Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders, Ministry of Education, Bio-X Institutes, Shanghai Jiao Tong University, Shanghai, 200030, China.
Shandong Provincial Key Laboratory of Animal Cell and Developmental Biology, School of Life Sciences, Shandong University, Qingdao, Shandong, 266237, China.
Nat Commun. 2023 Mar 24;14(1):1657. doi: 10.1038/s41467-023-37267-5.
Stereocilia are actin-based cell protrusions of inner ear hair cells and are indispensable for mechanotransduction. Ankle links connect the ankle region of developing stereocilia, playing an essential role in stereocilia development. WHRN, PDZD7, ADGRV1 and USH2A have been identified to form the so-called ankle link complex (ALC); however, the detailed mechanism underlying the temporal emergence and degeneration of ankle links remains elusive. Here we show that WHRN and PDZD7 orchestrate ADGRV1 and USH2A to assemble the ALC through liquid-liquid phase separation (LLPS). Disruption of the ALC multivalency for LLPS largely abolishes the distribution of WHRN at the ankle region of stereocilia. Interestingly, high concentration of ADGRV1 inhibits LLPS, providing a potential mechanism for ALC disassembly. Moreover, certain deafness mutations of ALC genes weaken the multivalent interactions of ALC and impair LLPS. In conclusion, our study demonstrates that LLPS mediates ALC formation, providing essential clues for understanding the pathogenesis of deafness.
纤毛是内耳毛细胞的肌动蛋白细胞突起,对于机械转导是不可或缺的。踝链接连接着发育中的纤毛的踝部区域,在纤毛发育中起着至关重要的作用。已经鉴定出 WHRN、PDZD7、ADGRV1 和 USH2A 形成所谓的踝链接复合物(ALC);然而,踝链接暂时出现和退化的详细机制仍然难以捉摸。在这里,我们表明 WHRN 和 PDZD7 通过液-液相分离(LLPS)协调 ADGRV1 和 USH2A 组装 ALC。破坏用于 LLPS 的踝链接多价性在很大程度上消除了 WHRN 在纤毛踝部区域的分布。有趣的是,ADGRV1 的高浓度抑制 LLPS,为 ALC 解体提供了潜在的机制。此外,ALC 基因的某些耳聋突变削弱了 ALC 的多价相互作用,并损害了 LLPS。总之,我们的研究表明 LLPS 介导了 ALC 的形成,为理解耳聋的发病机制提供了重要线索。