Abstract
Mitosomes are simple, mitochondrion-derived organelles, which were recently found in various “amitochondrial” protists, including the human parasites Entamoeba histolytica, Giardia intestinalis, Cryptosporidium parvum, and microsporidians. Similar organelles might also be present in some free-living protists. Although all these organisms underwent different evolutionary histories, they arrived at common life strategies for which oxygen-dependent ATP synthesis is not required: they inhabit either an oxygen-poor environment, such as the intestinal tract of their hosts, or they are adapted to intracellular parasitism. Consequently, the majority of their mitochondrial functions were permanently lost with concomitant loss of the organellar genome, and mitochondria gradually transformed into their highly reduced forms named mitosomes. The common features of mitosomes, which were retained and pointed to their mitochondrial origin, are a double membrane surrounding the organellar matrix, conserved mechanisms of protein import and processing, and the biosynthesis of iron–sulfur (FeS) clusters. Finding the latter function in mitosomes supports the notion that FeS cluster assembly is the only essential function of mitochondria necessary for the maturation of cellular FeS proteins. Only in the mitosomes of E. histolytica was the mitochondrion type of FeS cluster assembly machinery not conserved, and their function remains enigmatic. Unlike hydrogenosomes, another type of mitochondrion-derived organelle, mitosomes do not synthesize ATP and hydrogen. Many more investigations are required to elucidate the biology of mitosomes and the evolutionary paths leading to the formation of the various mitochondrion-derived organelles, of which mitosomes are the most simplified.
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References
Abrahamsen MS, Templeton TJ, Enomoto S, Abrahante JE, Zhu G, Lancto CA, Deng M, Liu C, Widmer G, Tzipori S, Buck GA, Xu P, Bankier AT, Dear PH, Konfortov BA, Spriggs HF, Iyer L, Anantharaman V, Aravind L, Kapur V (2004) Complete genome sequence of the apicomplexan, Cryptosporidium parvum. Science 304:441–445
Adam RD (2001) Biology of Giardia lamblia. Clin Microbiol Rev 14:447–475
Adams KL, Palmer JD (2003) Evolution of mitochondrial gene content: gene loss and transfer to the nucleus. Mol Phylogenet Evol 29:380–395
Agar JN, Yuvaniyama P, Jack RF, Cash VL, Smith AD, Dean DR, Johnson MK (2000) Modular organization and identification of a mononuclear iron-binding site within the NifU protein. J Biol Inorg Chem 5:167–177
Ali V, Shigeta Y, Tokumoto U, Takahashi Y, Nozaki T (2004) An intestinal parasitic protist, Entamoeba histolytica, possesses a non-redundant nitrogen fixation-like system for iron–sulfur cluster assembly under anaerobic conditions. J Biol Chem 279:16863–16874
Alves R, Herrero E, Sorribas A (2004) Predictive reconstruction of the mitochondrial iron–sulfur cluster assembly metabolism. II. Role of glutaredoxin Grx5. Proteins Struct Funct Bioinf 57:481–492
Andersson JO, Sjogren AM, Horner DS, Murphy CA, Dyal PL, Svard SG, Logsdon JM Jr, Ragan MA, Hirt RP, Roger AJ (2007) A genomic survey of the fish parasite Spironucleus salmonicida indicates genomic plasticity among diplomonads and significant lateral gene transfer in eukaryote genome evolution. BMC Genomics 8:51
