华北农学报 ›› 2023, Vol. 38 ›› Issue (S1): 437-443. doi: 10.7668/hbnxb.20193703

所属专题: 水产

• 畜牧·水产·兽医 • 上一篇    下一篇

大龙虎泡野生日本沼虾遗传多样性分析

兰若林1,2, 马文智2, 张立民2, 孙博2, 常玉梅2, 梁利群2   

  1. 1 大连海洋大学 水产与生命学院,辽宁 大连 116023
    2 中国水产科学研究院 黑龙江水产研究所,淡水鱼类育种国家地方联合工程实验室,农业农村部淡水水产生物技术与遗传育种重点实验室,黑龙江省特殊生境鱼类种质特性与抗逆育种重点实验室,黑龙江 哈尔滨 150070
  • 收稿日期:2023-05-19 出版日期:2023-12-28
  • 通讯作者:
    梁利群(1963—),女,黑龙江哈尔滨人,研究员,博士,博士生导师,主要从事鱼类抗逆分子遗传机理及基因工程育种研究。
  • 作者简介:

    兰若林(1999—),男,湖南醴陵人,在读硕士,主要从事虾类遗传育种研究。

  • 基金资助:
    国家重点研发计划课题(2019YFD0900405)

Genetic Diversity Analysis of Macrobrachium nipponense from Dalonghupao

LAN Ruolin1,2, MA Wenzhi2, ZHANG Limin2, SUN Bo2, CHANG Yumei2, LIANG Liqun2   

  1. 1 College of Fisheries and Life Science,Dalian Ocean University,Dalian 116023,China
    2 National and Local Joint Engineering Laboratory of Freshwater Fish Breeding;Key Laboratory of Freshwater Aquatic Biotechnology and Genetic Breeding,Ministry of Agriculture and Rural Affairs;Heilongjiang Province's Key Laboratory of Fish Stress Resistance Breeding and Germplasm Characteristics on Special Habitat,Heilongjiang River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Harbin 150070, China
  • Received:2023-05-19 Published:2023-12-28

摘要:

为了深入了解本地日本沼虾的遗传特性,为育种选育提供理论支撑,利用微卫星分子标记技术,对大龙虎泡日本沼虾进行遗传多样性比较分析。结果显示,12个微卫星位点均属于高多态性位点(PIC>0.5);太湖2号养殖群体的等位基因数为4~11,有效等位基因为3.686 4~7.480 5,观测杂合度为0.318 2~0.833 3,期望杂合度为0.744 9~0.884 8;各位点的多态性为0.691 9~0.851 7,属于高遗传多样性的群体。大龙虎泡野生群体等位基因数为1~2,有效等位基因为1.00 0 0~2.000 0,观测杂合度为0.000 0~1.000 0,期望杂合度为0.000 0~0.517 2,各位点的多态性为0.000 0~0.375 0,属于遗传多样性较低的群体。2个群体均有7个位点显著偏离Hardy-Weinberg平衡,大龙虎泡野生群体另出现3个位点无法进行Hardy-Weinberg平衡检验。太湖2号养殖群体的7个位点表现出来的是杂合子缺失,大龙虎泡野生群体的7个表现的是杂合子过剩。分子方差分析显示,有36.15%(P<0.01)的遗传变异来源于群体间,而63.85%(P<0.01)的变异来源于群体内。与太湖2号养殖群体的遗传相似度为0.276 9,遗传距离为1.284 3,这2个群体遗传相似度低,遗传距离远,存在很大的遗传差异。2个群体的遗传分化指数FST为0.361 53(P<0.01),遗传分化程度明显。种群遗传结构分析结果显示,最佳K值为3,说明这2个种群有3个可能的祖先。大龙虎泡野生群体遗传多样性水平较低,提示对大龙虎泡野生群体种质资源的保护刻不容缓。

关键词: 日本沼虾, 遗传多样性, 微卫星, 太湖2号, 分子标记

Abstract:

To learn more about the genetic characteristics of Macrobrachium nipponense and provide theoretical support for breeding selection,it used microsatellite molecular marking technology to compare the genetic diversity of Macrobrachium nipponense in Dalonghupao. The results showed that all 12 microsatellite loci were highly polymorphic loci (PIC>0.5). In the population of Taihu 2,the observed number of alleles ranged from 4 to 11,the effective number of alleles ranged from 3.686 4 to 7.480 5,the observed heterozygosity was 0.318 2—0.833 3,the expected heterozygosity was 0.744 9—0.884 8,the PIC of each locus was 0.691 9—0.851 7. The population of Taihu 2 was with high genetic diversity. In the population of Dalonghupao,the observed number of alleles ranged from 1—2,the effective number of alleles was 1.000 0—2.000 0,the observed heterozygosity was 0.000 0—1.000 0,the expected heterozygosity was 0.000 0—0.517 2,the PIC of each locus was 0.000 0—0.375 0. The population of Dalonghupao was with low genetic diversity. Seven loci in both populations deviated significantly from Hardy-Weinberg equilibrium,and three loci in the population of Dalonghupao could not be tested for Hardy-Weinberg equilibrium. Seven loci in the population of Taihu 2 showed heterozygous deletion,while seven loci in the population of Dalonghupao showed heterozygous excess. AMOVA analysis showed that 36.15% (P<0.01)of the total genetic variation was among populations and 63.85% (P<0.01)was among individuals. The genetic similarity between the population of Dalonghupao and the population of Taihu 2 was 0.276 9 and the genetic distance was 1.284 3,which showed that the genetic similarity between the two populations was low,and the genetic distance was far,and there were great genetic differences. The genetic differentiation index (FST)of the two populations was 0.361 53 (P<0.01),and the degree of genetic differentiation was obvious. The population genetic structure analysis showed an optimal K value of 3,indicating that the two populations had three possible ancestors. The level of genetic diversity of Dalonghupao wild population was low,which prompting us to protect the germplasm resources of the population of Dalonghupao.

Key words: Macrobrachium nipponense, Genetic diversity, Microsatellite, Taihu 2, Molecular marker

引用本文

兰若林, 马文智, 张立民, 孙博, 常玉梅, 梁利群. 大龙虎泡野生日本沼虾遗传多样性分析[J]. 华北农学报, 2023, 38(S1): 437-443. doi: 10.7668/hbnxb.20193703.

LAN Ruolin, MA Wenzhi, ZHANG Limin, SUN Bo, CHANG Yumei, LIANG Liqun. Genetic Diversity Analysis of Macrobrachium nipponense from Dalonghupao[J]. Acta Agriculturae Boreali-Sinica, 2023, 38(S1): 437-443. doi: 10.7668/hbnxb.20193703.

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