内体
逆转体
生物
细胞生物学
高尔基体
分泌物
Wnt信号通路
转运蛋白
信号转导
生物化学
内质网
细胞内
作者
Hilal Ahmad Reshi,Raghavender Medishetti,Aishwarya Ahuja,Deepa Balasubramanian,Kavita Babu,Manish Jaiswal,Kiranam Chatti,Subbareddy Maddika
标识
DOI:10.1016/j.devcel.2024.05.021
摘要
Retrograde transport of WLS (Wntless) from endosomes to trans-Golgi network (TGN) is required for efficient Wnt secretion during development. However, the molecular players connecting endosomes to TGN during WLS trafficking are limited. Here, we identified a role for Eyes Absent (EYA) proteins during retrograde trafficking of WLS to TGN in human cell lines. By using worm, fly, and zebrafish models, we found that the EYA-secretory carrier-associated membrane protein 3 (SCAMP3) axis is evolved in vertebrates. EYAs form a complex and interact with retromer on early endosomes. Retromer-bound EYA complex recruits SCAMP3 to endosomes, which is necessary for the fusion of WLS-containing endosomes to TGN. Loss of EYA complex or SCAMP3 leads to defective transport of WLS to TGN and failed Wnt secretion. EYA mutations found in patients with hearing loss form a dysfunctional EYA-retromer complex that fails to activate Wnt signaling. These findings identify the EYA complex as a component of retrograde trafficking of WLS from the endosome to TGN.
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