Iron testes: sperm mitochondria as a context for dissecting iron metabolism
© Hales; licensee BioMed Central Ltd. 2010
Received: 25 May 2010
Accepted: 10 June 2010
Published: 21 June 2010
A recent paper in BMC Developmental Biology reports that a mitochondrial iron importer is required for Drosophila male fertility and normal mitochondrial shaping in spermatids. This suggests that mitochondrial morphogenesis during insect spermatogenesis may be a useful new context in which to study iron metabolism.
See research article http://0-www.biomedcentral.com.brum.beds.ac.uk/1471-213X/10/68
In a recent study published in BMC Developmental Biology, Metzendorf and Lind  establish Drosophila spermatogenesis as an emerging context for the study of mitochondrial iron metabolism through their analysis of the Drosophila gene mitoferrin (dmfrn). During spermatid development in flies, mitochondria undergo dramatic events of movement and shaping, including aggregation, fusion and elongation beside the growing flagellar axoneme. Disruptions of mitochondrial function or dynamics typically affect male fertility, a phenotype that is easily screened for and characterized at the subcellular level. The dmfrn gene product and other iron metabolism proteins show enriched expression in the testes of mammals and insects, suggesting special roles for mitochondrial iron metabolism in spermatogenesis. Analysis of these requirements in insect spermatogenesis could lead to new insights into human genetic disorders such as Friedreich's ataxia and sideroblastic anemia, both associated with defects in iron homeostasis within mitochondrial compartments.
Metzendorf and Lind characterized D. melanogaster mitoferrin (dmfrn) mutants and showed that the Dmfrn mitochondrial iron importer is required for spermatid mitochondrial morphogenesis and thus for development of mature motile sperm . As in other invertebrates, the Drosophila genome includes a single homolog, dmfrn, of two human paralogs, mitoferrin-1 and mitoferrin-2, and two Saccharomyces cerevisiae paralogs, mrs3 and mrs4; all tests of cross-species complementation so far have indicated strong functional conservation. Studies in vertebrates and yeast demonstrate a role for mitoferrin family members in import of iron from the cytosol into mitochondria [3, 4]. Metzendorf and Lind characterized three hypomorphic transposable element insertion alleles and two deficiency alleles affecting dmfrn. All alleles were associated with male sterility, and the deficiency alleles were associated with only a mild decrease in viability. The testis phenotype was enhanced and suppressed, respectively, by low and high iron levels in food.
At the ultrastructural level, as detected by transmission electron microscopy (TEM), dmfrn spermatid axonemes were associated with abnormally configured mitochondrial derivatives. Wild-type spermatid axonemes in TEM cross-section are accompanied by a major mitochondrial derivative containing electron-dense paracrystalline material; the minor mitochondrial derivative lacks this material and is mostly stripped away in the waste bag during individualization. Mutant dmfrn spermatids showed a striking decrease in paracrystalline material and aberrant distribution of what little was present, consistent with the speculation that iron may be a component of this yet-uncharacterized material (Figure 2). This paracrystalline material is proposed to provide a certain level of structural rigidity important for proper sperm movement before and during fertilization. The lack of paracrystalline material in dmfrn sperm cross-sections might alternatively simply reflect mitochondrial elongation failure.
Additional TEM data, combined with staining of actin and other structures, indicated that sperm individualization typically failed in dmfrn mutants. Individualization is the process at the end of spermatogenesis during which the 64 interconnected spermatids in a cyst become surrounded by their own plasma membranes. Failure of individualization is a typical secondary phenotype in mutant testes with an earlier structural defect.
The lack of dramatic phenotypes in tissues other than the testis led the authors to confirm by RT-PCR that mitoferrin showed enriched expression in testis tissue. A dmfrn-lacZ reporter construct indicated protein expression in post-meiotic spermatids. A tagged and functional dmfrn was associated with mitochondria in early round spermatids and later stages, with much of the protein sent to the waste bag during individualization. At the RNA level, the authors found similar testis enrichment of two additional iron-metabolism genes, fh and Fer3HCH. Expression patterns of these genes plus another, Abcb10, together suggest that Drosophila spermatogenesis could be a fruitful context for further analysis of iron metabolism.
The Drosophila fh gene is the ortholog of S. cerevisiae YFH1 and of human FXN, a gene associated with the neurodegenerative disorder Friedreich's ataxia. FXN encodes frataxin, a mitochondrial matrix protein whose role appears to be the delivery of iron to the scaffolding proteins on which Fe-S clusters are formed . These Fe-S clusters later act as cofactors in many proteins important for cellular respiration. Frataxin may also play a role in the simple binding and detoxification of iron. Neurodegeneration in humans with Friedrich's ataxia stems from increased mitochondrial iron levels and neural oxidative damage; decreased levels of Fe-S-containing proteins presumably activate a pathway to boost mitoferrin-based iron import into mitochondria. Drosophila frataxin is expressed in multiple tissues besides the testis and, unlike mitoferrin, appears essential for normal viability. Studies of Drosophila frataxin are now possible through RNA interference ; perhaps future work will enable analysis in the testis.