Arisue N, Sánchez LB, Weiss LM, Müller M, Hashimoto T (2002) Mitochondrial-type Hsp70 genes of the amitochondriate protists, Giardia intestinalis, Entamoeba histolytica and two microsporidians. Parasitol Int 51:9–16
Balk J, Aguilar Netz DJ, Tepper K, Pierik AJ, Lill R (2005a) The essential WD40 protein Cia1 is involved in a late step of cytosolic and nuclear iron–sulfur protein assembly. Mol Cell Biol 25:10833–10841
Balk J, Pierik AJ, Aguilar Netz DJ, Mühlenhoff U, Lill R (2005b) Nar1p, a conserved eukaryotic protein with similarity to Fe-only hydrogenases, functions in cytosolic iron–sulphur protein biogenesis. Biochem Soc Trans 33:86–89
Benchimol M (2007) Structure of the Hydrogenosomes (in this volume). Springer, Heidelberg
Bernas T, Dobrucki JW (2000) The role of plasma membrane in bioreduction of two tetrazolium salts, MTT, and CTC. Arch Biochem Biophys 380:108–116
Best AA, Morrison HG, McArthur AG, Sogin ML, Olsen GJ (2004) Evolution of eukaryotic transcription: insights from the genome of Giardia lamblia. Genome Res 14:1537–1547
Boldogh IR, Fehrenbacher KL, Yang HC, Pon LA (2005) Mitochondrial movement and inheritance in budding yeast. Gene 354:28–36
Breeuwer P, Abee T (2000) Assessment of viability of microorganisms employing fluorescence techniques. Int J Food Microbiol 55:193–200
Brown DM, Upcroft JA, Upcroft P (1993) Cysteine is the major low molecular weight thiol in Giardia duodenalis. Mol Biochem Parasitol 61:155–158
Bui ET, Bradley PJ, Johnson PJ (1996) A common evolutionary origin for mitochondria and hydrogenosomes. Proc Natl Acad Sci USA 93:9651–9656
Burri L, Williams BA, Bursac D, Lithgow T, Keeling PJ (2006) Microsporidian mitosomes retain elements of the general mitochondrial targeting system. Proc Natl Acad Sci USA 103:15916–15920
Campuzano V, Montermini L, Molto MD, Pianese L, Cossee M, Cavalcanti F, Monros E, Rodius F, Duclos F, Monticelli A, Zara F, Canizares J, Koutnikova H, Bidichandani SI, Gellera C, Brice A, Trouillas P, DeMichele G, Filla A, DeFrutos R, Palau F, Patel PI, DiDonato S, Mandel JL, Cocozza S, Koenig M, Pandolfo M (1996) Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion. Science 271:1423–1427
Cavalier-Smith T (1987a) The origin of eukaryotic and archaebacterial cells. Ann NY Acad Sci 503:17–54
Cavalier-Smith T (1987b) Eukaryotes with no mitochondria. Nature 326:332–333
Chan KW, Slotboom DJ, Cox S, Embley TM, Fabre O, van der Giezen M, Harding M, Horner DS, Kunji ERS, Leon-Avila G, Tovar J (2005) A novel ADP/ATP transporter in the mitosome of the microaerophilic human parasite Entamoeba histolytica. Curr Biol 15:737–742
Chanez AL, Hehl AB, Engstler M, Schneider A (2006) Ablation of the single dynamin of T. brucei blocks mitochondrial fission and endocytosis and leads to a precise cytokinesis arrest. J Cell Sci 119:2968–2974
Clark CG, Roger AJ (1995) Direct evidence for secondary loss of mitochondria in Entamoeba histolytica. Proc Natl Acad Sci USA 92:6518–6521
Clayton CE, Michels P (1996) Metabolic compartmentation in African trypanosomes. Parasitol Today 12:465–471
Doležal P, Šmíd O, Rada P, Zubáčová Z, Bursac D, Šut'ák R, Nebesářová J, Lithgow T, Tachezy J (2005) Giardia mitosomes and trichomonad hydrogenosomes share a common mode of protein targeting. Proc Natl Acad Sci USA 102:10924–10929
