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Abstract Iron is essential to life, but surprisingly little is known about how iron is managed in nonvertebrate animals. In mammals, the well‐characterizedtransferrinsbind iron and are involved in iron transport or immunity, whereas other members of thetransferrinfamily do not have a role in iron homeostasis. In insects, the functions oftransferrinsare still poorly understood. The goals of this project were to identify thetransferringenes in a diverse set of insect species, resolve the evolutionary relationships among these genes, and predict which of thetransferrinsare likely to have a role in iron homeostasis. Our phylogenetic analysis oftransferrinsfrom 16 orders of insects and two orders of noninsect hexapods demonstrated that there are four orthologous groups of insecttransferrins. Our analysis suggests thattransferrin 2arose prior to the origin of insects, andtransferrins 1,3, and4arose early in insect evolution. Primary sequence analysis of each of the insecttransferrinswas used to predict signal peptides, carboxyl‐terminal transmembrane regions, GPI‐anchors, and iron binding. Based on this analysis, we suggest thattransferrins 2,3, and4are unlikely to play a major role in iron homeostasis. In contrast, thetransferrin 1orthologs are predicted to be secreted, soluble, iron‐binding proteins. We conclude thattransferrin 1orthologs are the most likely to play an important role in iron homeostasis. Interestingly, it appears that the louse, aphid, and thrips lineages have lost thetransferrin 1gene and, thus, have evolved to manage iron withouttransferrins.
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Structural insight into the novel iron‐coordination and domain interactions of transferrin‐1 from a model insect, Manduca sexta
Abstract Transferrins function in iron sequestration and iron transport by binding iron tightly and reversibly. Vertebrate transferrins coordinate iron through interactions with two tyrosines, an aspartate, a histidine, and a carbonate anion, and conformational changes that occur upon iron binding and release have been described. Much less is known about the structure and functions of insect transferrin‐1 (Tsf1), which is present in hemolymph and influences iron homeostasis mostly by unknown mechanisms. Amino acid sequence and biochemical analyses have suggested that iron coordination by Tsf1 differs from that of the vertebrate transferrins. Here we report the first crystal structure (2.05 Å resolution) of an insect transferrin.Manduca sexta(MsTsf1) in the holo form exhibits a bilobal fold similar to that of vertebrate transferrins, but its carboxyl‐lobe adopts a novel orientation and contacts with the amino‐lobe. The structure revealed coordination of a single Fe3+ion in the amino‐lobe through Tyr90, Tyr204, and two carbonate anions. One carbonate anion is buried near the ferric ion and is coordinated by four residues, whereas the other carbonate anion is solvent exposed and coordinated by Asn121. Notably, these residues are highly conserved in Tsf1 orthologs. Docking analysis suggested that the solvent exposed carbonate position is capable of binding alternative anions. These findings provide a structural basis for understanding Tsf1 function in iron sequestration and transport in insects as well as insight into the similarities and differences in iron homeostasis between insects and humans.
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- Award ID(s):
- 1656388
- PAR ID:
- 10454630
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Protein Science
- Volume:
- 30
- Issue:
- 2
- ISSN:
- 0961-8368
- Page Range / eLocation ID:
- p. 408-422
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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