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利用 SNP 基因分型芯片鉴定不同猪品种的全基因组拷贝数变异。

Identification of genome-wide copy number variations among diverse pig breeds using SNP genotyping arrays.

机构信息

Key Laboratory of Animal Genetics, Breeding and Reproduction, Ministry of Agriculture, National College of Animal Science and Technology, China Agricultural University, Beijing, China.

出版信息

PLoS One. 2013 Jul 23;8(7):e68683. doi: 10.1371/journal.pone.0068683. Print 2013.

DOI:10.1371/journal.pone.0068683
PMID:23935880
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3720780/
Abstract

Copy number variations (CNVs) are important forms of genetic variation complementary to SNPs, and can be considered as promising markers for some phenotypic and economically important traits or diseases susceptibility in domestic animals. In the present study, we performed a genome-wide CNV identification in 14 individuals selected from diverse populations, including six types of Chinese indigenous breeds, one Asian wild boar population, as well as three modern commercial foreign breeds. We identified 63 CNVRs in total, which covered 9.98 Mb of polymorphic sequence and corresponded to 0.36% of the genome sequence. The length of these CNVRs ranged from 3.20 to 827.21 kb, with an average of 158.37 kb and a median of 97.85 kb. Functional annotation revealed these identified CNVR have important molecular function, and may play an important role in exploring the genetic basis of phenotypic variability and disease susceptibility among pigs. Additionally, to confirm these potential CNVRs, we performed qPCR for 12 randomly selected CNVRs and 8 of them (66.67%) were confirmed successfully. CNVs detected in diverse populations herein are essential complementary to the CNV map in the pig genome, which provide an important resource for studies of genomic variation and the association between various economically important traits and CNVs.

摘要

拷贝数变异 (CNVs) 是遗传变异的重要形式,与 SNPs 互补,可以被认为是一些表型和经济上重要性状或疾病易感性的有前途的标记物。在本研究中,我们对来自不同群体的 14 个个体进行了全基因组 CNV 识别,包括 6 种中国本土品种、1 个亚洲野猪种群以及 3 个现代商业外国家畜品种。我们总共鉴定出 63 个 CNVR,覆盖了 9.98 Mb 的多态性序列,对应于基因组序列的 0.36%。这些 CNVR 的长度从 3.20 到 827.21 kb 不等,平均长度为 158.37 kb,中位数为 97.85 kb。功能注释表明,这些鉴定出的 CNVR 具有重要的分子功能,可能在探索猪的表型变异性和疾病易感性的遗传基础方面发挥重要作用。此外,为了确认这些潜在的 CNVR,我们对 12 个随机选择的 CNVR 进行了 qPCR,其中 8 个(66.67%)成功得到了确认。本文在不同群体中检测到的 CNVs 是猪基因组 CNV 图谱的重要补充,为基因组变异研究以及各种经济上重要性状与 CNVs 之间的关联提供了重要资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/754d/3720780/0ceef7e722c4/pone.0068683.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/754d/3720780/0ceef7e722c4/pone.0068683.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/754d/3720780/0ceef7e722c4/pone.0068683.g001.jpg

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