Cardiovascular and Metabolic Diseases, Duke-NUS Medical School, 169857 Singapore, Singapore.
Cardiovascular and Metabolic Diseases, Duke-NUS Medical School, 169857 Singapore, Singapore; Department of Biochemistry, Department of Cardiology of First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Cell Rep. 2022 Aug 16;40(7):111204. doi: 10.1016/j.celrep.2022.111204.
Electron transport chain (ETC) biogenesis is tightly coupled to energy levels and availability of ETC subunits. Complex III (CIII), controlling ubiquinol:ubiquinone ratio in ETC, is an attractive node for modulating ETC levels during metabolic stress. Here, we report the discovery of mammalian Co-ordinator of mitochondrial CYTB (COM) complexes that regulate the stepwise CIII biogenesis in response to nutrient and nuclear-encoded ETC subunit availability. The COMA complex, consisting of UQCC1/2 and membrane anchor C16ORF91, facilitates translation of CIII enzymatic core subunit CYTB. Subsequently, microproteins SMIM4 and BRAWNIN together with COMA subunits form the COMB complex to stabilize nascent CYTB. Finally, UQCC3-containing COMC facilitates CYTB hemylation and association with downstream CIII subunits. Furthermore, when nuclear CIII subunits are limiting, COMB is required to chaperone nascent CYTB to prevent OXPHOS collapse. Our studies highlight CYTB synthesis as a key regulatory node of ETC biogenesis and uncover the roles of microproteins in maintaining mitochondrial homeostasis.
电子传递链(ETC)的生物发生与能量水平和 ETC 亚基的可用性紧密相关。控制 ETC 中泛醌醇:泛醌比的复合物 III(CIII)是调节代谢应激期间 ETC 水平的一个有吸引力的节点。在这里,我们报告了哺乳动物线粒体 CYTB(COM)复合物协调因子的发现,该因子可响应营养物质和核编码的 ETC 亚基的可用性来调节 CIII 生物发生的逐步过程。由 UQCC1/2 和膜锚定 C16ORF91 组成的 COMA 复合物促进 CIII 酶核心亚基 CYTB 的翻译。随后,微蛋白 SMIM4 和 BRAWNIN 与 COMA 亚基一起形成 COMB 复合物以稳定新生的 CYTB。最后,含有 UQCC3 的 COMC 促进 CYTB 的血卟啉化和与下游 CIII 亚基的结合。此外,当核 CIII 亚基受到限制时,COMB 对于将新生的 CYTB 伴侣以防止 OXPHOS 崩溃是必需的。我们的研究强调了 CYTB 合成作为 ETC 生物发生的关键调节节点,并揭示了微蛋白在维持线粒体动态平衡中的作用。