{"title":"The complete mitochondrial genome of Dama dama, and their phylogenetic relationships to other Cervidae","authors":"Rebecca Barnard, Judith Smith","doi":"10.1016/j.genrep.2024.102081","DOIUrl":null,"url":null,"abstract":"<div><div>This publication presents the complete mitochondrial genome of <em>Dama dama</em> along with in depth phylogenetic relationship and species divergence analysis in respect to other Cervidae. The mitochondrial genome presented here is 16,332 bp which is comprised of 13 genes, 2 rRNAs and 22 tRNAs. The mitochondrial genome for <em>Dama dama</em> is the smallest, compared to other Cervidae. Transfer RNA genes have a specific secondary structure, resembling a clover leaf, however, tRNA<sup>Ser</sup> (Serine 1) in <em>Dama dama</em> has been found to only have 3 arms, it is missing the dihydrouridine arm. The phylogenetic analysis conducted in this study compared the mitochondrial sequences from 25 different Cervidae species. Findings suggest that <em>Dama dama,</em> compared to other Cervidae, is most closely related to <em>Dama mesopotamica</em> and <em>Megaloceros giganteus.</em> With regards to <em>Dama dama</em>, the species divergence time from <em>Dama mesopotamica</em> and <em>Megaloceros giganteus</em> is 5.68 mya. Whereas the divergence time between <em>Dama mesopotamica</em> and <em>Megaloceros giganteus</em> is 5.35 mya. Our findings provide strong support for the distinction between <em>Dama dama</em> and <em>Dama mesopotamica</em> as a sub-species and a close evolutionary relationship between <em>Dama mesopotamica</em> and <em>Megaloceros giganteus</em>. Supporting previous reports of a sister-group relationship with a shared common ancestor. This study has provided a new perspective on the ancestral origin of the <em>Dama</em> genus, which can be further investigated using the <em>Dama dama</em> mitochondrial genome presented in this report. Understanding the evolution of <em>Dama dama</em> may help to better understand the lack of genetic diversity within the species and advance future management strategies to resolve this.</div></div>","PeriodicalId":12673,"journal":{"name":"Gene Reports","volume":"37 ","pages":"Article 102081"},"PeriodicalIF":1.0000,"publicationDate":"2024-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Gene Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2452014424002048","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0
Abstract
This publication presents the complete mitochondrial genome of Dama dama along with in depth phylogenetic relationship and species divergence analysis in respect to other Cervidae. The mitochondrial genome presented here is 16,332 bp which is comprised of 13 genes, 2 rRNAs and 22 tRNAs. The mitochondrial genome for Dama dama is the smallest, compared to other Cervidae. Transfer RNA genes have a specific secondary structure, resembling a clover leaf, however, tRNASer (Serine 1) in Dama dama has been found to only have 3 arms, it is missing the dihydrouridine arm. The phylogenetic analysis conducted in this study compared the mitochondrial sequences from 25 different Cervidae species. Findings suggest that Dama dama, compared to other Cervidae, is most closely related to Dama mesopotamica and Megaloceros giganteus. With regards to Dama dama, the species divergence time from Dama mesopotamica and Megaloceros giganteus is 5.68 mya. Whereas the divergence time between Dama mesopotamica and Megaloceros giganteus is 5.35 mya. Our findings provide strong support for the distinction between Dama dama and Dama mesopotamica as a sub-species and a close evolutionary relationship between Dama mesopotamica and Megaloceros giganteus. Supporting previous reports of a sister-group relationship with a shared common ancestor. This study has provided a new perspective on the ancestral origin of the Dama genus, which can be further investigated using the Dama dama mitochondrial genome presented in this report. Understanding the evolution of Dama dama may help to better understand the lack of genetic diversity within the species and advance future management strategies to resolve this.
Gene ReportsBiochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.30
自引率
7.70%
发文量
246
审稿时长
49 days
期刊介绍:
Gene Reports publishes papers that focus on the regulation, expression, function and evolution of genes in all biological contexts, including all prokaryotic and eukaryotic organisms, as well as viruses. Gene Reports strives to be a very diverse journal and topics in all fields will be considered for publication. Although not limited to the following, some general topics include: DNA Organization, Replication & Evolution -Focus on genomic DNA (chromosomal organization, comparative genomics, DNA replication, DNA repair, mobile DNA, mitochondrial DNA, chloroplast DNA). Expression & Function - Focus on functional RNAs (microRNAs, tRNAs, rRNAs, mRNA splicing, alternative polyadenylation) Regulation - Focus on processes that mediate gene-read out (epigenetics, chromatin, histone code, transcription, translation, protein degradation). Cell Signaling - Focus on mechanisms that control information flow into the nucleus to control gene expression (kinase and phosphatase pathways controlled by extra-cellular ligands, Wnt, Notch, TGFbeta/BMPs, FGFs, IGFs etc.) Profiling of gene expression and genetic variation - Focus on high throughput approaches (e.g., DeepSeq, ChIP-Seq, Affymetrix microarrays, proteomics) that define gene regulatory circuitry, molecular pathways and protein/protein networks. Genetics - Focus on development in model organisms (e.g., mouse, frog, fruit fly, worm), human genetic variation, population genetics, as well as agricultural and veterinary genetics. Molecular Pathology & Regenerative Medicine - Focus on the deregulation of molecular processes in human diseases and mechanisms supporting regeneration of tissues through pluripotent or multipotent stem cells.