Dutkiewicz R, Schilke B, Knieszner H, Walter W, Craig EA, Marszalek J (2003) Ssq1, a mitochondrial Hsp70 involved in iron–sulfur (Fe/S) center biogenesis: similarities to and differences from its bacterial counterpart. J Biol Chem 278:29719–29727
Dyall S, Doležal P (2007) Protein Import into Hydrogenosomes and Mitosomes (in this volume). Springer, Heidelberg
Ellis JE, Williams R, Cole D, Cammack R, Lloyd D (1993) Electron transport components of the parasitic protozoon Giardia lamblia. FEBS Lett 325:196–200
Embley TM, Finlay BJ, Dyal PL, Hirt RP, Wilkinson M, Williams AG (1995) Multiple origins of anaerobic ciliates with hydrogenosomes within the radiation of aerobic ciliates. Proc R Soc Lond B Biol Sci 262:87–93
Emelyanov VV (2003) Phylogenetic affinity of a Giardia lamblia cysteine desulfurase conforms to canonical pattern of mitochondrial ancestry. FEMS Microbiol Lett 226:257–266
Errington J, Daniel RA, Scheffers DJ (2003) Cytokinesis in bacteria. Microbiol Mol Biol Rev 67:52–65
Fry M, Beesley JE (1991) Mitochondria of mammalian Plasmodium spp. Parasitology 102:17–26
Gerber J, Mühlenhoff U, Lill R (2003) An interaction between frataxin and Isu1/Nfs1 that is crucial for Fe/S cluster synthesis on Isu1. EMBO Rep 4:906–911
Germot A, Philippe H, LeGuyader H (1996) Presence of a mitochondrial-type 70-kDa heat shock protein in Trichomonas vaginalis suggests a very early mitochondrial endosymbiosis in eukaryotes. Proc Natl Acad Sci USA 93:14614–14617
Germot A, Philippe H, LeGuyader H (1997) Evidence for loss of mitochondria in Microsporidia from a mitochondrial-type HSP70 in Nosema locustae. Mol Biochem Parasitol 87:159–168
Ghosh S, Field J, Rogers R, Hickman M, Samuelson J (2000) The Entamoeba histolytica mitochondrion-derived organelle (crypton) contains double-stranded DNA and appears to be bound by a double membrane. Infect Immun 68:4319–4322
Hampl V, Simpson AGB (2007) Possible Mitochondria-Related Organelles in Poorly-Studied “Amitochondriate” Eukaryotes (in this volume). Springer, Heidelberg
Harlow DR, Weinbach EC, Diamond LS (1976) Nicotinamide nucleotide transhydrogenase in Entamoeba histolytica, a protozoan lacking mitochondria. Comp Biochem Physiol 53:141–144
Hashimoto T (1998) Secondary absence of mitochondria in Giardia lamblia and Trichomonas vaginalis revealed by valyl-tRNA synthetase phylogeny. Proc Natl Acad Sci USA 95:6860–6865
Hatefi Y, Yamaguchi M (1996) Nicotinamide nucleotide transhydrogenase: a model for utilization of substrate binding energy for proton translocation. FASEB J 10:444–452
Hausmann A, Aguilar Netz DJ, Balk J, Pierik AJ, Mühlenhoff U, Lill R (2005) The eukaryotic P loop NTPase Nbp35: an essential component of the cytosolic and nuclear iron–sulfur protein assembly machinery. Proc Natl Acad Sci USA 102:3266–3271
Hirt RP, Logsdon JM, Healy B, Dorey MW, Doolittle WF, Embley TM (1999) Microsporidia are related to Fungi: evidence from the largest subunit of RNA polymerase II and other proteins. Proc Natl Acad Sci USA 96:580–585
Horner DS, Hirt RP, Kilvington S, Lloyd D, Embley TM (1996) Molecular data suggest an early acquisition of the mitochondrion endosymbiont. Proc R Soc Lond B Biol Sci 263:1053–1059