In mammals, the ABC-family transporter protein Abcb10 forms a complex with mitoferrin-1 and increases iron import into mitochondria, as recently characterized in erythroid tissue . A close homolog in Drosophila is evident through sequence homology searches of the Drosophila genome ; the FlyAtlas database reports that this gene shows enriched expression in both testes and ovaries in Drosophila . Analysis of the fly version of Abcb10 may enable exploration of genetic interactions with dmfrn and the physical interactions of their gene products. Ferritin is an iron-sequestration protein that has been extensively studied in its cytosolic and secreted forms. Recent years have seen the discovery of a new ferritin in mammals and insects that is targeted to mitochondria. Drosophila mitochondrial ferritin, encoded by Fer3HCH, is highly expressed in the testis, and the gene product localizes to mitochondria when transfected into human cells . This gene is ripe for analysis with regard to its role in spermatogenesis and its interactions with mitoferrin, fh, and Abcb10. Mammalian mitochondrial ferritin is similarly expressed highly in testes ; broader studies of human male fertility may in the future lead to a focus on iron metabolism in developing sperm.
Metzendorf and Lind's identification of a role for the mitochondrial iron importer dmfrn in Drosophila sperm development, and their confirmation of testis expression of other proteins involved in iron homeostasis, set the stage for future exploration of iron metabolism as an important factor in mitochondrial morphogenesis and fertility in both vertebrates and invertebrates.
Work in the author's lab is supported by National Institutes of Health Academic Research Enhancement Grant R15GM080689. The FlyBase and FlyAtlas databases provided important information.
- Andrews NC: Forging a field: the golden age of iron biology. Blood. 2008, 112: 219-230. 10.1182/blood-2007-12-077388.PubMed CentralView ArticlePubMedGoogle Scholar
- Metzendorf C, Lind MI: Drosophila mitoferrin is essential for male fertility: evidence for a role of mitochondrial iron metabolism during spermatogenesis. BMC Dev Biol. 2010, 10: 68-PubMed CentralView ArticlePubMedGoogle Scholar
- Paradkar PN, Zumbrennen KB, Paw BH, Ward DM, Kaplan J: Regulation of mitochondrial iron import through differential turnover of mitoferrin 1 and mitoferrin 2. Mol Cell Biol. 2009, 29: 1007-1016. 10.1128/MCB.01685-08.PubMed CentralView ArticlePubMedGoogle Scholar
- Zhang Y, Lyver ER, Knight SA, Pain D, Lesuisse E, Dancis A: Mrs3p, Mrs4p, and frataxin provide iron for Fe-S cluster synthesis in mitochondria. J Biol Chem. 2006, 281: 22493-22502. 10.1074/jbc.M604246200.View ArticlePubMedGoogle Scholar
- Anderson PR, Kirby K, Orr WC, Hilliker AJ, Phillips JP: Hydrogen peroxide scavenging rescues frataxin deficiency in a Drosophila model of Friedreich's ataxia. Proc Natl Acad Sci USA. 2008, 105: 611-616. 10.1073/pnas.0709691105.PubMed CentralView ArticlePubMedGoogle Scholar
- Chen W, Paradkar PN, Li L, Pierce EL, Langer NB, Takahashi-Makise N, Hyde BB, Shirihai OS, Ward DM, Kaplan J, Paw BH: Abcb10 physically interacts with mitoferrin-1 (Slc25a37) to enhance its stability and function in the erythroid mitochondria. Proc Natl Acad Sci USA. 2009, 106: 16263-16268. 10.1073/pnas.0904519106.PubMed CentralView ArticlePubMedGoogle Scholar
- Tweedie S, Ashburner M, Falls K, Leyland P, McQuilton P, Marygold S, Millburn G, Osumi-Sutherland D, Schroeder A, Seal R, Zhang H: FlyBase Consortium: FlyBase: enhancing Drosophila Gene Ontology annotations. Nucleic Acids Res. 2009, 37: D555-D559. 10.1093/nar/gkn788.PubMed CentralView ArticlePubMedGoogle Scholar
- Chintapalli VR, Wang J, Dow JA: Using FlyAtlas to identify better Drosophila melanogaster models of human disease. Nat Genet. 2007, 39: 715-720. 10.1038/ng2049.View ArticlePubMedGoogle Scholar
- Missirlis F, Holmberg S, Georgieva T, Dunkov BC, Rouault TA, Law JH: Characterization of mitochondrial ferritin in Drosophila. Proc Natl Acad Sci USA. 2006, 103: 5893-5898. 10.1073/pnas.0601471103.PubMed CentralView ArticlePubMedGoogle Scholar
- Santambrogio P, Biasiotto G, Sanvito F, Olivieri S, Arosio P, Levi S: Mitochondrial ferritin expression in adult mouse tissues. J Histochem Cytochem. 2007, 55: 1129-1137. 10.1369/jhc.7A7273.2007.PubMed CentralView ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.