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Minimal cytosolic iron‐sulfur cluster assembly machinery of Giardia intestinalis is partially associated with mitosomes
Author(s) -
Pyrih Jan,
Pyrihová Eva,
Kolísko Martin,
Stojanovová Darja,
Basu Somsuvro,
Harant Karel,
Haindrich Alexander C.,
Doležal Pavel,
Lukeš Julius,
Roger Andrew,
Tachezy Jan
Publication year - 2016
Publication title -
molecular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.857
H-Index - 247
eISSN - 1365-2958
pISSN - 0950-382X
DOI - 10.1111/mmi.13487
Subject(s) - biology , cytosol , organelle , mitochondrion , iron–sulfur cluster , microbiology and biotechnology , giardia , genome , function (biology) , biochemistry , computational biology , genetics , gene , enzyme
Summary Iron‐sulfur (Fe‐S) clusters are essential cofactors that enable proteins to transport electrons, sense signals, or catalyze chemical reactions. The maturation of dozens of Fe‐S proteins in various compartments of every eukaryotic cell is driven by several assembly pathways. The ubiquitous cytosolic Fe‐S cluster assembly (CIA) pathway, typically composed of eight highly conserved proteins, depends on mitochondrial Fe‐S cluster assembly (ISC) machinery. Giardia intestinalis contains one of the smallest eukaryotic genomes and the mitosome, an extremely reduced mitochondrion. Because the only pathway known to be retained within this organelle is the synthesis of Fe‐S clusters mediated by ISC machinery, a likely function of the mitosome is to cooperate with the CIA pathway. We investigated the cellular localization of CIA components in G. intestinalis and the origin and distribution of CIA‐related components and Tah18‐like proteins in other Metamonada. We show that orthologs of Tah18 and Dre2 are missing in these eukaryotes. In Giardia , all CIA components are exclusively cytosolic, with the important exception of Cia2 and two Nbp35 paralogs, which are present in the mitosomes. We propose that the dual localization of Cia2 and Nbp35 proteins in Giardia might represent a novel connection between the ISC and the CIA pathways.