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GPSM2-GNAI 特异指定最长的静纤毛并定义毛细胞束列的身份。

GPSM2-GNAI Specifies the Tallest Stereocilia and Defines Hair Bundle Row Identity.

机构信息

The Jackson Laboratory, Bar Harbor, ME 04609, USA.

Department of Ophthalmology and Visual Sciences, Moran Eye Center, University of Utah, Salt Lake City, UT 84132, USA.

出版信息

Curr Biol. 2019 Mar 18;29(6):921-934.e4. doi: 10.1016/j.cub.2019.01.051. Epub 2019 Feb 28.

Abstract

The transduction compartment of inner ear hair cells, the hair bundle, is composed of stereocilia rows of graded height, a property essential for sensory function that remains poorly understood at the molecular level. We previously showed that GPSM2-GNAI is enriched at stereocilia distal tips and required for their postnatal elongation and bundle morphogenesis-two characteristics shared with MYO15A (short isoform), WHRN, and EPS8 proteins. Here we first performed a comprehensive genetic analysis of the mouse auditory epithelium to show that GPSM2, GNAI, MYO15A, and WHRN operate in series within the same pathway. To understand how these functionally disparate proteins act as an obligate complex, we then systematically analyzed their distribution in normal and mutant bundles over time. We discovered that WHRN-GPSM2-GNAI is an extra module recruited by and added to a pre-existing MYO15A-EPS8 stereocilia tip complex. This extended complex is only present in the first, tallest row, and is required to stabilize larger amounts of MYO15A-EPS8 than in shorter rows, which at tips harbor only MYO15A-EPS8. In the absence of GPSM2 or GNAI function, including in the epistatic Myo15a and Whrn mutants, bundles retain an embryonic-like organization that coincides with generic stereocilia at the molecular level. We propose that GPSM2-GNAI confers on the first row its unique tallest identity and participates in generating differential row identity across the hair bundle.

摘要

内耳毛细胞的转导隔室,即毛束,由高度分级的静纤毛列组成,这一特性对于感觉功能至关重要,但在分子水平上仍知之甚少。我们之前的研究表明,GPSM2-GNAI 富集在静纤毛的远端尖端,对于其出生后的伸长和毛束形态发生是必需的,这两个特征与 MYO15A(短型)、WHRN 和 EPS8 蛋白共享。在这里,我们首先对小鼠听觉上皮进行了全面的遗传分析,结果表明 GPSM2、GNAI、MYO15A 和 WHRN 在同一个途径中呈串联排列。为了了解这些功能不同的蛋白质如何作为一个必需的复合物起作用,我们随后系统地分析了它们在正常和突变毛束中的分布随时间的变化。我们发现 WHRN-GPSM2-GNAI 是一个额外的模块,由预先存在的 MYO15A-EPS8 静纤毛尖端复合物招募并添加。这个扩展的复合物只存在于第一个、最高的一排,并且需要稳定比较短的一排更多的 MYO15A-EPS8,而较短的一排只含有 MYO15A-EPS8。在 GPSM2 或 GNAI 功能缺失的情况下,包括在显性的 Myo15a 和 Whrn 突变体中,毛束保留了与分子水平上的通用静纤毛相似的胚胎样组织。我们提出 GPSM2-GNAI 赋予了第一排其独特的最高身份,并参与了毛束中不同排身份的产生。

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