《中国畜牧兽医》 ›› 2018, Vol. 45 ›› Issue (3): 730-737.doi: 10.16431/j.cnki.1671-7236.2018.03.022

• 遗传繁育 • 上一篇    下一篇

静原鸡ELOVL2基因遗传多态性研究

母童1, 顾亚玲1, 赵平2, 冯小芳1, 陈佳萍1, 陈亚飞1, 刘丽元1, 蒋秋斐1, 张娟1   

  1. 1. 宁夏大学农学院, 银川 750021;
    2. 彭阳县畜牧技术推广服务中心, 固原 756500
  • 收稿日期:2017-09-15 出版日期:2018-03-20 发布日期:2018-03-22
  • 通讯作者: 张娟 E-mail:zhangjkathy@126.com
  • 作者简介:母童(1995-),男,回族,宁夏银川人,硕士生,研究方向:动物遗传育种与繁殖,E-mail:1227415848@qq.com
  • 基金资助:

    2017年自治区级大学生创新创业训练计划项目——静原鸡ELOVL5基因的多态性研究(Q201710749050)

Study on Polymorphism of ELOVL2 Gene in Jingyuan Chicken

MU Tong1, GU Yaling1, ZHAO Ping2, FENG Xiaofang1, CHEN Jiaping1, CHEN Yafei1, LIU Liyuan1, JIANG Qiufei1, ZHANG Juan1   

  1. 1. College of Agriculture, Ningxia University, Yinchuan 750021, China;
    2. Animal Husbandry and Technology Promotion Service Center of Pengyang County, Guyuan 756500, China
  • Received:2017-09-15 Online:2018-03-20 Published:2018-03-22

摘要:

为了探讨静原鸡极长链脂肪酸延伸酶蛋白2(elongation of very-long-chain fatty acids 2,ELOVL2)基因的遗传特性,确定核苷酸的变异位点,本研究采用PCR-SSCP及DNA测序技术对静原鸡ELOVL2基因进行多态性检测。结果显示,静原鸡ELOVL2基因外显子6无多态性,内含子2和6呈中度多态。在ELOVL2基因内含子2扩增片段上共检测到5种基因型:A2A2、B2B2、C2C2、D2D2和A2C2,4种等位基因:A2、B2、C2和D2,其中A2为优势等位基因(0.62),A2A2基因型为优势基因型(0.54);3个SNPs位点:g.63372228+4918G > A的转换、g.63372228+5024T > C的转换和g.63372228+4928C > A的颠换。在E2e6I6扩增片段上共检测到3种基因型:A1A1、B1B1和A1B1,2种等位基因:A1和B1,其中A1为优势等位基因(0.67),A1A1基因型为优势基因型(0.54),等位基因B1存在g.63388000+748G > C的颠换。群体遗传学分析发现,静原鸡ELOVL2基因内含子2、6遗传纯合度均较高,且偏离了Hardy-Weinberg平衡(P < 0.05)。本研究结果表明,静原鸡ELOVL2基因内含子2和6序列突变较高,且呈中度多态,表现出纯合子优势,外显子6上无突变。

关键词: 静原鸡; ELOVL2基因; 多态性

Abstract:

In order to study the genetic characteristics and nucleotide polymorphism sites of elongation of very-long-chain fatty acids 2 (ELOVL2) gene in Jingyuan chicken,the polymorphisms of ELOVL2 gene were detected by polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) and DNA sequence.The results showed that there was no polymorphism of ELOVL2 gene exon 6,there were moderate polymorphism of introns 2 and 6 in Jingyuan chicken.The total of 5 genotypes(A2A2,B2B2,C2C2,D2D2 and A2C2),4 alleles(A2,B2,C2 and D2) and 3 SNPs loci were detected on the intron 2 amplified fragment of ELOVL2 gene.The 3 SNPs were g.63372228+4918G > A transformation,g.63372228+5024T > C transformation and g.63372228+4928C > A transversion.A2 was the dominant allele (0.62),and A2A2 was the dominant genotype (0.54).The total of 3 genotypes (A1A1,B1B1 and A1B1) and 2 alleles (A1 and B1) were detected on E2e6I6 amplified fragments.A1 was the dominant allele (0.67),A1A1 was the dominant genotype (0.54),and only allele B1 had a g.63388000+748G > C transversion.Population genetics analysis showed that genetic homozygosity of ELOVL2 gene introns 2 and 6 in Jingyuan chicken were higher and deviation from Hardy-Weinberg equilibrium (P < 0.05).The results showed that the mutations of the ELOVL2 gene introns 2 and 6 in the Jingyuan chicken were high,which were moderate polymorphism,showing the homozygous advantage and no mutation on the exon 6.

Key words: Jingyuan chicken; ELOVL2 gene; polymorphism

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