Haoyuan Zhang, Pengcheng Ruan, He Cong, Lu Xu, Baigao Yang, Tao Ren, Dongjie Zhang, Hongyue Chen, Pengfei Hu, Zhen Wang, Hongmei Pan, Xiuqin Yang, Yanguo Han, Yan Zeng, Yongju Zhao, Di Liu, Simone Ceccobelli, Guangxin E
{"title":"猪驯化和适应的基因组学启示:利用全基因组选择分析和多个公共数据集的综合方法。","authors":"Haoyuan Zhang, Pengcheng Ruan, He Cong, Lu Xu, Baigao Yang, Tao Ren, Dongjie Zhang, Hongyue Chen, Pengfei Hu, Zhen Wang, Hongmei Pan, Xiuqin Yang, Yanguo Han, Yan Zeng, Yongju Zhao, Di Liu, Simone Ceccobelli, Guangxin E","doi":"10.3390/ani14213159","DOIUrl":null,"url":null,"abstract":"<p><p>As a global focus of animal husbandry, pigs provide essential meat resources for humans. Therefore, analyzing the genetic basis of adaptability, domestication, and artificial selection in pigs will contribute to further breeding. This study performed a genome-wide selection sweep analysis to identify candidate genes related to domestication and adaptive selection via data from 2413 public genotypes. Two complementary statistical analyses, <i>F<sub>ST</sub></i> (fixation index) and XP-EHH (cross-population extended haplotype homozygosity) were applied. The results revealed that numerous candidate genes were associated with high-altitude adaptability (e.g., <i>SIRPA</i>, <i>FRS2</i>, and <i>GRIN2B</i>) and habitat temperature adaptability (e.g., <i>MITF</i>, <i>PI3KC2A</i>, and <i>FRS2</i>). In addition, candidate genes related to the domestic genetic imprint of indigenous pigs (e.g., <i>TNR</i>, <i>NOCT</i>, and <i>SPATA5</i>) and strong artificial selection pressure in commercial breeds (e.g., <i>ITPR2</i>, <i>HSD17B12</i>, and <i>UGP2</i>) were identified in this study. Specifically, some MHC-related genes (e.g., <i>ZRTB12</i>, <i>TRIM26</i>, and <i>C7H6orf15</i>) were also under selection during domestication and artificial selection. Additionally, a phylogenetic comparative analysis revealed that the genetic divergence between populations does not fully follow the geographical distribution and management history in the major histocompatibility complex region/major histocompatibility complex II haplotypes, unlike that of the genome-wide genotypes. Furthermore, the higher heterozygosity and haplotype alleles of MHC reduce the differences between populations. Briefly, this study not only helps promote the relative theoretical understanding of environmental adaptive selection and domestication but also provides a theoretical reference for disease-resistant breeding in pigs.</p>","PeriodicalId":7955,"journal":{"name":"Animals","volume":"14 21","pages":""},"PeriodicalIF":2.7000,"publicationDate":"2024-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11545170/pdf/","citationCount":"0","resultStr":"{\"title\":\"Genomic Insights into Pig Domestication and Adaptation: An Integrated Approach Using Genome-Wide Selection Analysis and Multiple Public Datasets.\",\"authors\":\"Haoyuan Zhang, Pengcheng Ruan, He Cong, Lu Xu, Baigao Yang, Tao Ren, Dongjie Zhang, Hongyue Chen, Pengfei Hu, Zhen Wang, Hongmei Pan, Xiuqin Yang, Yanguo Han, Yan Zeng, Yongju Zhao, Di Liu, Simone Ceccobelli, Guangxin E\",\"doi\":\"10.3390/ani14213159\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>As a global focus of animal husbandry, pigs provide essential meat resources for humans. Therefore, analyzing the genetic basis of adaptability, domestication, and artificial selection in pigs will contribute to further breeding. This study performed a genome-wide selection sweep analysis to identify candidate genes related to domestication and adaptive selection via data from 2413 public genotypes. Two complementary statistical analyses, <i>F<sub>ST</sub></i> (fixation index) and XP-EHH (cross-population extended haplotype homozygosity) were applied. The results revealed that numerous candidate genes were associated with high-altitude adaptability (e.g., <i>SIRPA</i>, <i>FRS2</i>, and <i>GRIN2B</i>) and habitat temperature adaptability (e.g., <i>MITF</i>, <i>PI3KC2A</i>, and <i>FRS2</i>). In addition, candidate genes related to the domestic genetic imprint of indigenous pigs (e.g., <i>TNR</i>, <i>NOCT</i>, and <i>SPATA5</i>) and strong artificial selection pressure in commercial breeds (e.g., <i>ITPR2</i>, <i>HSD17B12</i>, and <i>UGP2</i>) were identified in this study. Specifically, some MHC-related genes (e.g., <i>ZRTB12</i>, <i>TRIM26</i>, and <i>C7H6orf15</i>) were also under selection during domestication and artificial selection. Additionally, a phylogenetic comparative analysis revealed that the genetic divergence between populations does not fully follow the geographical distribution and management history in the major histocompatibility complex region/major histocompatibility complex II haplotypes, unlike that of the genome-wide genotypes. Furthermore, the higher heterozygosity and haplotype alleles of MHC reduce the differences between populations. 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Genomic Insights into Pig Domestication and Adaptation: An Integrated Approach Using Genome-Wide Selection Analysis and Multiple Public Datasets.
As a global focus of animal husbandry, pigs provide essential meat resources for humans. Therefore, analyzing the genetic basis of adaptability, domestication, and artificial selection in pigs will contribute to further breeding. This study performed a genome-wide selection sweep analysis to identify candidate genes related to domestication and adaptive selection via data from 2413 public genotypes. Two complementary statistical analyses, FST (fixation index) and XP-EHH (cross-population extended haplotype homozygosity) were applied. The results revealed that numerous candidate genes were associated with high-altitude adaptability (e.g., SIRPA, FRS2, and GRIN2B) and habitat temperature adaptability (e.g., MITF, PI3KC2A, and FRS2). In addition, candidate genes related to the domestic genetic imprint of indigenous pigs (e.g., TNR, NOCT, and SPATA5) and strong artificial selection pressure in commercial breeds (e.g., ITPR2, HSD17B12, and UGP2) were identified in this study. Specifically, some MHC-related genes (e.g., ZRTB12, TRIM26, and C7H6orf15) were also under selection during domestication and artificial selection. Additionally, a phylogenetic comparative analysis revealed that the genetic divergence between populations does not fully follow the geographical distribution and management history in the major histocompatibility complex region/major histocompatibility complex II haplotypes, unlike that of the genome-wide genotypes. Furthermore, the higher heterozygosity and haplotype alleles of MHC reduce the differences between populations. Briefly, this study not only helps promote the relative theoretical understanding of environmental adaptive selection and domestication but also provides a theoretical reference for disease-resistant breeding in pigs.
AnimalsAgricultural and Biological Sciences-Animal Science and Zoology
CiteScore
4.90
自引率
16.70%
发文量
3015
审稿时长
20.52 days
期刊介绍:
Animals (ISSN 2076-2615) is an international and interdisciplinary scholarly open access journal. It publishes original research articles, reviews, communications, and short notes that are relevant to any field of study that involves animals, including zoology, ethnozoology, animal science, animal ethics and animal welfare. However, preference will be given to those articles that provide an understanding of animals within a larger context (i.e., the animals'' interactions with the outside world, including humans). There is no restriction on the length of the papers. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible. Full experimental details and/or method of study, must be provided for research articles. Articles submitted that involve subjecting animals to unnecessary pain or suffering will not be accepted, and all articles must be submitted with the necessary ethical approval (please refer to the Ethical Guidelines for more information).