{"title":"线粒体基因组的分子进化是栗鼠半水栖适应性的基础","authors":"Qinguo Wei, Xibao Wang, Yuehuan Dong, Xuesong Mei, Yongquan Shang, Guolei Sun, Xiaoyang Wu, Xiaodong Gao, Chao Zhao, Weilai Sha, Honghai Zhang","doi":"10.1007/s13127-024-00650-1","DOIUrl":null,"url":null,"abstract":"<p>Lutrinae, which contains 13 otter species, is a semi-aquatic subfamily. They reclaimed semi-aquatic environments as their habitat. As aquatic environments can lead high energy loss, otters require a highly efficient energy generating style. Mitochondria play key roles in energy production and supply. Thus, we hypothesized that different selective constraints might influence the mitochondrial genomic DNA (mtDNA) of otters compared to that of other terrestrial Mustelidae. To verify the conjecture, we compared the evolutionary rate of the mitochondrial genomes of 12 otter species (including those we previously assembled from five otter species) with those of 18 terrestrial Mustelidae. The results showed that four of the 13 protein-coding genes (PCGs) (<i>COX2, ND1, ND4</i> and <i>ND6</i>) in the mitochondrial genomes of semi-aquatic otters possessed higher rate of non-synonymous nucleotide substitutions (<i>d</i><sub><i>N</i></sub>) to synonymous substitutions (<i>d</i><sub><i>S</i></sub>) (ω values, <i>d</i><sub><i>N</i></sub><i>/d</i><sub><i>S</i></sub>), than those in terrestrial Mustelidae. For two genes, <i>ND1</i> and <i>ND4</i>, this difference remained significant after controlling for evolutionary relationships using phylogenetic independent contrasts (PIC) analysis. Furthermore, <i>ND1</i> and <i>ND4</i> are rapidly evolving genes (REG)<i>.</i> Overall, these results demonstrate that <i>ND1</i> and <i>ND4</i> have undergone divergent evolutionary patterns between otters and terrestrial Mustelidae, along with their niche differentiation. The unique evolutionary pattern of mtDNA in Lutrinae may thus play an important role in their semi-aquatic habitat adaptation.</p>","PeriodicalId":54666,"journal":{"name":"Organisms Diversity & Evolution","volume":null,"pages":null},"PeriodicalIF":1.9000,"publicationDate":"2024-07-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Molecular evolution of the mitochondrial genome underlies semi-aquatic adaptation in lutrinae\",\"authors\":\"Qinguo Wei, Xibao Wang, Yuehuan Dong, Xuesong Mei, Yongquan Shang, Guolei Sun, Xiaoyang Wu, Xiaodong Gao, Chao Zhao, Weilai Sha, Honghai Zhang\",\"doi\":\"10.1007/s13127-024-00650-1\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Lutrinae, which contains 13 otter species, is a semi-aquatic subfamily. They reclaimed semi-aquatic environments as their habitat. As aquatic environments can lead high energy loss, otters require a highly efficient energy generating style. Mitochondria play key roles in energy production and supply. Thus, we hypothesized that different selective constraints might influence the mitochondrial genomic DNA (mtDNA) of otters compared to that of other terrestrial Mustelidae. To verify the conjecture, we compared the evolutionary rate of the mitochondrial genomes of 12 otter species (including those we previously assembled from five otter species) with those of 18 terrestrial Mustelidae. The results showed that four of the 13 protein-coding genes (PCGs) (<i>COX2, ND1, ND4</i> and <i>ND6</i>) in the mitochondrial genomes of semi-aquatic otters possessed higher rate of non-synonymous nucleotide substitutions (<i>d</i><sub><i>N</i></sub>) to synonymous substitutions (<i>d</i><sub><i>S</i></sub>) (ω values, <i>d</i><sub><i>N</i></sub><i>/d</i><sub><i>S</i></sub>), than those in terrestrial Mustelidae. For two genes, <i>ND1</i> and <i>ND4</i>, this difference remained significant after controlling for evolutionary relationships using phylogenetic independent contrasts (PIC) analysis. Furthermore, <i>ND1</i> and <i>ND4</i> are rapidly evolving genes (REG)<i>.</i> Overall, these results demonstrate that <i>ND1</i> and <i>ND4</i> have undergone divergent evolutionary patterns between otters and terrestrial Mustelidae, along with their niche differentiation. The unique evolutionary pattern of mtDNA in Lutrinae may thus play an important role in their semi-aquatic habitat adaptation.</p>\",\"PeriodicalId\":54666,\"journal\":{\"name\":\"Organisms Diversity & Evolution\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.9000,\"publicationDate\":\"2024-07-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organisms Diversity & Evolution\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1007/s13127-024-00650-1\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"EVOLUTIONARY BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organisms Diversity & Evolution","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s13127-024-00650-1","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"EVOLUTIONARY BIOLOGY","Score":null,"Total":0}
Molecular evolution of the mitochondrial genome underlies semi-aquatic adaptation in lutrinae
Lutrinae, which contains 13 otter species, is a semi-aquatic subfamily. They reclaimed semi-aquatic environments as their habitat. As aquatic environments can lead high energy loss, otters require a highly efficient energy generating style. Mitochondria play key roles in energy production and supply. Thus, we hypothesized that different selective constraints might influence the mitochondrial genomic DNA (mtDNA) of otters compared to that of other terrestrial Mustelidae. To verify the conjecture, we compared the evolutionary rate of the mitochondrial genomes of 12 otter species (including those we previously assembled from five otter species) with those of 18 terrestrial Mustelidae. The results showed that four of the 13 protein-coding genes (PCGs) (COX2, ND1, ND4 and ND6) in the mitochondrial genomes of semi-aquatic otters possessed higher rate of non-synonymous nucleotide substitutions (dN) to synonymous substitutions (dS) (ω values, dN/dS), than those in terrestrial Mustelidae. For two genes, ND1 and ND4, this difference remained significant after controlling for evolutionary relationships using phylogenetic independent contrasts (PIC) analysis. Furthermore, ND1 and ND4 are rapidly evolving genes (REG). Overall, these results demonstrate that ND1 and ND4 have undergone divergent evolutionary patterns between otters and terrestrial Mustelidae, along with their niche differentiation. The unique evolutionary pattern of mtDNA in Lutrinae may thus play an important role in their semi-aquatic habitat adaptation.
期刊介绍:
Organisms Diversity & Evolution (published by the Gesellschaft fuer Biologische Systematik, GfBS) is devoted to furthering our understanding of all aspects of organismal diversity and evolution. Papers addressing evolutionary aspects of the systematics, phylogenetics, morphology and development, taxonomy and biogeography of any group of eukaryotes, recent or fossil, are welcome. Priority is given to papers with a strong evolutionary and/or phylogenetic focus. Manuscripts presenting important methods or tools or addressing key theoretical, methodological, and philosophical principles related to the study of organismal diversity are also welcome. Species descriptions are welcome as parts of a manuscript of broader interest that strive to integrate such taxonomic information with the other areas of interest mentioned above.