回顾酵母Atg1复合体的进化。

Autophagy reports Pub Date : 2025-09-29 eCollection Date: 2025-01-01 DOI:10.1080/27694127.2025.2555835
Kha M Nguyen, Hannah R Shariati, Calvin K Yip
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引用次数: 0

摘要

出芽酵母Saccharomyces cerevisiae Atg1复合体协调非选择性自噬的启动,由Atg1激酶、Atg13调节亚基和Atg17、Atg29和Atg31组成的s形支架组成。相比之下,分裂酵母Schizosaccharomyces pombe Atg1复合体包含Atg101而不是Atg29和Atg31,并且具有杆状的Atg17支架。这种分化的时间及其对Atg17结构演变的影响尚不清楚。我们的系统成分分析显示,Atg101存在于几种出芽酵母的Atg1复合体中,其中两种同时含有Atg29/Atg31和Atg101。结构建模和阴性染色电镜分析表明,含Atg101的出芽酵母呈现棒状的Atg17。此外,我们发现S. pombe的Atg13 HORMA结构域可能具有稳定帽,这表明Atg101具有替代功能。总的来说,我们的发现描绘了酵母中Atg1复合物的潜在进化轨迹。缩写:ATG,自噬相关;BLAST,基本的局部比对搜索工具;C-Mad2,闭合Mad2;早期自噬靶向/阻滞;EM,电子显微镜;组氨酸-麦芽糖结合蛋白His-MBP;HORMA, Hop1, Rev7, Mad2;IDR,本质无序区;O-Mad2,打开Mad2;交互式生命之树;PAS,噬菌体组装位点;PI3K,磷脂酰肌醇3激酶;PMSF,苯基甲基磺酰氟;pTM,预测模板建模;RMSD,均方根偏差;TOR,雷帕霉素靶;TORC1, TOR复合体1。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Revisiting the evolution of the yeast Atg1 complex.

The budding yeast Saccharomyces cerevisiae Atg1 complex coordinates the initiation of nonselective autophagy and consists of the Atg1 kinase, Atg13 regulatory subunit, and an S-shaped scaffold formed by Atg17, Atg29, and Atg31. In contrast, the fission yeast Schizosaccharomyces pombe Atg1 complex incorporates Atg101 instead of Atg29 and Atg31 and features a rod-shaped Atg17 scaffold. The timing of this divergence and its impact on the structural evolution of Atg17 remain unclear. Our systematic composition analysis revealed that Atg101 is found in the Atg1 complex of several budding yeast species, including two that contain both Atg29/Atg31 and Atg101. Structural modeling and negative stain EM analysis indicated that budding yeast species with Atg101 exhibit a rod-shaped Atg17. Additionally, we found that the Atg13 HORMA domain of S. pombe may possess a stabilizing cap, suggesting an alternative function for Atg101. Collectively, our findings delineate the potential evolutionary trajectories of the Atg1 complex in yeast. Abbreviations: ATG, autophagy-related; BLAST, basic local alignment search tool; C-Mad2, closed Mad2; EAT, Early Autophagy Targeting/Tethering; EM, electron microscopy; His-MBP, histidine-maltose binding protein; HORMA, Hop1, Rev7, and Mad2; IDR, intrinsically disordered region; O-Mad2, open Mad2; iTOL, Interactive Tree of Life; PAS, phagophore assembly site; PI3K, phosphatidylinositol 3-kinase; PMSF, phenylmethylsulfonyl fluoride; pTM, predicted template modeling; RMSD, root mean square deviation; TOR, target of rapamycin; TORC1, TOR complex 1.

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