Winey Mark, O'Toole Eileen
Molecular, Cellular and Developmental Biology, University of Colorado at Boulder, Boulder, CO 80309, USA
Molecular, Cellular and Developmental Biology, University of Colorado at Boulder, Boulder, CO 80309, USA The Boulder Laboratory for the 3D EM of Cells, Molecular, Cellular and Developmental Biology, University of Colorado at Boulder, Boulder, CO 80309, USA.
Philos Trans R Soc Lond B Biol Sci. 2014 Sep 5;369(1650). doi: 10.1098/rstb.2013.0457.
Centrioles are among the largest protein-based structures found in most cell types, measuring approximately 250 nm in diameter and approximately 500 nm long in vertebrate cells. Here, we briefly review ultrastructural observations about centrioles and associated structures. At the core of most centrioles is a microtubule scaffold formed from a radial array of nine triplet microtubules. Beyond the microtubule triplets of the centriole, we discuss the critically important cartwheel structure and the more enigmatic luminal density, both found on the inside of the centriole. Finally, we discuss the connectors between centrioles, and the distal and subdistal appendages outside of the microtubule scaffold that reflect centriole age and impart special functions to the centriole. Most of the work we review has been done with electron microscopy or electron tomography of resin-embedded samples, but we also highlight recent work performed with cryoelectron microscopy, cryotomography and subvolume averaging. Significant opportunities remain in the description of centriolar structure, both in mapping of component proteins within the structure and in determining the effect of mutations on components that contribute to the structure and function of the centriole.
中心粒是大多数细胞类型中发现的最大的基于蛋白质的结构之一,在脊椎动物细胞中,其直径约为250纳米,长度约为500纳米。在此,我们简要回顾关于中心粒及相关结构的超微结构观察。大多数中心粒的核心是由九个三联体微管的径向阵列形成的微管支架。除了中心粒的微管三联体,我们还讨论了位于中心粒内部的至关重要的轮辐结构和更神秘的管腔密度。最后,我们讨论中心粒之间的连接物,以及微管支架外部的远端和亚远端附属物,它们反映了中心粒的年龄并赋予中心粒特殊功能。我们回顾的大部分工作是通过对树脂包埋样品进行电子显微镜或电子断层扫描完成的,但我们也强调了最近使用冷冻电子显微镜、冷冻断层扫描和子体积平均法进行的工作。在描述中心粒结构方面仍有重大机遇,这既包括在结构内绘制组成蛋白图谱,也包括确定突变对构成中心粒结构和功能的成分的影响。