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ARL13B 从初级纤毛外调节 Sonic hedgehog 信号通路。

ARL13B regulates Sonic hedgehog signaling from outside primary cilia.

机构信息

Neuroscience Graduate Program, Emory University School of Medicine, Atlanta, United States.

Department of Human Genetics, Emory University School of Medicine, Atlanta, United States.

出版信息

Elife. 2020 Mar 4;9:e50434. doi: 10.7554/eLife.50434.

Abstract

ARL13B is a regulatory GTPase highly enriched in cilia. Complete loss of disrupts cilia architecture, protein trafficking and Sonic hedgehog signaling. To determine whether ARL13B is required within cilia, we knocked in a cilia-excluded variant of ARL13B (V358A) and showed it retains all known biochemical function. We found that ARL13B protein was expressed but could not be detected in cilia, even when retrograde ciliary transport was blocked. We showed mice are viable and fertile with normal Shh signal transduction. However, in contrast to wild type cilia, cells displayed short cilia and lacked ciliary ARL3 and INPP5E. These data indicate that ARL13B's role within cilia can be uncoupled from its function outside of cilia. Furthermore, these data imply that the cilia defects upon complete absence of ARL13B do not underlie the alterations in Shh transduction, which is unexpected given the requirement of cilia for Shh transduction.

摘要

ARL13B 是一种在纤毛中高度富集的调节 GTPase。完全缺失 会破坏纤毛结构、蛋白质运输和 Sonic hedgehog 信号转导。为了确定 ARL13B 是否在纤毛内需要,我们敲入了一种纤毛排除的 ARL13B 变体(V358A),并表明它保留了所有已知的生化功能。我们发现 ARL13B 蛋白表达,但在纤毛中无法检测到,即使逆行纤毛运输被阻断。我们表明 小鼠具有活力和生育能力,Shh 信号转导正常。然而,与野生型纤毛相比, 细胞显示短纤毛,并且缺乏纤毛 ARL3 和 INPP5E。这些数据表明,ARL13B 在纤毛内的作用与其在纤毛外的功能可以分离。此外,这些数据表明,完全缺失 ARL13B 时纤毛缺陷不会导致 Shh 转导的改变,这与 Shh 转导需要纤毛的要求不一致,令人意外。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/200a/7075693/207261d2872a/elife-50434-fig1.jpg

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