Institute of Biochemistry, ETH Zurich, Otto-Stern-Weg 3, 8093, Zurich, Switzerland.
David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
Bioessays. 2018 Aug;40(8):e1800038. doi: 10.1002/bies.201800038. Epub 2018 Jul 5.
Asymmetric cell division generates cell diversity and contributes to cellular aging and rejuvenation. Here, we review the molecular mechanisms enabling budding yeast to recognize spindle pole bodies (SPB, centrosome equivalent) based on their age, and guide their non-random mitotic segregation: SPB inheritance requires the distinction of old from new SPBs and is regulated by the SPB-inheritance network (SPIN) and the mitotic exit network (MEN). The SPIN marks the pre-existing SPB as old and the MEN recognizes these marks translating them into spindle orientation. We next revisit other molecules and structures that partition depending on their age rather than their abundance at mitosis as, for example, DNA, centrosomes, mitochondria, and histones in yeast and other systems. The recurrence of this differential behavior suggests a functional significance for numerous cell types, which we then discuss. We conclude that non-random segregation may facilitate asymmetric cell fate determination and thereby indirectly aging and rejuvenation. Also see the video abstract here: https://youtu.be/1sQ4rAomnWY.
不对称细胞分裂产生细胞多样性,并有助于细胞衰老和恢复活力。在这里,我们回顾了使芽殖酵母能够根据其年龄识别出纺锤体极体(SPB,中心体等价物)并指导其非随机有丝分裂分离的分子机制:SPB 遗传需要区分新旧 SPB,并受 SPB 遗传网络 (SPIN) 和有丝分裂退出网络 (MEN) 的调节。SPIN 将预先存在的 SPB 标记为旧的,MEN 识别这些标记并将其转化为纺锤体定向。接下来,我们重新审视了其他根据年龄而不是在有丝分裂时的丰度进行分配的分子和结构,例如酵母和其他系统中的 DNA、中心体、线粒体和组蛋白。这种差异行为的反复出现表明它对许多细胞类型具有功能意义,我们将在下文讨论。我们得出的结论是,非随机分离可能有助于不对称细胞命运的决定,从而间接地影响衰老和恢复活力。也可在此处观看视频摘要:https://youtu.be/1sQ4rAomnWY。