《中国畜牧兽医》 ›› 2018, Vol. 45 ›› Issue (8): 2236-2246.doi: 10.16431/j.cnki.1671-7236.2018.08.024

• 遗传繁育 • 上一篇    下一篇

6个绵羊群体BMP15、GDF9基因多态性分析

吴翠玲1,2, 宗兴龙1,2, 赵卓1, 赵云辉1, 翟博1, 张明新1, 王春昕1   

  1. 1. 吉林省农业科学院, 公主岭 136100;
    2. 吉林农业大学, 长春 130000
  • 收稿日期:2018-01-02 出版日期:2018-08-20 发布日期:2018-08-15
  • 通讯作者: 张明新, 王春昕 E-mail:zmxin@163.com;Tracywang@cau.edu.cn
  • 作者简介:吴翠玲(1994-),女,新疆库尔勒人,硕士生,研究方向:动物遗传育种与繁殖,E-mail:m13139696833@163.com
  • 基金资助:

    国家绒毛用羊产业技术体系(CARS-39-17);吉林省高纺细羊毛生产科技创新中心(20170623003TC);吉林省肉羊产业技术体系(2016041);吉林省农业科学院创新工程(CXGC2017ZY001、C6215000217、C7208000203)

Genetic Polymorphism Analysis of BMP15 and GDF9 Genes in Six Sheep Breeds

WU Cuiling1,2, ZONG Xinglong1,2, ZHAO Zhuo1, ZHAO Yunhui1, ZHAI Bo1, ZHANG Mingxin1, WANG Chunxin1   

  1. 1. Jilin Academy of Agricultural Sciences, Gongzhuling 136100, China;
    2. Jilin Agricultural University, Changchun 130000, China
  • Received:2018-01-02 Online:2018-08-20 Published:2018-08-15

摘要:

本研究旨在检测新吉细毛羊、中国美利奴羊(无角型)、东北细毛羊、杜×寒杂交羊(F1)、杜×寒杂交羊(F3)、白头杜泊羊6个绵羊群体骨形态发生蛋白15(bone morphogenetic protein 15,BMP15)、生长分化因子9(growth differentiation factor 9,GDF9)基因的多态性,为绵羊繁殖力的标记辅助选择和育种提供理论依据。以6个绵羊群体共378只个体为研究对象,利用PCR-SSCP技术检测BMP15、GDF9基因多态性;用DNAStar软件与I-TASSER软件预测蛋白质二级结构和三级结构;计算基因频率、基因型频率、Hardy-Weinberg平衡、杂合度(He)、纯合度(Ho)、有效等位基因数(Ne)和多态信息含量(PIC)。运用GraphPad Prism 6软件对新吉细毛羊群体BMP15基因多态性与产羔数进行相关性分析。结果显示,BMP15基因P1引物扩增片段存在多态性,6个群体共呈现3种基因型:AA、AC、CC,该突变为BMP15基因外显子1上58-60 bp 3个碱基(CTT)缺失,新吉细毛羊、杜×寒杂交羊(F3)、白头杜泊羊的χ2值均达到显著水平,处于Hardy-Weinberg不平衡状态,不同基因型间新吉细毛羊平均产羔数差异均不显著(P>0.05);GDF9基因P2引物扩增片段存在多态性,6个群体共呈现3种基因型:DD、DE、EE,其中新吉细毛羊仅有1种基因型:DD,该突变为GDF9基因外显子2上477 bp处T→C的转换,该突变未导致氨基酸的改变,除新吉细毛羊外其余5个群体χ2值均未达到显著水平,处于Hardy-Weinberg平衡状态,说明GDF9基因T477C突变不能作为新吉细毛羊多胎性状遗传标记位点。

关键词: 绵羊; BMP15基因; GDF9基因; 多态性

Abstract:

This study was aimed to detect the gene polymorphism of bone morphogenetic protein 15(BMP15) and growth differentiation factor 9 (GDF9) genes in Xinji Fine-wool sheep,Northeast Fine-wool sheep,Chinese Merino(Mulley type) sheep,Dorper×Han crossbred sheep (F1),Dorper×Han crossbred sheep (F3) and White Dorper sheep,which would provide a theoretical basis for marker-assisted selection and breeding for prolificacy in sheep.A total of 378 individuals from six sheep breeds were used to study the polymorphism of BMP15 and GDF9 genes by PCR-SSCP.Secondary structure and tertiary structure of proteins were predicted using DNAStar and I-TASSER.Gene frequency,genotype frequency,Hardy-Weinberg equilibrium,heterozygosity (He),homozygous (Ho),number of effective alleles (Ne) and polymorphic information content (PIC) were calculated.The correlation was analyzed between BMP15 gene polymorphism and litter size in Xinji Fine-wool sheep by GraphPad Prism 6 software.The results showed that the polymorphism was found in P1 primer amplification fragment of BMP15 gene,there were three genotypes of AA,AC and CC in six breeds.This mutation was a 58-60 bp (CTT) deletion in exon 1 of BMP15 gene.According to χ2 test,Xinji Fine-wool sheep,Dorper×Han crossbred sheep (F3) and White Dorper sheep were not in Hardy-Weinberg equilibrium.There was no significant difference in the average litter size of different genotypes in Xinji Fine-wool sheep (P>0.05).The polymorphism was found in P2 primer amplification fragment of GDF9 gene.There were three genotypes of DD,DE and EE in six breeds,and there were only one genotype in Xinji Fine-wool sheep.This mutation was a T→C conversion at 477 bp on GDF9 gene exon 2 which didn't lead to amino acid change.According to χ2 test,five breeds (except for Xinji Fine-wool sheep) were in Hardy-Weinberg equilibrium.The results indicated that the GDF9 gene T477C mutation couldn't be used as a genetic marker for multiple fetal traits in Xinji Fine-wool sheep.

Key words: sheep; BMP15 gene; GDF9 gene; polymorphism

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