Horner DS, Foster PG, Embley TM (2000) Iron hydrogenases and the evolution of anaerobic eukaryotes. Mol Biol Evol 17:1695–1709
Hrdý I, Tachezy J, Müller M (2007) Metabolism of Trichomonad Hydrogenosomes (in this volume). Springer, Heidelberg
Johnson D, Dean D (2004) Structure, function, and formation of biological iron–sulfur clusters. Annu Rev Biochem 74:247–281
Katinka MD, Duprat S, Cornillot E, Metenier G, Thomarat F, Prensier G, Barbe V, Peyretaillade E, Brottier P, Wincker P, Delbac F, El Alaoui H, Peyret P, Saurin W, Gouy M, Weissenbach J, Vivares CP (2001) Genome sequence and gene compaction of the eukaryote parasite Encephalitozoon cuniculi. Nature 414:450–453
Keeling PJ, Doolittle WF (1996) Alpha-tubulin from early-diverging eukaryotic lineages and the evolution of the tubulin family. Mol Biol Evol 13:1297–1305
Keithly JS (2007) The Mitochondrion-Related Organelle of Cryptosporidium parvum (in this volume). Springer, Heidelberg
Keithly JS, Langreth SG, Buttle KF, Mannella CA (2005) Electron tomographic and ultrastructural analysis of the Cryptosporidium parvum relict mitochondrion, its associated membranes, and organelles. J Eukaryot Microbiol 52:132–140
Kennedy C, Dean D (1992) The nifU, nifS and nifV gene products are required for activity of all three nitrogenases of Azotobacter vinelandii. Mol Gen Genet 231:494–498
Kispal G, Csere P, Prohl C, Lill R (1999) The mitochondrial proteins Atm1p and Nfs1p are essential for biogenesis of cytosolic Fe/S proteins. EMBO J 18:3981–3989
Komuniecki PR, Johnson J, Kamhawi M, Komuniecki R (1993) Mitochondrial heterogeneity in the parasitic nematode, Ascaris suum. Exp Parasitol 76:424–437
Kuroiwa T, Nishida K, Yoshida Y, Fujiwara T, Mori T, Kuroiwa H, Misumi O (2006) Structure, function and evolution of the mitochondrial division apparatus. Biochim Biophys Acta 1763:510–521
LaGier MJ, Tachezy J, Stejskal F, Kutišová K, Keithly JS (2003) Mitochondrial-type iron–sulfur cluster biosynthesis genes (IscS and IscU) in the apicomplexan Cryptosporidium parvum. Microbiol-SGM 149:3519–3530
Lang BF, Burger G, O'Kelly CJ, Cedergren R, Golding GB, Lemieux C, Sankoff D, Turmel M, Gray MW (1997) An ancestral mitochondrial DNA resembling a eubacterial genome in miniature. Nature 387:493–497
Lange H, Lisowsky T, Gerber J, Mühlenhoff U, Kispal G, Lill R (2001) An essential function of the mitochondrial sulfhydryl oxidase Erv1p/ALR in the maturation of cytosolic Fe/S proteins. EMBO Rep 2:715–720
Leon-Avila G, Tovar J (2004) Mitosomes of Entamoeba histolytica are abundant mitochondrion-related remnant organelles that lack a detectable organellar genome. Microbiol-SGM 150:1245–1250
Li J, Kogan M, Knight SA, Pain D, Dancis A (1999) Yeast mitochondrial protein, Nfs1p, coordinately regulates iron–sulfur cluster proteins, cellular iron uptake, and iron distribution. J Biol Chem 274:33025–33034
Lill R, Mühlenhoff U (2006) Iron–sulfur protein biogenesis in eukaryotes: components and mechanisms. Annu Rev Cell Dev Biol 22:457–486
Lill R, Diekert K, Kaut A, Lange H, Pelzer W, Prohl C, Kispal G (1999) The essential role of mitochondria in the biogenesis of cellular iron–sulfur proteins. Biol Chem 380:1157–1166
Lindmark DG (1980) Energy metabolism of the anaerobic protozoon Giardia lamblia. Mol Biochem Parasitol 1:1–12
