{"title":"印度喜马拉雅地区蓝羊(Pseudois nayaur)有丝分裂全基因组及其与其他近缘种的比较系统发育关系","authors":"Deepesh Saini, Prabhaker Yadav, Vishnupriya Kolipakam, Sambandam Sathyakumar, Sandeep Kumar Gupta","doi":"10.1016/j.angen.2023.200155","DOIUrl":null,"url":null,"abstract":"<div><p>The ‘<em>Bharal</em>’ or ‘Himalayan Blue Sheep’ (<span><em>Pseudois nayaur</em></span><span><span><span>) is endemic to the Himalayan and Tibetan Regions. There are gaps in the available database for the blue sheep mitogenome sequencing from the Indian region. We sequenced and characterized the whole mitogenome of one blue sheep individual using the Illumina Nova-seq 6000 platform, which was 16,718 bp in length. It included 13 protein-coding genes (PCGs), 22 transfer RNA genes (tRNAs), two ribosomal RNA genes (rRNAs), and one non-coding control region (D loop). It was compared with other complete mitochondrial </span>DNA sequences<span> of blue sheep from the NCBI database. The whole mitogenome of blue sheep was found to be highly AT-biased (60%) and had a positive AT skew (0.121) and a negative GC skew (−0.341). In 13 PCGs of blue sheep, Leucine (15.58%) and </span></span>tryptophan<span><span> (2.72%) occurred most frequently. A typical secondary cloverleaf structure was observed for all tRNA genes except for tRNA-Ser, where a stable structure of dihydrouridine did not develop. The </span>phylogenetic analysis showed Indian blue sheep population formed a separate clade with a genetic distance of 3.7 to 4.1% from the Chinese blue sheep population, suggesting it to be of a different lineage and genetically qualifies the status of distinct subspecies. The results of this study will help in further phylogenetic analysis of Indian blue sheep populations in the Western and Eastern Himalayan regions and in understanding lineage identification and evolution for further research.</span></span></p></div>","PeriodicalId":7893,"journal":{"name":"Animal Gene","volume":"29 ","pages":"Article 200155"},"PeriodicalIF":0.0000,"publicationDate":"2023-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The complete mitogenome of blue sheep (Pseudois nayaur) from the Indian Himalayan Region and its comparative phylogenetic relationship with other related species\",\"authors\":\"Deepesh Saini, Prabhaker Yadav, Vishnupriya Kolipakam, Sambandam Sathyakumar, Sandeep Kumar Gupta\",\"doi\":\"10.1016/j.angen.2023.200155\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The ‘<em>Bharal</em>’ or ‘Himalayan Blue Sheep’ (<span><em>Pseudois nayaur</em></span><span><span><span>) is endemic to the Himalayan and Tibetan Regions. There are gaps in the available database for the blue sheep mitogenome sequencing from the Indian region. We sequenced and characterized the whole mitogenome of one blue sheep individual using the Illumina Nova-seq 6000 platform, which was 16,718 bp in length. It included 13 protein-coding genes (PCGs), 22 transfer RNA genes (tRNAs), two ribosomal RNA genes (rRNAs), and one non-coding control region (D loop). It was compared with other complete mitochondrial </span>DNA sequences<span> of blue sheep from the NCBI database. The whole mitogenome of blue sheep was found to be highly AT-biased (60%) and had a positive AT skew (0.121) and a negative GC skew (−0.341). In 13 PCGs of blue sheep, Leucine (15.58%) and </span></span>tryptophan<span><span> (2.72%) occurred most frequently. A typical secondary cloverleaf structure was observed for all tRNA genes except for tRNA-Ser, where a stable structure of dihydrouridine did not develop. The </span>phylogenetic analysis showed Indian blue sheep population formed a separate clade with a genetic distance of 3.7 to 4.1% from the Chinese blue sheep population, suggesting it to be of a different lineage and genetically qualifies the status of distinct subspecies. The results of this study will help in further phylogenetic analysis of Indian blue sheep populations in the Western and Eastern Himalayan regions and in understanding lineage identification and evolution for further research.</span></span></p></div>\",\"PeriodicalId\":7893,\"journal\":{\"name\":\"Animal Gene\",\"volume\":\"29 \",\"pages\":\"Article 200155\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Animal Gene\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2352406523000118\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Biochemistry, Genetics and Molecular Biology\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Animal Gene","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2352406523000118","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 0
摘要
“巴拉尔”或“喜马拉雅蓝羊”(Pseudois nayaur)是喜马拉雅和西藏地区的特有种。印度地区蓝羊有丝分裂基因组测序的可用数据库存在缺口。我们使用Illumina Nova seq 6000平台对一只蓝羊个体的整个有丝分裂基因组进行了测序和表征,该平台长度为16718bp。它包括13个蛋白质编码基因(PCG)、22个转移RNA基因(tRNA)、两个核糖体RNA基因(rRNA)和一个非编码控制区(D环)。将其与NCBI数据库中蓝羊的其他完整线粒体DNA序列进行了比较。蓝羊的整个有丝分裂基因组被发现具有高度的AT偏向性(60%),并且具有正的AT偏斜(0.121)和负的GC偏斜(-0.341)。在蓝羊的13个PCG中,亮氨酸(15.58%)和色氨酸(2.72%)最常见。除tRNA-Ser外,所有tRNA基因都观察到典型的二级苜蓿叶结构,其中没有形成稳定的二氢尿苷结构。系统发育分析表明,印度蓝羊种群与中国蓝羊种群形成了一个独立的分支,遗传距离为3.7-4.1%,表明它是一个不同的谱系,在遗传上符合不同亚种的地位。这项研究的结果将有助于对喜马拉雅西部和东部地区的印度蓝羊种群进行进一步的系统发育分析,并有助于了解谱系鉴定和进化,以进行进一步的研究。
The complete mitogenome of blue sheep (Pseudois nayaur) from the Indian Himalayan Region and its comparative phylogenetic relationship with other related species
The ‘Bharal’ or ‘Himalayan Blue Sheep’ (Pseudois nayaur) is endemic to the Himalayan and Tibetan Regions. There are gaps in the available database for the blue sheep mitogenome sequencing from the Indian region. We sequenced and characterized the whole mitogenome of one blue sheep individual using the Illumina Nova-seq 6000 platform, which was 16,718 bp in length. It included 13 protein-coding genes (PCGs), 22 transfer RNA genes (tRNAs), two ribosomal RNA genes (rRNAs), and one non-coding control region (D loop). It was compared with other complete mitochondrial DNA sequences of blue sheep from the NCBI database. The whole mitogenome of blue sheep was found to be highly AT-biased (60%) and had a positive AT skew (0.121) and a negative GC skew (−0.341). In 13 PCGs of blue sheep, Leucine (15.58%) and tryptophan (2.72%) occurred most frequently. A typical secondary cloverleaf structure was observed for all tRNA genes except for tRNA-Ser, where a stable structure of dihydrouridine did not develop. The phylogenetic analysis showed Indian blue sheep population formed a separate clade with a genetic distance of 3.7 to 4.1% from the Chinese blue sheep population, suggesting it to be of a different lineage and genetically qualifies the status of distinct subspecies. The results of this study will help in further phylogenetic analysis of Indian blue sheep populations in the Western and Eastern Himalayan regions and in understanding lineage identification and evolution for further research.
Animal GeneAgricultural and Biological Sciences-Insect Science
自引率
0.00%
发文量
16
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.