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Discovery of the Elusive Leptin in Birds: Identification of Several ‘Missing Links’ in the Evolution of Leptin and Its Receptor

Leptin is a pleiotropic protein best known for regulation of appetite and fat storage in mammals. While many leptin orthologs have been identified among vertebrates, an authentic leptin in birds has remained elusive and controversial. Here we identify leptin sequence from the Peregrine falcon, Falco...

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Autores principales: Prokop, Jeremy W., Schmidt, Cameron, Gasper, Donald, Duff, Robert J., Milsted, Amy, Ohkubo, Takeshi, Ball, Hope C., Shawkey, Matthew D., Mays, Herman L., Cogburn, Larry A., Londraville, Richard L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3963946/
https://www.ncbi.nlm.nih.gov/pubmed/24663438
http://dx.doi.org/10.1371/journal.pone.0092751
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author Prokop, Jeremy W.
Schmidt, Cameron
Gasper, Donald
Duff, Robert J.
Milsted, Amy
Ohkubo, Takeshi
Ball, Hope C.
Shawkey, Matthew D.
Mays, Herman L.
Cogburn, Larry A.
Londraville, Richard L.
author_facet Prokop, Jeremy W.
Schmidt, Cameron
Gasper, Donald
Duff, Robert J.
Milsted, Amy
Ohkubo, Takeshi
Ball, Hope C.
Shawkey, Matthew D.
Mays, Herman L.
Cogburn, Larry A.
Londraville, Richard L.
author_sort Prokop, Jeremy W.
collection PubMed
description Leptin is a pleiotropic protein best known for regulation of appetite and fat storage in mammals. While many leptin orthologs have been identified among vertebrates, an authentic leptin in birds has remained elusive and controversial. Here we identify leptin sequence from the Peregrine falcon, Falco peregrinus (pfleptin), and identify sequences from two other birds (mallard and zebra finch), and ‘missing’ vertebrates (elephant shark, alligator, Indian python, Chinese soft-shelled turtle, and coelacanth). The pattern of genes surrounding leptin (snd1, rbm28) is syntenic between the falcon and mammalian genomes. Phylogenetic analysis of all known leptin protein sequences improves our understanding of leptin’s evolution. Structural modeling of leptin orthologs highlights a highly conserved hydrophobic core in the four-helix cytokine packing domain. A docked model of leptin with the leptin receptor for Peregrine falcon reveals several conserved amino acids important for the interaction and possible coevolution of leptin with its receptor. We also show for the first time, an authentic avian leptin sequence that activates the JAK-STAT signaling pathway. These newly identified sequences, structures, and tools for avian leptin and its receptor will allow elucidation of the function of these proteins in feral and domestic birds.
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spelling pubmed-39639462014-03-27 Discovery of the Elusive Leptin in Birds: Identification of Several ‘Missing Links’ in the Evolution of Leptin and Its Receptor Prokop, Jeremy W. Schmidt, Cameron Gasper, Donald Duff, Robert J. Milsted, Amy Ohkubo, Takeshi Ball, Hope C. Shawkey, Matthew D. Mays, Herman L. Cogburn, Larry A. Londraville, Richard L. PLoS One Research Article Leptin is a pleiotropic protein best known for regulation of appetite and fat storage in mammals. While many leptin orthologs have been identified among vertebrates, an authentic leptin in birds has remained elusive and controversial. Here we identify leptin sequence from the Peregrine falcon, Falco peregrinus (pfleptin), and identify sequences from two other birds (mallard and zebra finch), and ‘missing’ vertebrates (elephant shark, alligator, Indian python, Chinese soft-shelled turtle, and coelacanth). The pattern of genes surrounding leptin (snd1, rbm28) is syntenic between the falcon and mammalian genomes. Phylogenetic analysis of all known leptin protein sequences improves our understanding of leptin’s evolution. Structural modeling of leptin orthologs highlights a highly conserved hydrophobic core in the four-helix cytokine packing domain. A docked model of leptin with the leptin receptor for Peregrine falcon reveals several conserved amino acids important for the interaction and possible coevolution of leptin with its receptor. We also show for the first time, an authentic avian leptin sequence that activates the JAK-STAT signaling pathway. These newly identified sequences, structures, and tools for avian leptin and its receptor will allow elucidation of the function of these proteins in feral and domestic birds. Public Library of Science 2014-03-24 /pmc/articles/PMC3963946/ /pubmed/24663438 http://dx.doi.org/10.1371/journal.pone.0092751 Text en © 2014 Prokop et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Prokop, Jeremy W.
Schmidt, Cameron
Gasper, Donald
Duff, Robert J.
Milsted, Amy
Ohkubo, Takeshi
Ball, Hope C.
Shawkey, Matthew D.
Mays, Herman L.
Cogburn, Larry A.
Londraville, Richard L.
Discovery of the Elusive Leptin in Birds: Identification of Several ‘Missing Links’ in the Evolution of Leptin and Its Receptor
title Discovery of the Elusive Leptin in Birds: Identification of Several ‘Missing Links’ in the Evolution of Leptin and Its Receptor
title_full Discovery of the Elusive Leptin in Birds: Identification of Several ‘Missing Links’ in the Evolution of Leptin and Its Receptor
title_fullStr Discovery of the Elusive Leptin in Birds: Identification of Several ‘Missing Links’ in the Evolution of Leptin and Its Receptor
title_full_unstemmed Discovery of the Elusive Leptin in Birds: Identification of Several ‘Missing Links’ in the Evolution of Leptin and Its Receptor
title_short Discovery of the Elusive Leptin in Birds: Identification of Several ‘Missing Links’ in the Evolution of Leptin and Its Receptor
title_sort discovery of the elusive leptin in birds: identification of several ‘missing links’ in the evolution of leptin and its receptor
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3963946/
https://www.ncbi.nlm.nih.gov/pubmed/24663438
http://dx.doi.org/10.1371/journal.pone.0092751
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