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光感受器纤毛及其疾病。

The photoreceptor cilium and its diseases.

机构信息

Institute of Medical Genetics, University of Zurich, Wagistrasse 12, 8952 Schlieren, Zurich, Switzerland; Institute of Molecular Life Sciences, University of Zurich, Winterthurerstrassse 190, 8057 Zurich, Switzerland.

Institute of Molecular Life Sciences, University of Zurich, Winterthurerstrassse 190, 8057 Zurich, Switzerland.

出版信息

Curr Opin Genet Dev. 2019 Jun;56:22-33. doi: 10.1016/j.gde.2019.05.004. Epub 2019 Jun 28.

Abstract

Light sensation occurs in photoreceptor outer segments (OS), which derive from highly specialized primary cilia, based on structural and molecular similarities. Ciliary dysfunction causes ciliopathies, in which retinal degeneration is common. The connecting cilium (CC) is the obligate passage for proteins moving between ciliary and cellular compartment, controlling the correct distribution of proteins on either side of its barrier. While new mechanisms for selective entry of ciliary proteins are being elucidated, active transport out of the OS is increasingly studied. We further discuss other recent advances in the field, such as a role for the CC in docking and fusion of incoming transport vesicles, a newly proposed subcompartmentalization into proximal and distal CC, and mechanisms of OS membrane dynamics paralleling ectosome formation in other cilia.

摘要

光感觉发生在光感受器外段(OS),其来源于高度特化的初级纤毛,基于结构和分子的相似性。纤毛功能障碍导致纤毛病,其中视网膜变性很常见。连接纤毛(CC)是蛋白质在纤毛和细胞区室之间移动的必经之路,控制着其屏障两侧蛋白质的正确分布。虽然新的选择性进入纤毛蛋白的机制正在阐明,但 OS 内的主动运输越来越受到研究。我们还进一步讨论了该领域的其他最新进展,例如 CC 在传入运输小泡的对接和融合中的作用、新提出的近端和远端 CC 亚区室化以及 OS 膜动力学的机制与其他纤毛中的外小体形成平行。

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