Hiroshima Research Center for Healthy Aging, Department of Molecular Biotechnology, Graduate School of Advanced Sciences of Matter, Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima, 739-8530, Japan.
Hiroshima Research Center for Healthy Aging, Department of Molecular Biotechnology, Graduate School of Advanced Sciences of Matter, Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima, 739-8530, Japan.
Biochem Biophys Res Commun. 2018 Sep 5;503(2):1160-1167. doi: 10.1016/j.bbrc.2018.06.135. Epub 2018 Jul 2.
The proper organization of microtubules is essential for many cellular functions. Microtubule organization and reorganization are highly regulated during the cell cycle, but the underlying mechanisms remain elusive. Here we characterized unusual interphase microtubule organization in fission yeast nuclear export mutant crm1-124. The mutant cells have an intranuclear microtubule bundle during interphase that pushes the nuclear envelope to assume a protruding morphology. We showed that the formation of this protruding microtubule bundle requires the nuclear accumulation of two microtubule-associated proteins (MAPs), Alp14/TOG and Mal3/EB1. Interestingly, the forced accumulation of Alp14 in the nucleus of wild type cells is sufficient to form the intranuclear microtubule bundle. Furthermore, the frequency of the intranuclear microtubule formation by Alp14 accumulated in the nucleus is prominently increased by a reduction in the nucleation activity of interphase cytoplasmic microtubules. We propose that properly regulated nucleocytoplasmic transport and maintained activity of cytoplasmic microtubule nucleation during interphase are important for the proper organization of interphase cytoplasmic microtubules.
微管的正确组织对于许多细胞功能至关重要。微管组织和重组在细胞周期中受到高度调节,但潜在的机制仍难以捉摸。在这里,我们描述了裂殖酵母核输出突变体 crm1-124 中异常的间期微管组织。突变细胞在间期具有核内微管束,将核膜推至突出形态。我们表明,这种突起微管束的形成需要两种微管相关蛋白(MAPs)Alp14/TOG 和 Mal3/EB1 的核积累。有趣的是,野生型细胞中 Alp14 的强制核积累足以形成核内微管束。此外,通过降低间期细胞质微管成核活性,Alp14 在核内积累形成核内微管的频率显著增加。我们提出,适当调节核质运输和维持间期细胞质微管成核活性对于间期细胞质微管的正确组织是重要的。