Evolution of the Vertebrate Resistin Gene Family
Resistin (encoded by Retn) was previously identified in rodents as a hormone associated with diabetes; however human resistin is instead linked to inflammation. Resistin is a member of a small gene family that includes the resistin-like peptides (encoded by Retnl genes) in mammals. Genomic searches...
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Published in | PloS one Vol. 10; no. 6; p. e0130188 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
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15.06.2015
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Abstract | Resistin (encoded by Retn) was previously identified in rodents as a hormone associated with diabetes; however human resistin is instead linked to inflammation. Resistin is a member of a small gene family that includes the resistin-like peptides (encoded by Retnl genes) in mammals. Genomic searches of available genome sequences of diverse vertebrates and phylogenetic analyses were conducted to determine the size and origin of the resistin-like gene family. Genes encoding peptides similar to resistin were found in Mammalia, Sauria, Amphibia, and Actinistia (coelacanth, a lobe-finned fish), but not in Aves or fish from Actinopterygii, Chondrichthyes, or Agnatha. Retnl originated by duplication and transposition from Retn on the early mammalian lineage after divergence of the platypus, but before the placental and marsupial mammal divergence. The resistin-like gene family illustrates an instance where the locus of origin of duplicated genes can be identified, with Retn continuing to reside at this location. Mammalian species typically have a single copy Retn gene, but are much more variable in their numbers of Retnl genes, ranging from 0 to 9. Since Retn is located at the locus of origin, thus likely retained the ancestral expression pattern, largely maintained its copy number, and did not display accelerated evolution, we suggest that it is more likely to have maintained an ancestral function, while Retnl, which transposed to a new location, displays accelerated evolution, and shows greater variability in gene number, including gene loss, likely evolved new, but potentially lineage-specific, functions. |
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AbstractList | Resistin (encoded by Retn) was previously identified in rodents as a hormone associated with diabetes; however human resistin is instead linked to inflammation. Resistin is a member of a small gene family that includes the resistin-like peptides (encoded by Retnl genes) in mammals. Genomic searches of available genome sequences of diverse vertebrates and phylogenetic analyses were conducted to determine the size and origin of the resistin-like gene family. Genes encoding peptides similar to resistin were found in Mammalia, Sauria, Amphibia, and Actinistia (coelacanth, a lobe-finned fish), but not in Aves or fish from Actinopterygii, Chondrichthyes, or Agnatha. Retnl originated by duplication and transposition from Retn on the early mammalian lineage after divergence of the platypus, but before the placental and marsupial mammal divergence. The resistin-like gene family illustrates an instance where the locus of origin of duplicated genes can be identified, with Retn continuing to reside at this location. Mammalian species typically have a single copy Retn gene, but are much more variable in their numbers of Retnl genes, ranging from 0 to 9. Since Retn is located at the locus of origin, thus likely retained the ancestral expression pattern, largely maintained its copy number, and did not display accelerated evolution, we suggest that it is more likely to have maintained an ancestral function, while Retnl, which transposed to a new location, displays accelerated evolution, and shows greater variability in gene number, including gene loss, likely evolved new, but potentially lineage-specific, functions. Resistin (encoded by Retn ) was previously identified in rodents as a hormone associated with diabetes; however human resistin is instead linked to inflammation. Resistin is a member of a small gene family that includes the resistin-like peptides (encoded by Retnl genes) in mammals. Genomic searches of available genome sequences of diverse vertebrates and phylogenetic analyses were conducted to determine the size and origin of the resistin-like gene family. Genes encoding peptides similar to resistin were found in Mammalia, Sauria, Amphibia, and Actinistia (coelacanth, a lobe-finned fish), but not in Aves or fish from Actinopterygii, Chondrichthyes, or Agnatha. Retnl originated by duplication and transposition from Retn on the early mammalian lineage after divergence of the platypus, but before the placental and marsupial mammal divergence. The resistin-like gene family illustrates an instance where the locus of origin of duplicated genes can be identified, with Retn continuing to reside at this location. Mammalian species typically have a single copy Retn gene, but are much more variable in their numbers of Retnl genes, ranging from 0 to 9. Since Retn is located at the locus of origin, thus likely retained the ancestral expression pattern, largely maintained its copy number, and did not display accelerated evolution, we suggest that it is more likely to have maintained an ancestral function, while Retnl , which transposed to a new location, displays accelerated evolution, and shows greater variability in gene number, including gene loss, likely evolved new, but potentially lineage-specific, functions. |
Audience | Academic |
Author | Hu, Qingda Irwin, David M Tan, Huanran |
AuthorAffiliation | 3 Banting and Best Diabetes Centre, University of Toronto, Toronto, Ontario, Canada 2 Department of Pharmacology, Health Sciences Center, Peking University, Beijing, China 1 Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada University of Lausanne, SWITZERLAND |
AuthorAffiliation_xml | – name: University of Lausanne, SWITZERLAND – name: 1 Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada – name: 3 Banting and Best Diabetes Centre, University of Toronto, Toronto, Ontario, Canada – name: 2 Department of Pharmacology, Health Sciences Center, Peking University, Beijing, China |
Author_xml | – sequence: 1 givenname: Qingda surname: Hu fullname: Hu, Qingda organization: Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada – sequence: 2 givenname: Huanran surname: Tan fullname: Tan, Huanran organization: Department of Pharmacology, Health Sciences Center, Peking University, Beijing, China – sequence: 3 givenname: David M surname: Irwin fullname: Irwin, David M organization: Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada; Department of Pharmacology, Health Sciences Center, Peking University, Beijing, China; Banting and Best Diabetes Centre, University of Toronto, Toronto, Ontario, Canada |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/26076481$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1371_journal_pone_0191904 crossref_primary_10_3389_fendo_2023_1155202 crossref_primary_10_3390_biom8020017 crossref_primary_10_3389_fimmu_2023_1172467 crossref_primary_10_1038_s41467_024_46070_9 crossref_primary_10_3389_fendo_2021_700066 crossref_primary_10_1007_s00251_020_01186_2 crossref_primary_10_3390_ijms241511918 |
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Copyright | COPYRIGHT 2015 Public Library of Science 2015 Hu et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. 2015 Hu et al 2015 Hu et al |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Conceived and designed the experiments: QH HT DMI. Performed the experiments: QH DMI. Analyzed the data: QH DMI. Contributed reagents/materials/analysis tools: QH HT DMI. Wrote the paper: QH HT DMI. Competing Interests: The authors have declared that no competing interests exist. |
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Snippet | Resistin (encoded by Retn) was previously identified in rodents as a hormone associated with diabetes; however human resistin is instead linked to... Resistin (encoded by Retn ) was previously identified in rodents as a hormone associated with diabetes; however human resistin is instead linked to... |
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SubjectTerms | Amino Acid Sequence Amphibia Amphibians Animals Biological Evolution Birds Chelonia mydas Copy number Diabetes mellitus Divergence Evolution Evolutionary biology Fish Gene duplication Gene sequencing Genes Genomes Genomics Humans Loci Mammals Mammals - genetics Molecular Sequence Data Multigene Family Peptides Phylogeny Placenta Platypus Reproduction (copying) Resistin - genetics Rodents Sequence Homology, Amino Acid Transposition Vertebrates |
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Title | Evolution of the Vertebrate Resistin Gene Family |
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