The evolutionary origin of peroxisomes:: An ER-peroxisome connection

被引:125
作者
Schlüter, A
Fourcade, S
Ripp, R
Mandel, JL
Poch, O
Pujol, A [1 ]
机构
[1] Univ Strasbourg 1, Coll France, CNRS,INSERM, Inst Genet & Biol Mol & Cellulaire, Illkirch Graffenstaden, France
[2] Hosp Duran & Reynals, Inst Invest Biomed Bellvitge, Inst Recerca Oncol, Ctr Genet Med & Mol, Barcelona, Spain
[3] Inst Catalana Recerca & Estudios Avancats, Barcelona, Spain
关键词
peroxisome; endoplasmic reticulum; functional genomics; peroxisomal markers;
D O I
10.1093/molbev/msj103
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The peroxisome is an essential eukaryotic organelle, crucial for lipid metabolism and free radical detoxification, development, differentiation, and morphogenesis from yeasts to humans. Loss of peroxisomes invariably leads to fatal peroxisome biogenesis disorders in man. The evolutionary origin of peroxisomes remains unsolved; proposals for either a symbiogenetic or cellular membrane invagination event are unconclusive. To address this question, we have probed with a peroxisomal proteome, an "ensemble" of 19 representative eukaryotic complete genomes. Molecular phylogenetic and sequence comparison tools allowed us to identify four proteins as peroxisomal markers for unequivocal in silico peroxisome detection. We have then detected the Apicomplexa phylum as the first group of organisms devoid of peroxisomes, in the presence of mitochondria. Finally, we deliver evidence against a prokaryotic ancestor of peroxisomes: (1) the peroxisomal membrane is composed of purely eukaryotic bricks and is thus useful to trace the eukaryotes in their evolutionary paths and (2) the peroxisomal matrix protein import system shares mechanistic similarities with the endoplasmic reticulum/proteasome degradation process, indicating a common evolutionary history.
引用
收藏
页码:838 / 845
页数:8
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