EPG-5 regulates TGFB/TGF-β and WNT signalling by modulating retrograde endocytic trafficking.

Chongzhen Yuan, Huachuan Dong, Chunyan Wu, Jinyang Liu, Zheng Wang, Xingwei Wang, Haiyan Ren, Zhaoyu Wang, Qun Lu
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Abstract

The Vici syndrome protein EPG5 acts as a tethering factor determining the fusion specificity of autophagosomes with late endosomes/lysosomes. Here we demonstrated that during C. elegans development, EPG-5 modulates SMA and MAB TGFB/TGF-β signaling in controlling body size and also WNT signaling in regulating cell migration. EPG-5 is required for retrograde trafficking of the TGFB receptor SMA-6 and WLS/Wntless homolog MIG-14. In epg-5 mutants, SMA-6 and MIG-14 are trapped within hybrid endosomal structures, which colocalize with SNX-1- and SNX-3-labeled vesicles, respectively. Basolateral recycling processes of transmembrane cargos H.s.TFR/hTfR and H.s.IL2RA/hTAC are also defective in epg-5 mutants. Depletion of EPG-5 causes defective RAB-5 and RAB-7, and RAB-5 and RAB-10 conversion, leading to the formation of these hybrid vesicles. The defects in endocytic trafficking and autophagy in epg-5 mutants are ameliorated by knocking down components of the HOPS complex. Our study demonstrates the intersection between the autophagy pathway and the endocytic pathway, providing insights into the pathogenesis of amyotrophic lateral sclerosis (ALS) and Vici syndrome.Abbreviations: ALM: anterior lateral microtubule; ATG: autophagy related; AVM: anterior ventral microtubule; CORVET: class C core vacuole/endosome tethering; DAF-4: abnormal dauer formation 4; DIC: differential interference contrast; EPG: ectopic PGL granules; EPG-5: ectopic P granules 5; GAP: GTPase activating protein; GFP: green fluorescent protein; HOPS: homotypic fusion and vacuole protein sorting; H.s.IL2RA/hTAC: human interleukin 2 receptor subunit alpha; H.s.TFR/hTfR: human transferrin receptor; L1/L4: the first/fourth larval; mCh: mCherry; MIG-14: abnormal cell migration 14; PLM: posterior lateral microtubule; PVM: posterior ventral microtubule; RAB: ras-related protein; RFP: red fluorescent protein; RME-1: receptor mediated endocytosis 1; SMA-6: small 6; SNARE: soluble N-ethylmaleimide-sensitive factor attachment protein receptor; SNX: sorting nexin; TBC-2: TBC1 (Tre-2/Bub2/Cdc16) domain family 2; TGFB/TGF-β: transforming growth factor beta; TGN: trans-Golgi network; VPS: related to yeast vacuolar protein sorting factor; WT: wild type.

EPG-5通过调节逆行内吞运输调节tgfb/tgf-β和WNT信号。
维氏综合征蛋白EPG5是一种系留因子,决定着自噬体与晚期内体/溶酶体融合的特异性。在这里,我们证明了在秀丽隐杆线虫的发育过程中,EPG-5 可调节 SMA 和 MAB TGFB/TGF-β 信号,从而控制体型,还可调节 WNT 信号,从而调节细胞迁移。TGFB受体SMA-6和WLS/Wntless同源物MIG-14的逆向运输需要EPG-5。在epg-5突变体中,SMA-6和MIG-14被困在混合内体结构中,它们分别与SNX-1和SNX-3标记的囊泡共聚焦。在epg-5突变体中,跨膜载体H.s.TFR/hTfR和H.s.IL2RA/hTAC的基底侧再循环过程也存在缺陷。EPG-5 的缺失会导致 RAB-5 和 RAB-7 以及 RAB-5 和 RAB-10 转换的缺陷,从而形成这些混合囊泡。通过敲除 HOPS 复合物的成分,epg-5 突变体的内吞转和自噬缺陷得到了改善。我们的研究证明了自噬途径与内吞途径之间的交叉,为肌萎缩性脊髓侧索硬化症(ALS)和维氏综合征的发病机制提供了启示。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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