Lloyd D, Ralphs JR, Harris JC (2002) Giardia intestinalis, a eukaryote without hydrogenosomes, produces hydrogen. Microbiol-SGM 148:727–733
Mai Z, Ghosh S, Frisardi M, Rosenthal B, Rogers R, Samuelson J (1999) Hsp60 is targeted to a cryptic mitochondrion-derived organelle (crypton) in the microaerophilic protozoan parasite Entamoeba histolytica. Mol Cell Biol 19:2198–2205
Martin W (2007) Anaerobic Eukaryotes in Pursuit of Phylogenetic Normality: the Evolution of Hydrogenosomes and Mitosomes. Springer, Heidelberg
Martin W, Müller M (1998) The hydrogen hypothesis for the first eukaryote. Nature 392:37–41
Mercer NA, McKelvey JR, Fioravanti CF (1999) Hymenolepis diminuta: catalysis of transmembrane proton translocation by mitochondrial NADPH→NAD transhydrogenase. Exp Parasitol 91:52–58
Morrison HG, Roger AJ, Nystul TG, Gillin FD, Sogin ML (2001) Giardia lamblia expresses a proteobacterial-like DnaK homolog. Mol Biol Evol 18:530–541
Netz DJA, Pierik AJ, Stuempfig M, Mühlenhoff U, Lill R (2007) The Cfd1-Nbp35 complex acts as a scaffold for iron–sulfur protein assembly in the yeast cytosol. Nat Chem Biol 3:278–286
Nixon JEJ, Wang A, Morrison HG, McArthur AG, Sogin ML, Loftus BJ, Samuelson J (2002) A spliceosomal intron in Giardia lamblia. Proc Natl Acad Sci USA 99:3701–3705
Nohýnková E, Tùmová P, Kulda J (2006) Cell division of Giardia intestinalis: flagellar developmental cycle involves transformation and exchange of flagella between mastigonts of a diplomonad cell. Eukaryot Cell 5:753–761
Ogbadoyi EO, Robinson DR, Gull K (2003) A high-order trans-membrane structural linkage is responsible for mitochondrial genome positioning and segregation by flagellar basal bodies in trypanosomes. Mol Biol Cell 14:1769–1779
Ollagnier-de-Choudens S, Mattioli T, Tagahashi Y, Fontecave M (2001) Iron–sulfur cluster assembly: characterization of IscA and evidence for a specific and functional complex with ferredoxin. J Biol Chem 276:22604–22607
Olson JW, Agar JN, Johnson MK, Maier RJ (2000) Characterization of the NifU and NifS Fe–S cluster formation proteins essential for viability in Helicobacter pylori. Biochemistry 39:16213–16219
Orozco E, Baez-Camargo M, Riveron AM, Gharibeh R, Gariglio P, de la Cruz HF, Chavez P (1997) A model for unscheduled DNA replication in Entamoeba histolytica trophozoites. Arch Med Res 28:24–26
Putignani L, Tait A, Smith HV, Horner D, Tovar J, Tetley L, Wastling JM (2004) Characterization of a mitochondrion-like organelle in Cryptosporidium parvum. Parasitology 129:1–18
Reeves RE, Warren LG, Susskind B, Lo H-S (1977) An energy-conserving pyruvate-to-acetate pathway in Entamoeba histolytica. Pyruvate synthase and a new acetate thiokinase. J Biol Chem 252:726–731
Regoes A, Zourmpanou D, Leon-Avila G, van der Giezen M, Tovar J, Hehl AB (2005) Protein import, replication and inheritance of a vestigial mitochondrion. J Biol Chem 280:30557–30563
Riordan CE, Langreth SG, Sanchez LB, Kayser O, Keithly JS (1999) Preliminary evidence for a mitochondrion in Cryptosporidium parvum: phylogenetic and therapeutic implications. J Eukaryot Microbiol 46:52S–55S
Riordan CE, Ault JG, Langreth SG, Keithly JS (2003) Cryptosporidium parvum Cpn60 targets a relict organelle. Curr Genet 44:138–147
