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裂殖酵母细胞如何生长并将生长与有丝分裂周期联系起来?

How do fission yeast cells grow and connect growth to the mitotic cycle?

作者信息

Sveiczer Ákos, Horváth Anna

机构信息

Department of Applied Biotechnology and Food Science, Budapest University of Technology and Economics, Szt. Gellért tér 4, Budapest, 1111, Hungary.

出版信息

Curr Genet. 2017 May;63(2):165-173. doi: 10.1007/s00294-016-0632-0. Epub 2016 Jul 27.

DOI:10.1007/s00294-016-0632-0
PMID:27465359
Abstract

To maintain size homeostasis in a unicellular culture, cells should coordinate growth to the division cycle. This is achieved via size control mechanisms (also known as size checkpoints), i.e. some events during the mitotic cycle supervene only if the cell has reached a critical size. Rod-shaped cells like those of fission yeast are ideal model organisms to study these checkpoints via time-lapse microphotography. By applying this method, once we can analyse the growth process between two consecutive divisions at a single (or even at an 'average') cellular level, moreover, we can also position the size checkpoint(s) at the population level. Finally, any of these controls can be abolished in appropriate cell cycle mutants, either in steady-state or in induction synchronised cultures. In the latter case, we produce abnormally oversized cells, and microscopic experiments with them clearly show the existence of a critical size above which the size checkpoint ceases (becomes cryptic). In this review, we delineate the development of our knowledge both on the growth mode of fission yeast and on the operating size control(s) during its mitotic cycle. We finish these historical stories with our recent findings, arguing that three different size checkpoints exist in the fission yeast cell cycle, namely in late G1, in mid G2 and in late G2, which has been concluded by analysing these controls in several cell cycle mutants.

摘要

为了在单细胞培养中维持大小稳态,细胞应将生长与分裂周期协调起来。这是通过大小控制机制(也称为大小检查点)实现的,即只有当细胞达到临界大小时,有丝分裂周期中的某些事件才会发生。像裂殖酵母那样的杆状细胞是通过延时显微摄影来研究这些检查点的理想模式生物。通过应用这种方法,我们不仅可以在单个(甚至“平均”)细胞水平上分析两个连续分裂之间的生长过程,而且还可以在群体水平上定位大小检查点。最后,在稳态或诱导同步培养的适当细胞周期突变体中,任何这些控制都可以被消除。在后一种情况下,我们会产生异常超大的细胞,对它们进行的显微实验清楚地表明存在一个临界大小,超过这个大小,大小检查点就会停止(变得隐匿)。在这篇综述中,我们阐述了我们对裂殖酵母生长模式及其有丝分裂周期中运行的大小控制的认识发展。我们用我们最近的发现结束这些历史故事,认为在裂殖酵母细胞周期中存在三个不同的大小检查点,即在G1晚期、G2中期和G2晚期,这是通过分析几个细胞周期突变体中的这些控制得出的结论。

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