Suppr超能文献

极光 A 耗竭揭示了 中中心体独立的极化机制。

Aurora A depletion reveals centrosome-independent polarization mechanism in .

机构信息

Swiss Institute for Experimental Cancer Research (ISREC), School of Life Sciences, Swiss Federal Institute of Technology Lausanne (EPFL), Lausanne, Switzerland.

Department of Biochemistry, University of Geneva, Geneva, Switzerland.

出版信息

Elife. 2019 Feb 26;8:e44552. doi: 10.7554/eLife.44552.

Abstract

How living systems break symmetry in an organized manner is a fundamental question in biology. In wild-type zygotes, symmetry breaking during anterior-posterior axis specification is guided by centrosomes, resulting in anterior-directed cortical flows and a single posterior PAR-2 domain. We uncover that zygotes depleted of the Aurora A kinase AIR-1 or lacking centrosomes entirely usually establish two posterior PAR-2 domains, one at each pole. We demonstrate that AIR-1 prevents symmetry breaking early in the cell cycle, whereas centrosomal AIR-1 instructs polarity initiation thereafter. Using triangular microfabricated chambers, we establish that bipolarity of () embryos occurs effectively in a cell-shape and curvature-dependent manner. Furthermore, we develop an integrated physical description of symmetry breaking, wherein local PAR-2-dependent weakening of the actin cortex, together with mutual inhibition of anterior and posterior PAR proteins, provides a mechanism for spontaneous symmetry breaking without centrosomes.

摘要

生物体系如何以有序的方式打破对称是生物学的一个基本问题。在野生型合子中,前后轴特化过程中的对称破缺由中心体指导,导致向前的皮质流和单个后部 PAR-2 域。我们发现,缺失 Aurora A 激酶 AIR-1 的合子或完全缺乏中心体的合子通常会在后极各形成一个 PAR-2 域。我们证明 AIR-1 在细胞周期早期阻止对称破缺,而中心体的 AIR-1 随后指导极性起始。利用三角形微加工室,我们确立了()合子的二极性以一种依赖细胞形状和曲率的方式有效地发生。此外,我们提出了一种对称破缺的综合物理描述,其中局部依赖 PAR-2 的肌动蛋白皮层弱化,以及前后 PAR 蛋白的相互抑制,为没有中心体的自发对称破缺提供了一种机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a386/6417861/d6d661635b9c/elife-44552-fig1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验