Suppr超能文献

中心粒SAS-7在SPD-2上游发挥作用,以调控中心粒组装和中心粒周围物质形成。

Centriolar SAS-7 acts upstream of SPD-2 to regulate centriole assembly and pericentriolar material formation.

作者信息

Sugioka Kenji, Hamill Danielle R, Lowry Joshua B, McNeely Marie E, Enrick Molly, Richter Alyssa C, Kiebler Lauren E, Priess James R, Bowerman Bruce

机构信息

Institute of Molecular Biology, University of Oregon, Eugene, United States.

Department of Zoology, Ohio Wesleyan University, Delaware, United States.

出版信息

Elife. 2017 Jan 16;6:e20353. doi: 10.7554/eLife.20353.

Abstract

The centriole/basal body is a eukaryotic organelle that plays essential roles in cell division and signaling. Among five known core centriole proteins, SPD-2/Cep192 is the first recruited to the site of daughter centriole formation and regulates the centriolar localization of the other components in and in humans. However, the molecular basis for SPD-2 centriolar localization remains unknown. Here, we describe a new centriole component, the coiled-coil protein SAS-7, as a regulator of centriole duplication, assembly and elongation. Intriguingly, our genetic data suggest that SAS-7 is required for daughter centrioles to become competent for duplication, and for mother centrioles to maintain this competence. We also show that SAS-7 binds SPD-2 and regulates SPD-2 centriolar recruitment, while SAS-7 centriolar localization is SPD-2-independent. Furthermore, pericentriolar material (PCM) formation is abnormal in mutants, and the PCM-dependent induction of cell polarity that defines the anterior-posterior body axis frequently fails. We conclude that SAS-7 functions at the earliest step in centriole duplication yet identified and plays important roles in the orchestration of centriole and PCM assembly.

摘要

中心粒/基体是一种真核细胞器,在细胞分裂和信号传导中发挥着重要作用。在已知的五种核心中心粒蛋白中,SPD-2/Cep192是第一个被招募到子中心粒形成位点的蛋白,并在秀丽隐杆线虫和人类中调节其他组分在中心粒上的定位。然而,SPD-2在中心粒上定位的分子基础仍然未知。在此,我们描述了一种新的中心粒组分,即卷曲螺旋蛋白SAS-7,它是中心粒复制、组装和延长的调节因子。有趣的是,我们的遗传学数据表明,SAS-7是子中心粒具备复制能力所必需的,也是母中心粒维持这种能力所必需的。我们还表明,SAS-7与SPD-2结合并调节SPD-2在中心粒上的招募,而SAS-7在中心粒上的定位不依赖于SPD-2。此外,在SAS-7突变体中,中心粒外周物质(PCM)的形成是异常的,并且定义前后体轴的PCM依赖性细胞极性诱导经常失败。我们得出结论,SAS-7在已确定的中心粒复制的最早步骤中发挥作用,并在中心粒和PCM组装的协调过程中发挥重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51e2/5342823/6c3e0e34dcc9/elife-20353-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