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驱动蛋白-6 调控细胞大小依赖性纺锤体延伸速度,以保持裂殖酵母有丝分裂时间的恒定。

Kinesin-6 regulates cell-size-dependent spindle elongation velocity to keep mitosis duration constant in fission yeast.

机构信息

Institut Curie, PSL Research University, CNRS, UMR 144, Paris, France.

Department of Cell and Developmental Biology, University of Pennsylvania, Philadelphia, United States.

出版信息

Elife. 2019 Feb 26;8:e42182. doi: 10.7554/eLife.42182.

Abstract

The length of the mitotic spindle scales with cell size in a wide range of organisms during embryonic development. Interestingly, in embryos, this goes along with temporal regulation: larger cells speed up spindle assembly and elongation. We demonstrate that, similarly in fission yeast, spindle length and spindle dynamics adjust to cell size, which allows to keep mitosis duration constant. Since prolongation of mitosis was shown to affect cell viability, this may resemble a mechanism to regulate mitosis duration. We further reveal how the velocity of spindle elongation is regulated: coupled to cell size, the amount of kinesin-6 Klp9 molecules increases, resulting in an acceleration of spindle elongation in anaphase B. In addition, the number of Klp9 binding sites to microtubules increases overproportionally to Klp9 molecules, suggesting that molecular crowding inversely correlates to cell size and might have an impact on spindle elongation velocity control.

摘要

在胚胎发育过程中,有广泛的生物范围中,有丝分裂纺锤体的长度与细胞大小成比例。有趣的是,在 胚胎中,这伴随着时间调节:较大的细胞加速纺锤体组装和伸长。我们证明,类似地在裂殖酵母中,纺锤体长度和纺锤体动力学适应细胞大小,这允许保持有丝分裂持续时间不变。由于有丝分裂的延长被证明会影响细胞活力,这可能类似于调节有丝分裂持续时间的机制。我们进一步揭示了如何调节纺锤体伸长的速度:与细胞大小相结合,增加了驱动蛋白-6 Klp9 分子的数量,导致后期 B 中的纺锤体伸长加速。此外,微管上 Klp9 结合位点的数量与 Klp9 分子不成比例地增加,这表明分子拥挤与细胞大小成反比,可能对纺锤体伸长速度控制有影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08d0/6391065/a571c55f4509/elife-42182-fig1.jpg

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