Departamento de Bioquímica y Biología Estructural, Instituto de Fisiología Celular, Mexico City, México.
National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.
Autophagy. 2024 Nov;20(11):2478-2489. doi: 10.1080/15548627.2024.2371717. Epub 2024 Jul 4.
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 . 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. : 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 组装在线粒体的内膜上,形成多二聚体复合物。这些支架蛋白在真核细胞中高度保守,从酵母到哺乳动物,并与各种线粒体功能有关,包括衰老、增殖以及退行性和代谢疾病。在哺乳动物中,PHB2 通过与脂化的 MAP1LC3B/LC3B 相互作用来调节 PINK1-PRKN 介导的线粒体自噬。尽管它们高度保守,但在芽殖酵母中尚未发现抑制素与线粒体自噬有关。在这项研究中,我们证明 Phb1 和 Phb2 都需要维持 的线粒体自噬。抑制素依赖性的线粒体自噬需要 Phb1-Phb2 复合物的形成,以及在酵母抑制素中鉴定的保守的 AIM/LIR 样基序。此外,Phb1 和 Phb2 都与 Atg8 相互作用,并在线粒体中共定位。有趣的是,我们检测到自噬受体 Atg32 的 C 端的基础加工,这依赖于 i-AAA Yme1 的存在。在没有抑制素的情况下,这种加工被高度增强,但通过失活 Rhomboid 蛋白酶 Pcp1 而逆转。我们的结果共同揭示了酵母抑制素通过与 Atg8 相互作用并调节 Atg32 蛋白水解事件,在线粒体自噬中的新作用。:AIM/LIR:Atg8 家族相互作用基序/LC3 相互作用区;ANOVA:方差分析;ATG/Atg:自噬相关;C 端/C-末端:羧基末端/carboxyl-terminal;GFP:绿色荧光蛋白;HA:人流感血凝素;Idh1:异柠檬酸脱氢酶 1;MAP1C3B/LC3B:微管相关蛋白 1 轻链 3β;mCh:mCherry;MIM:线粒体内膜;MOM:线粒体外膜;N 饥饿:N 饥饿;N 端:氨基末端;PARL:早老素相关的 Rhomboid 样;Pcp1:细胞色素 c 过氧化物酶 1 的加工;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:抑制素;PINK1:PTEN 诱导的激酶 1;PMSF:苯甲基磺酰氟;PRKN:Parkin RBR E3 泛素蛋白连接酶;SD:合成的定义培养基;SDS:十二烷基硫酸钠;SMD-N:缺乏氮的合成定义培养基;WB:Western blot;WT:野生型;Yme1:酵母线粒体逃逸 1;YPD:酵母提取物-胰蛋白胨-葡萄糖培养基;YPLac:酵母提取物-胰蛋白胨-乳酸培养基。