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进化比较揭示了线虫胚胎纺锤体极摆动的位置转换。

Evolutionary comparisons reveal a positional switch for spindle pole oscillations in Caenorhabditis embryos.

机构信息

Laboratory of Molecular Biology of the Cell, UMR5239, Ecole Normale Supérieure de Lyon, Centre National de la Recherche Scientifique, 69007 Lyon, France.

出版信息

J Cell Biol. 2013 May 27;201(5):653-62. doi: 10.1083/jcb.201210110. Epub 2013 May 20.

DOI:10.1083/jcb.201210110
PMID:23690175
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3664713/
Abstract

During the first embryonic division in Caenorhabditis elegans, the mitotic spindle is pulled toward the posterior pole of the cell and undergoes vigorous transverse oscillations. We identified variations in spindle trajectories by analyzing the outwardly similar one-cell stage embryo of its close relative Caenorhabditis briggsae. Compared with C. elegans, C. briggsae embryos exhibit an anterior shifting of nuclei in prophase and reduced anaphase spindle oscillations. By combining physical perturbations and mutant analysis in both species, we show that differences can be explained by interspecies changes in the regulation of the cortical Gα-GPR-LIN-5 complex. However, we found that in both species (1) a conserved positional switch controls the onset of spindle oscillations, (2) GPR posterior localization may set this positional switch, and (3) the maximum amplitude of spindle oscillations is determined by the time spent in the oscillating phase. By investigating microevolution of a subcellular process, we identify new mechanisms that are instrumental to decipher spindle positioning.

摘要

在秀丽隐杆线虫的第一次胚胎分裂过程中,有丝分裂纺锤体被拉向细胞的后端,并经历剧烈的横向振荡。我们通过分析其近亲秀丽隐杆线虫的向外相似的单细胞胚胎来识别纺锤体轨迹的变化。与秀丽隐杆线虫相比,秀丽隐杆线虫胚胎在前期表现出核的向前移位和后期纺锤体振荡减少。通过在两个物种中结合物理干扰和突变分析,我们表明差异可以通过物种间皮层 Gα-GPR-LIN-5 复合物调节的变化来解释。然而,我们发现,在两个物种中:(1)一个保守的位置开关控制着纺锤体振荡的开始;(2)GPR 后端定位可能设定了这个位置开关;(3)纺锤体振荡的最大幅度取决于振荡阶段所花费的时间。通过研究一个亚细胞过程的微观进化,我们确定了新的机制,这些机制对阐明纺锤体定位至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c43/3664713/548910f4627e/JCB_201210110R_Fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c43/3664713/a81f029dd319/JCB_201210110_Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c43/3664713/96b9554e1398/JCB_201210110_Fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c43/3664713/67c8fa2be767/JCB_201210110_Fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c43/3664713/347bdffc3148/JCB_201210110_Fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c43/3664713/548910f4627e/JCB_201210110R_Fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c43/3664713/a81f029dd319/JCB_201210110_Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c43/3664713/96b9554e1398/JCB_201210110_Fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c43/3664713/67c8fa2be767/JCB_201210110_Fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c43/3664713/347bdffc3148/JCB_201210110_Fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c43/3664713/548910f4627e/JCB_201210110R_Fig5.jpg

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本文引用的文献

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Dynamic localization of C. elegans TPR-GoLoco proteins mediates mitotic spindle orientation by extrinsic signaling.线虫 TPR-GoLoco 蛋白的动态定位通过外在信号来介导有丝分裂纺锤体的定向。
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A novel mechanism of microtubule length-dependent force to pull centrosomes toward the cell center.
微管反馈和 LET-99 依赖性的拉力控制确保纺锤体位置的稳健性。
Biophys J. 2018 Dec 4;115(11):2189-2205. doi: 10.1016/j.bpj.2018.10.010. Epub 2018 Oct 19.
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Workshop report: Caenorhabditis nematodes as model organisms to study trait variation and its evolution.研讨会报告:秀丽隐杆线虫作为研究性状变异及其进化的模式生物
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