Gabaldón Toni
Centre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology (BIST), Dr. Aiguader, 88, 08003, Barcelona, Spain.
Universitat Pompeu Fabra (UPF), 08003, Barcelona, Spain.
Subcell Biochem. 2018;89:221-233. doi: 10.1007/978-981-13-2233-4_9.
Peroxisomes are single-membrane bound intracellular organelles that can be found in organisms across the tree of eukaryotes, and thus are likely to derive from an ancestral peroxisome in the last eukaryotic common ancestor (LECA). Yet, peroxisomes in different lineages can present a large diversity in terms of their metabolic capabilities, which reflects a highly variable proteomic content. Theories on the evolutionary origin of peroxisomes have shifted in the last decades from scenarios involving an endosymbiotic origin, similar to those of mitochondria and plastids, towards hypotheses purporting an endogenous origin from within the endomembrane system. The peroxisomal proteome is highly dynamic in evolutionary terms, and can evolve via differential loss and gain of proteins, as well as via relocalization of proteins from and to other sub-cellular compartments. Here, I review current knowledge and discussions on the diversity, origin, and evolution of the peroxisomal proteome.
过氧化物酶体是一种被单层膜包裹的细胞内细胞器,存在于整个真核生物界的生物体中,因此很可能起源于最后一个真核生物共同祖先(LECA)中的原始过氧化物酶体。然而,不同谱系中的过氧化物酶体在代谢能力方面可能存在很大差异,这反映了其蛋白质组含量的高度变异性。在过去几十年里,关于过氧化物酶体进化起源的理论已从涉及内共生起源(类似于线粒体和质体的起源)的设想,转向主张其起源于内膜系统内部的内源性起源假说。从进化角度来看,过氧化物酶体蛋白质组具有高度动态性,它可以通过蛋白质的差异丢失和获得,以及蛋白质在其他亚细胞区室之间的重新定位来进化。在此,我综述了关于过氧化物酶体蛋白质组的多样性、起源和进化的当前知识及相关讨论。