Polarized anionic phospholipids and exocytosis are implicated in the polarized recruitment of budding yeast AP180, an endocytic initiator.

IF 2.7 3区 生物学 Q3 CELL BIOLOGY
Molecular Biology of the Cell Pub Date : 2026-06-01 Epub Date: 2026-04-08 DOI:10.1091/mbc.E24-10-0446
Paul Marchando, Gean Hu, Feng Yuan, Jordan M Ngo, Yidi Sun, David G Drubin
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引用次数: 0

Abstract

Understanding of the mechanisms that initiate clathrin-mediated endocytosis (CME) is incomplete. Recent studies in budding yeast identified the endocytic adaptor proteins Yap1801/Yap1802 (budding yeast AP180) as key CME factors that promote CME initiation in daughter cells during polarized growth, but how Yap1801/2 are recruited preferentially to the plasma membrane of daughter cells is not clear. The only known cargos for Yap1801/2 in yeast are the synaptobrevins Snc1 and Snc2, which serve as v-SNARES for exocytic vesicles reaching the plasma membrane and are crucial for polarized cell growth. In this study, we examine the spatiotemporal dynamics of functional, fluorescent protein-tagged Snc2 expressed from its endogenous locus and provide evidence that, along with anionic phospholipids, Snc2 specifically recruits Yap1802 to growing daughter cells. This protein-protein interaction creates a direct link between polarized secretion and CME and has further implications in CME initiation.

极化阴离子磷脂和胞吐作用与芽殖酵母AP180(一种内吞引发剂)的极化招募有关。
对发起网格蛋白介导的内吞作用(CME)的机制的了解尚不完整。最近对出芽酵母的研究发现,在子代细胞极化生长过程中,胞内吞噬衔接蛋白Yap1801/Yap1802(出芽酵母AP180)是促进子代细胞发生CME的关键因子,但目前尚不清楚Yap1801/2是如何优先被募集到子代细胞的质膜上的。酵母中唯一已知的Yap1801/2的载体是突触蛋白Snc1和Snc2,它们作为胞外囊泡到达质膜的v-SNARES,对极化细胞生长至关重要。在这项研究中,我们研究了功能性荧光蛋白标记的Snc2从其内源性位点表达的时空动态,并提供证据表明,Snc2与阴离子磷脂一起,特异性地招募Yap1802生长子细胞。这种蛋白-蛋白相互作用在极化分泌和CME之间建立了直接联系,并对CME的发生有进一步的影响。[媒体:见文][媒体:见文]。
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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来源期刊
Molecular Biology of the Cell
Molecular Biology of the Cell 生物-细胞生物学
CiteScore
6.00
自引率
6.10%
发文量
402
审稿时长
2 months
期刊介绍: MBoC publishes research articles that present conceptual advances of broad interest and significance within all areas of cell, molecular, and developmental biology. We welcome manuscripts that describe advances with applications across topics including but not limited to: cell growth and division; nuclear and cytoskeletal processes; membrane trafficking and autophagy; organelle biology; quantitative cell biology; physical cell biology and mechanobiology; cell signaling; stem cell biology and development; cancer biology; cellular immunology and microbial pathogenesis; cellular neurobiology; prokaryotic cell biology; and cell biology of disease.
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