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Genome‐wide comparative identification and analysis of membrane‐FADS‐like superfamily genes in freshwater economic fishes
Membrane fatty acid desaturase (FADS)‐like superfamily proteins (FADSs) are essential for the synthesis of unsaturated fatty acids (UFAs). Recently, studies on FADS in fishes have mostly focused on marine species, and a comprehensive analysis of the FADS superfamily, including the FADS, stearoyl‐CoA...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10240347/ https://www.ncbi.nlm.nih.gov/pubmed/36883721 http://dx.doi.org/10.1002/2211-5463.13594 |
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author | Zhang, Yuru Zhang, Junmei Gao, Kedi Lu, Ronghua Cao, Xianglin Yang, Liping Nie, Guoxing |
author_facet | Zhang, Yuru Zhang, Junmei Gao, Kedi Lu, Ronghua Cao, Xianglin Yang, Liping Nie, Guoxing |
author_sort | Zhang, Yuru |
collection | PubMed |
description | Membrane fatty acid desaturase (FADS)‐like superfamily proteins (FADSs) are essential for the synthesis of unsaturated fatty acids (UFAs). Recently, studies on FADS in fishes have mostly focused on marine species, and a comprehensive analysis of the FADS superfamily, including the FADS, stearoyl‐CoA desaturase (SCD), and sphingolipid delta 4‐desaturase (DEGS) families, in freshwater economic fishes is urgently required. To this end, we conducted a thorough analysis of the number, gene/protein structure, chromosomal location, gene linkage map, phylogeny, and expression of the FADS superfamily. We identified 156 FADSs genes in the genome of 27 representative species. Notably, FADS1 and SCD5 were lost in most freshwater fish and other teleosts. All FADSs proteins contain 4 transmembrane helices and 2–3 amphipathic α‐helices. FADSs in the same family are often linked on the same chromosome; moreover, FADS and SCD or DEGS are frequently collocated on the same chromosome. In addition, FADS, SCD, and DEGS family proteins share similar evolutionary patterns. Interestingly, FADS6, as a member of the FADS family, exhibits a similar gene structure and chromosome location to that of SCD family members, which may be the transitional form of FADS and SCD. This study shed light on the type, structure, and phylogenetic relationship of FADSs in freshwater fishes, offering a new perspective into the functional mechanism analysis of FADSs. |
format | Online Article Text |
id | pubmed-10240347 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102403472023-06-06 Genome‐wide comparative identification and analysis of membrane‐FADS‐like superfamily genes in freshwater economic fishes Zhang, Yuru Zhang, Junmei Gao, Kedi Lu, Ronghua Cao, Xianglin Yang, Liping Nie, Guoxing FEBS Open Bio Research Articles Membrane fatty acid desaturase (FADS)‐like superfamily proteins (FADSs) are essential for the synthesis of unsaturated fatty acids (UFAs). Recently, studies on FADS in fishes have mostly focused on marine species, and a comprehensive analysis of the FADS superfamily, including the FADS, stearoyl‐CoA desaturase (SCD), and sphingolipid delta 4‐desaturase (DEGS) families, in freshwater economic fishes is urgently required. To this end, we conducted a thorough analysis of the number, gene/protein structure, chromosomal location, gene linkage map, phylogeny, and expression of the FADS superfamily. We identified 156 FADSs genes in the genome of 27 representative species. Notably, FADS1 and SCD5 were lost in most freshwater fish and other teleosts. All FADSs proteins contain 4 transmembrane helices and 2–3 amphipathic α‐helices. FADSs in the same family are often linked on the same chromosome; moreover, FADS and SCD or DEGS are frequently collocated on the same chromosome. In addition, FADS, SCD, and DEGS family proteins share similar evolutionary patterns. Interestingly, FADS6, as a member of the FADS family, exhibits a similar gene structure and chromosome location to that of SCD family members, which may be the transitional form of FADS and SCD. This study shed light on the type, structure, and phylogenetic relationship of FADSs in freshwater fishes, offering a new perspective into the functional mechanism analysis of FADSs. John Wiley and Sons Inc. 2023-03-16 /pmc/articles/PMC10240347/ /pubmed/36883721 http://dx.doi.org/10.1002/2211-5463.13594 Text en © 2023 The Authors. FEBS Open Bio published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Zhang, Yuru Zhang, Junmei Gao, Kedi Lu, Ronghua Cao, Xianglin Yang, Liping Nie, Guoxing Genome‐wide comparative identification and analysis of membrane‐FADS‐like superfamily genes in freshwater economic fishes |
title | Genome‐wide comparative identification and analysis of membrane‐FADS‐like superfamily genes in freshwater economic fishes |
title_full | Genome‐wide comparative identification and analysis of membrane‐FADS‐like superfamily genes in freshwater economic fishes |
title_fullStr | Genome‐wide comparative identification and analysis of membrane‐FADS‐like superfamily genes in freshwater economic fishes |
title_full_unstemmed | Genome‐wide comparative identification and analysis of membrane‐FADS‐like superfamily genes in freshwater economic fishes |
title_short | Genome‐wide comparative identification and analysis of membrane‐FADS‐like superfamily genes in freshwater economic fishes |
title_sort | genome‐wide comparative identification and analysis of membrane‐fads‐like superfamily genes in freshwater economic fishes |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10240347/ https://www.ncbi.nlm.nih.gov/pubmed/36883721 http://dx.doi.org/10.1002/2211-5463.13594 |
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