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A SUF Fe-S Cluster Biogenesis System in the Mitochondrion-Related Organelles of the Anaerobic Protist Pygsuia
Many microbial eukaryotes have evolved anaerobic alternatives to mitochondria known as mitochondrion-related organelles (MROs). Yet, only a few of these have been experimentally investigated. Here we report an RNA-seq-based reconstruction of the MRO proteome of Pygsuia biforma, an anaerobic represen...
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Published in: | Current biology 2014-06, Vol.24 (11), p.1176-1186 |
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Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
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Online Access: | Get full text |
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Summary: | Many microbial eukaryotes have evolved anaerobic alternatives to mitochondria known as mitochondrion-related organelles (MROs). Yet, only a few of these have been experimentally investigated. Here we report an RNA-seq-based reconstruction of the MRO proteome of Pygsuia biforma, an anaerobic representative of an unexplored deep-branching eukaryotic lineage.
Pygsuia’s MRO has a completely novel suite of functions, defying existing “function-based” organelle classifications. Most notable is the replacement of the mitochondrial iron-sulfur cluster machinery by an archaeal sulfur mobilization (SUF) system acquired via lateral gene transfer (LGT). Using immunolocalization in Pygsuia and heterologous expression in yeast, we show that the SUF system does indeed localize to the MRO. The Pygsuia MRO also possesses a unique assemblage of features, including: cardiolipin, phosphonolipid, amino acid, and fatty acid metabolism; a partial Kreb’s cycle; a reduced respiratory chain; and a laterally acquired rhodoquinone (RQ) biosynthesis enzyme. The latter observation suggests that RQ is an electron carrier of a fumarate reductase-type complex II in this MRO.
The unique functional profile of this MRO underscores the tremendous plasticity of mitochondrial function within eukaryotes and showcases the role of LGT in forging metabolic mosaics of ancestral and newly acquired organellar pathways.
•The deep-branching anaerobe Pygsuia has a unique mitochondrion-related organelle (MRO)•One hundred twenty-two proteins are predicted to localize to the MRO of Pygsuia•A SUF system has replaced the mitochondrial Fe-S cluster biosynthesis machinery•This proteome is a mosaic of ancestral and laterally transferred metabolic systems
Stairs et al. show that the proteome of the mitochondrion-related organelle of a anaerobic protist, Pygsuia biforma, is a tapestry of ancestral and laterally acquired pathways that defies organelle classification schemes. Notably, the universally conserved Fe-S cluster biosynthesis system has been replaced by an archaeal sulfur mobilization system. |
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ISSN: | 0960-9822 1879-0445 |
DOI: | 10.1016/j.cub.2014.04.033 |