畜牧兽医学报 ›› 2023, Vol. 54 ›› Issue (8): 3252-3261.doi: 10.11843/j.issn.0366-6964.2023.08.012

• 遗传育种 • 上一篇    下一篇

一种快速挖掘鸡品种特征性SNP标记集合的方法

白露, 王梦杰, 马小春, 何政肖, 谭晓冬, 刘杰, 赵桂苹, 文杰, 刘冉冉*   

  1. 中国农业科学院北京畜牧兽医研究所 畜禽营养与饲养全国重点实验室 农业农村部动物遗传育种与繁殖(家禽)重点实验室, 北京 100193
  • 收稿日期:2023-02-17 出版日期:2023-08-23 发布日期:2023-08-22
  • 通讯作者: 刘冉冉,主要从事家禽遗传育种研究,E-mail:liuranran@caas.cn
  • 作者简介:白露(1999-),女,宁夏石嘴山人,硕士生,主要从事鸡遗传育种研究,E-mail:blu1130@163.com
  • 基金资助:
    国家重点研发计划项目(2022YFD1301600);国家肉鸡产业技术体系(CARS-41);核心种源攻关项目(JBGS〔2021〕107)

A Method for Quickly Mining the Characteristic SNP Markers Set of Chicken

BAI Lu, WANG Mengjie, MA Xiaochun, HE Zhengxiao, TAN Xiaodong, LIU Jie, ZHAO Guiping, WEN Jie, LIU Ranran*   

  1. Key Laboratory of Animal (Poultry) Genetics, Breeding and Reproduction of Ministry of Agriculture and Rural Affairs, National Key Laboratory of Livestock and Poultry Nutrition and Feeding, Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, China
  • Received:2023-02-17 Online:2023-08-23 Published:2023-08-22

摘要: 旨在建立一种快速挖掘鸡品种/品系特征性SNP标记集合的方法,实现通过少量SNP标记将目标品种/品系与其他品种/品系区分的目标。本研究以北京油鸡、京星黄鸡、7个山东地方鸡种、5个云南地方品种、藏鸡和白羽肉鸡专门化品系等19个品种/品系全基因组重测序数据为素材,通过群体分化指数分析后,提取MEAN_FAST≥0.65的SNP标记,进一步通过连锁不平衡分析提取独立SNP来缩减特征性SNP标记集合。随机选择6个品种/品系对该方法进行检验,结果表明,通过一次群体分化指数和连锁不平衡分析后进行位点筛选后,即可分别获得白羽肉鸡品系、京星黄鸡H系和京星黄鸡D2系的114、220和226个特征性SNPs位点,将目标品系与其它共18个代表性品种分开。对于在主成分和聚类分析中聚集在同一个分支的武定鸡和瓢鸡,通过该方法可分别获得204和178个特征性SNPs标记,将之与其它代表性品种分开。综上,通过本方法,可得到目标品种114~226个SNPs标记构成的集合,进一步利用主成分分析即可将目标品种/品系与其它代表性品种进行区分。该方法流程简便,获得的特征性SNP标记相对较少,有利于控制检测成本,可应用于地方品种或商业化品系的"分子身份证"构建,辅助种质资源保护和鉴定工作。

关键词: 鸡, 主成分分析, 群体分化指数分析, 连锁不平衡, 特征性SNP标记集合

Abstract: The purpose of this study was to establish a method to rapidly mine a few SNPs markers that can distinguish the target breeds or strains from other breeds or strains. The goal is to develop a technique for quickly mining the characteristic SNP markers set of chicken breeds or strains. The study used whole genome resequencing data of 19 breeds or strains, including Beijing yellow chicken, Jingxing yellow chicken, 7 Shandong local breeds, 5 Yunnan local breeds, Tibetan chicken, and the fast-growing white feather broiler terminal. After fixation indices analysis,SNP markers with MEAN_FAST ≥ 0.65 were extracted. The SNP markers set was further reduced by extracting independent SNP through linkage disequilibrium analysis. Six breeds or strains were chosen randomly to test this method. The results showed that, after loci screening by once fixation indices analysis and linkage disequilibrium analysis, the fast growing white feather broiler, Jingxing yellow chicken selective line H and Jingxing yellow chicken selective line D2 could be separated from other 18 representative breeds by 114, 220 and 226 SNPs, respectively; Wuding chicken and Piao chicken, which were clustered in one branch by principal component analysis and Neighbour Joining tree, could be separated from other representative breeds by 204 and 178 SNPs, respectively. Obtained the set of 114-226 SNPs markers, and that the target breeds or strains could be distinguished from other representative varieties by principal component analysis. The procedure is straightforward, and the quantity of SNP markers obtained is quite low, which helps for manage detection costs. It can be applied to construct the "molecular identity cards" of local variaties or commercial strairns to assist the protection and identification of germplasm resources.

Key words: chicken, principal component analysis, fixation indices analysis, linkage disequilibrium, characteristic SNP markers set

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