Department of Biology, Lund University, Lund, Sweden.
Department of Biology, Lund University, Lund, Sweden.
Mitochondrion. 2020 Jul;53:166-177. doi: 10.1016/j.mito.2020.05.009. Epub 2020 Jun 2.
Mitochondria are key components of eukaryotic cells, so their proper functioning is monitored via different mitochondrial signalling responses. One of these mitochondria-to-nuclear 'retrograde' responses to maintain mitochondrial homeostasis is the mitochondrial unfolded protein response (UPR), which can be activated by a variety of defects including blocking mitochondrial translation, respiration, protein import or transmembrane potential. Although UPR was first reported in cultured mammalian cells, this signalling pathway has also been extensively studied in the nematode Caenorhabditis elegans. In yeast, there are no published studies focusing on UPR in a strict sense, but other unfolded protein responses (UPR) that appear related to UPR have been described, such as the UPR activated by protein mistargeting (UPR) and mitochondrial compromised protein import response (mitoCPR). In plants, very little is known about UPR and only recently some of the regulators have been identified. In this paper, we summarise and compare the current knowledge of the UPR and related responses across eukaryotic kingdoms: animals, fungi and plants. Our comparison suggests that each kingdom has evolved its own specific set of regulators, however, the functional categories represented among UPR-related target genes appear to be largely overlapping. This indicates that the strategies for preserving proper mitochondrial functions are partially conserved, targeting mitochondrial chaperones, proteases, import components, dynamics and stress response, but likely also non-mitochondrial functions including growth regulators/hormone balance and amino acid metabolism. We also identify homologs of known UPR regulators and responsive genes across kingdoms, which may be interesting targets for future research.
线粒体是真核细胞的关键组成部分,因此通过不同的线粒体信号反应来监测其正常功能。其中一种维持线粒体稳态的线粒体到核的“逆行”反应是线粒体未折叠蛋白反应(UPR),它可以被多种缺陷激活,包括阻断线粒体翻译、呼吸、蛋白质输入或跨膜电位。尽管 UPR 最初是在培养的哺乳动物细胞中报道的,但这条信号通路在秀丽隐杆线虫中也得到了广泛研究。在酵母中,没有关于严格意义上的 UPR 的已发表研究,但已经描述了其他与 UPR 相关的未折叠蛋白反应(UPR),如由蛋白质靶向错误激活的 UPR 和线粒体受损蛋白质输入反应(mitoCPR)。在植物中,对 UPR 的了解甚少,直到最近才鉴定出一些调控因子。在本文中,我们总结和比较了真核生物界(动物、真菌和植物)中 UPR 和相关反应的现有知识。我们的比较表明,每个生物界都进化出了自己特定的调控因子集,然而,UPR 相关靶基因所代表的功能类别似乎在很大程度上是重叠的。这表明,保留适当的线粒体功能的策略在一定程度上是保守的,针对线粒体伴侣、蛋白酶、输入成分、动力学和应激反应,但也可能针对非线粒体功能,包括生长调节剂/激素平衡和氨基酸代谢。我们还鉴定了跨生物界的已知 UPR 调控因子和响应基因的同源物,这些可能是未来研究的有趣目标。