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首页> 外文期刊>Current Biology: CB >Spindle Pole Body History Intrinsically Links Pole Identity with Asymmetric Fate in Budding Yeast
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Spindle Pole Body History Intrinsically Links Pole Identity with Asymmetric Fate in Budding Yeast

机译:主轴的极体历史内在地将极身份与萌发酵母中的不对称命运联系起来

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摘要

Background: Budding yeast is a unique model for exploring differential fate in a cell dividing asymmetrically. In yeast, spindle orientation begins with the old spindle pole body (SPB) (from the preceding cell cycle) contacting the bud by its existing astral nnicrotubules (aMTs) while the new pole delays astral microtubule organization. This appears to prime the inheritance of the old pole by the bud. The basis for this asymmetry and the discrimination of the poles by virtue of their history remain a mystery. Results: Here, we report that asymmetric aMT organization stems from an outstanding structural asymmetry linked to the SPB cycle. We show that the gamma-tubulin nucleation complex (gamma TC) favors the old spindle pole, an asymmetry inherent to the outer plaque (the cytoplasmic face of the SPB). Indeed, Spc72 (the receptor for the gamma TC) is acquired by the new SPB outer plaque partway through spindle assembly. The significance of this asymmetry was explored in cells expressing an Spc72(1-276)-Cnm67 fusion that forced symmetric nucleation at the SPB outer plaques. This manipulation triggered simultaneous aMT organization by both spindle poles from the outset and led to symmetric contacts between poles and the bud, effectively disrupting the program for spindle polarity. Temporally symmetric aMT organization perturbed Kar9 polarization by randomizing the choice of the pole to be guided toward the bud. Accordingly, the pattern of SPB inheritance was also randomized. Conclusions: Spc72 differential recruitment imparting asymmetric aMT organization represents the most upstream determinant linking SPB historical identity and fate.
机译:背景:芽芽酵母是探索不对称分裂细胞中不同命运的独特模型。在酵母中,纺锤定向始于旧的纺锤极体(SPB)(来自先前的细胞周期)通过其现有的星状微管(aMT)与芽接触,而新的杆延迟了星状微管的组织。这似乎预示着芽对旧杆的继承。这种不对称性的基础以及两极凭借其历史而受到的歧视仍然是一个谜。结果:在这里,我们报告不对称aMT组织源于与SPB周期相关的突出结构不对称。我们显示,γ-微管蛋白成核复合物(γTC)有利于旧的纺锤体极,这是外斑块固有的不对称性(SPB的细胞质面)。确实,Spc72(γTC的受体)是在纺锤体组装的途中被新的SPB外板获得的。这种不对称的重要性已在表达Spc72(1-276)-Cnm67融合体的细胞中进行了探索,该融合体在SPB外部噬菌斑上迫使对称成核。这种操作从一开始就触发了两个主轴同时进行的aMT组织,并导致了杆和芽之间的对称接触,从而有效地破坏了主轴极性的程序。临时对称的aMT组织通过随机选择朝向芽的极点来扰乱Kar9极化。因此,SPB遗传模式也被随机化。结论:赋予不对称aMT组织的Spc72差异募集代表了联系SPB历史身份和命运的最上游决定因素。

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