Rodriguez MA, Garcia-Perez RM, Mendoza L, Sanchez T, Guillen N, Orozco E (1998) The pyruvate:ferredoxin oxidoreductase enzyme is located in the plasma membrane and in a cytoplasmic structure in Entamoeba. Microb Pathog 25:1–10
Rodriguez-Manzaneque MT, Tamarit J, Belli G, Ros J, Herrero E (2002) Grx5 is a mitochondrial glutaredoxin required for the activity of iron/sulfur enzymes. Mol Biol Cell 13:1109–1121
Roger AJ, Svard SG, Tovar J, Clark CG, Smith MW, Gillin FD, Sogin ML (1998) A mitochondrial-like chaperonin 60 gene in Giardia lamblia: evidence that diplomonads once harbored an endosymbiont related to the progenitor of mitochondria. Proc Natl Acad Sci USA 95:229–234
Rouault TA, Tong WH (2005) Iron–sulphur cluster biogenesis and mitochondrial iron homeostasis. Nat Rev Mol Cell Biol 6:345–351
Roy A, Solodovnikova N, Nicholson T, Antholine W, Walden WE (2003) A novel eukaryotic factor for cytosolic Fe–S cluster assembly. EMBO J 22:4826–4835
Schilke B, Voisine C, Beinert H, Craig E (1999) Evidence for a conserved system for iron metabolism in the mitochondria of Saccharomyces cerevisiae. Proc Natl Acad Sci USA 96:10206–10211
Schwartz CJ, Djaman O, Imlay JA, Kiley PJ (2000) The cysteine desulfurase, IscS, has a major role in in vivo Fe–S cluster formation in Escherichia coli. Proc Natl Acad Sci USA 97:9009–9014
Shan Y, Napoli E, Cortopassi G (2007) Mitochondrial frataxin interacts with ISD11 of the NFS1/ISCU complex and multiple mitochondrial chaperones. Hum Mol Genet 16:929–941
Sipos K, Lange H, Fekete Z, Ullmann P, Lill R, Kispal G (2002) Maturation of cytosolic iron–sulfur proteins requires glutathione. J Biol Chem 277:26944–26949
Šlapeta J, Keithly JS (2004) Cryptosporidium parvum mitochondrial-type HSP70 targets homologous and heterologous mitochondria. Eukaryot Cell 3:483–494
Šmíd O, Horáková E, Vilímová V, Hrdý I, Cammack R, Horvath A, Lukeš J, Tachezy J (2006) Knock-downs of iron–sulfur cluster assembly proteins IscS and IscU down-regulate the active mitochondrion of procyclic Trypanosoma brucei. J Biol Chem 281:28679–28686
Sogin ML (1991) Early evolution and the origin of eukaryotes. Curr Biol 1:457–463
Stejskal F, Šlapeta J, Čtrnáctá V, Keithly JS (2003) A Narf-like gene from Cryptosporidium parvum resembles homologues observed in aerobic protists and higher eukaryotes. FEMS Microbiol Lett 229:91–96
Striepen B, Crawford MJ, Shaw MK, Tilney LG, Seeber F, Roos DS (2000) The plastid of Toxoplasma gondii is divided by association with the centrosomes. J Cell Biol 151:1423–1434
Tachezy J, Doležal P (2007) Iron–sulfur proteins and iron–sulfur cluster assembly in organisms with hydrogenosomes and mitosomes. In: Martin W, Müller M (eds) Origin of mitochondria and hydrogenosomes. Springer, Heidelberg, pp 105–133
Tachezy J, Sánchez LB, Müller M (2001) Mitochondrial type iron–sulfur cluster assembly in the amitochondriate eukaryotes Trichomonas vaginalis and Giardia intestinalis, as indicated by the phylogeny of IscS. Mol Biol Evol 18:1919–1928
Takahashi Y, Tokumoto U (2002) A third bacterial system for the assembly of iron–sulfur clusters with homologs in archaea and plastids. J Biol Chem 277:28380–28383
Tong WH, Rouault T (2000) Distinct iron–sulfur cluster assembly complexes exist in the cytosol and mitochondria of human cells. EMBO J 19:5692–5700
Tong WH, Rouault TA (2006) Functions of mitochondrial ISCU and cytosolic ISCU in mammalian iron–sulfur cluster biogenesis and iron homeostasis. Cell Metab 3:199–210
