Prohibitins, Phb1 and Phb2, function as Atg8 receptors to support yeast mitophagy and also play a negative regulatory role in Atg32 processing.

Autophagy Pub Date : 2024-11-01 Epub Date: 2024-07-04 DOI:10.1080/15548627.2024.2371717
Diana García-Chávez, Eunice Domínguez-Martín, Laura Kawasaki, Laura Ongay-Larios, Hilario Ruelas-Ramírez, Ariann E Mendoza-Martinez, Juan P Pardo, Soledad Funes, Roberto Coria
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Abstract

The prohibitins Phb1 and Phb2 assemble at the mitochondrial inner membrane to form a multi-dimeric complex. These scaffold proteins are highly conserved in eukaryotic cells, from yeast to mammals, and have been implicated in a variety of mitochondrial functions including aging, proliferation, and degenerative and metabolic diseases. In mammals, PHB2 regulates PINK1-PRKN mediated mitophagy by interacting with lipidated MAP1LC3B/LC3B. Despite their high conservation, prohibitins have not been linked to mitophagy in budding yeasts. In this study, we demonstrate that both Phb1 and Phb2 are required to sustain mitophagy in Saccharomyces cerevisiae. Prohibitin-dependent mitophagy requires formation of the Phb1-Phb2 complex and a conserved AIM/LIR-like motif identified in both yeast prohibitins. Furthermore, both Phb1 and Phb2 interact and exhibit mitochondrial colocalization with Atg8. Interestingly, we detected a basal C terminus processing of the mitophagy receptor Atg32 that depends on the presence of the i-AAA Yme1. In the absence of prohibitins this processing is highly enhanced but reverted by the inactivation of the rhomboid protease Pcp1. Together our results revealed a novel role of yeast prohibitins in mitophagy through its interaction with Atg8 and regulating an Atg32 proteolytic event. Abbreviation: AIM/LIR: Atg8-family interacting motif/LC3-interacting region; ANOVA: analysis of variance; ATG/Atg: autophagy related; C terminus/C-terminal: carboxyl terminus/carboxyl-terminal; GFP: green fluorescent protein; HA: human influenza hemagglutinin; Idh1: isocitrate dehydrogenase 1; MAP1C3B/LC3B: microtubule associated protein 1 light chain 3 beta; mCh: mCherry; MIM: mitochondrial inner membrane; MOM: mitochondrial outer membrane; N starvation: nitrogen starvation; N terminus: amino terminus; PARL: presenilin associated rhomboid like; Pcp1: processing of cytochrome c peroxidase 1; PCR: polymerase chain reaction; PGAM5: PGAM family member 5 mitochondrial serine/threonine protein phosphatase; PHBs/Phb: prohibitins; PINK1: PTEN induced kinase 1; PMSF: phenylmethylsulfonyl fluoride; PRKN: parkin RBR E3 ubiquitin protein ligase; SD: synthetic defined medium; SDS: sodium dodecyl sulfate; SMD-N: synthetic defined medium lacking nitrogen; WB: western blot; WT: wild type; Yme1: yeast mitochondrial escape 1; YPD: yeast extract-peptone-dextrose medium; YPLac: yeast extract-peptone-lactate medium.

抑制素 Phb1 和 Phb2 作为 Atg8 受体支持酵母的有丝分裂,并在 Atg32 处理过程中发挥负调控作用。
禁止蛋白 Phb1 和 Phb2 在线粒体内膜上组装成一个多二聚体复合物。这些支架蛋白在真核细胞(从酵母到哺乳动物)中高度保守,与线粒体的多种功能有关,包括衰老、增殖以及退行性和代谢性疾病。在哺乳动物中,PHB2 通过与脂质化的 MAP1LC3B/LC3B 相互作用,调节 PINK1-PRKN 介导的有丝分裂。尽管禁止素具有很高的保守性,但在芽殖酵母中还没有发现它们与有丝分裂有关。在这项研究中,我们证明了在酿酒酵母中维持有丝分裂需要 Phb1 和 Phb2。抑制素依赖性有丝分裂需要 Phb1-Phb2 复合物的形成以及在两种酵母抑制素中发现的类似 AIM/LIR 的保守基团。此外,Phb1和Phb2都与Atg8相互作用并表现出线粒体共定位。有趣的是,我们检测到有丝分裂受体 Atg32 的基础 C 末端处理依赖于 i-AAA Yme1 的存在。在禁用蛋白缺失的情况下,这种处理会高度增强,但如果斜方形蛋白酶 Pcp1 失活,这种处理就会恢复。总之,我们的研究结果揭示了酵母抑肽素通过与 Atg8 的相互作用和调节 Atg32 蛋白水解事件在有丝分裂过程中的新作用。缩写:AIM/LIR:Atg8-family interacting motif/LC3-interacting region;ANOVA:方差分析;ATG/Atg:自噬相关;C terminus/C-terminal:羧基末端/羧基末端;GFP:绿色荧光蛋白;HA:人流感血凝素;Idh1:mCh:mCherry;MIM:线粒体内膜;MOM:线粒体外膜;N starvation:氮饥饿;N terminus:氨基末端;PARL:presenilin associated rhomboid like;Pcp1:PCR:聚合酶链反应;PGAM5:PGAM 家族成员 5 线粒体丝氨酸/苏氨酸蛋白磷酸酶;PHBs/Phb:禁用蛋白;PINK1:PTEN 诱导激酶 1;PMSF:苯甲基磺酰氟;PRKN:Parkin RBR E3 泛素蛋白连接酶;SD:SDS:合成限定培养基;SDS:十二烷基硫酸钠;SMD-N:缺氮合成限定培养基;WB:Western 印迹;WT:野生型;Yme1:酵母线粒体逸出 1;YPD:酵母提取物-蛋白胨-葡萄糖培养基;YPLac:酵母提取物-蛋白胨-乳酸盐培养基。
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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