合物介导的,它作为卵黄核和马达蛋白之间的衔接物发挥作用。我们的工作为微管在胚胎外组织形态发生中的作用提供了新的见解,并进一步促进了对发育过程中核迁移机制的理解。

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