Tovar J, Fischer A, Clark CG (1999) The mitosome, a novel organelle related to mitochondria in the amitochondrial parasite Entamoeba histolytica. Mol Microbiol 32:1013–1021
Tovar J, Leon-Avila G, Sánchez LB, Sutak R, Tachezy J, van der Giezen M, Hernandez M, Müller M, Lucocq JM (2003) Mitochondrial remnant organelles of Giardia function in iron–sulphur protein maturation. Nature 426:172–176
van der Giezen M, Cox S, Tovar J (2004) The iron–sulfur cluster assembly genes iscS and iscU of Entamoeba histolytica were acquired by horizontal gene transfer. BMC Evol Biol 4:7
van Dooren GG, Marti M, Tonkin CJ, Stimmler LM, Cowman AF, McFadden GI (2005) Development of the endoplasmic reticulum, mitochondrion and apicoplast during the asexual life cycle of Plasmodium falciparum. Mol Microbiol 57:405–419
van Dooren GG, Stimmler LM, McFadden GI (2006) Metabolic maps and functions of the Plasmodium mitochondrion. FEMS Microbiol Rev 30:596–630
Vávra J (1976) Structure of the microsporidia. In: Bulla LA Jr, Cheng TS (eds) Comparative pathobiology, vol 1. Biology of the Microsporidia. Plenum, New York, pp 1–86
Vávra J (2005) Polar vesicles of microsporidia are mitochondrial remnants (mitosomes)? Folia Parasitol 52:193–195
Vickerman K (1985) Development cycles and biology of pathogenic trypanosomes. Br Med Bull 41:105–114
Wiedemann N, Frazier AE, Pfanner N (2004) The protein import machinery of mitochondria. J Biol Chem 279:14473–14476
Williams BAP, Hirt RP, Lucocq JM, Embley TM (2002) A mitochondrial remnant in the microsporidian Trachipleistophora hominis. Nature 418:865–869
Wilson RJ, Williamson DH (1997) Extrachromosomal DNA in the Apicomplexa. Microbiol Mol Biol Rev 61:1–16
Wilson RJM, Rangachari K, Saldanha JW, Rickman L, Buxton RS, Eccleston JF (2003) Parasite plastids: maintenance and functions. Philos Trans R Soc Lond B Biol Sci 358:155–162
Wu SP, Wu G, Surerus KK, Cowan JA (2002) Iron–sulfur cluster biosynthesis. Kinetic analysis of [2Fe-2S] cluster transfer from holo ISU to apo Fd: role of redox chemistry and a conserved aspartate. Biochemistry 41:8876–8885
Yaffe MP, Stuurman N, Vale RD (2003) Mitochondrial positioning in fission yeast is driven by association with dynamic microtubules and mitotic spindle poles. Proc Natl Acad Sci USA 100:11424–11428
Yarlett N, Hackstein JHP (2005) Hydrogenosomes: one organelle, multiple origins. Bioscience 55:657–667
Youssef NN, Hammond D (1971) The fine structure of the developmental stages of the microsporidian Nosema apis Zander. Tissue Cell 3:283–294
Yu Y, Samuelson J (1994) Primary structure of an Entamoeba histolytica nicotinamide nucleotide transhydrogenase. Mol Biochem Parasitol 68:323–328
Zheng L, Cash VL, Flint DH, Dean DR (1998) Assembly of iron–sulfur clusters. Identification of an iscSUA-hscBA-fdx gene cluster from Azotobacter vinelandii. J Biol Chem 273:13264–13272
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Tachezy, J., Šmíd, O. (2007). Mitosomes in Parasitic Protists. In: Tachezy, J. (eds) Hydrogenosomes and Mitosomes: Mitochondria of Anaerobic Eukaryotes. Microbiology Monographs, vol 9. Springer, Berlin, Heidelberg. https://doi.org/10.1007/7171_2007_113
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