Genetic diversity analysis and development of molecular markers for the identification of largemouth bass (Micropterus salmoides L.) based on whole-genome re-sequencing

被引:10
作者
Du, Jinxing [1 ]
Li, Shengjie [1 ]
Shao, Jiaqi [1 ]
Song, Hongmei [1 ]
Jiang, Peng [1 ]
Lei, Caixia [1 ]
Bai, Junjie [1 ]
Han, Linqiang [2 ]
机构
[1] Chinese Acad Fishery Sci, Pearl River Fisheries Res Inst, Key Lab Trop & Subtrop Fishery Resources Applicat, Minist Agr & Rural Affairs, Guangzhou, Peoples R China
[2] Guangdong Liangshi Aquat Seed Ind Co Ltd, Foshan, Peoples R China
关键词
largemouth bass; genetic diversity; germplasm identification; SNP; INDEL; MICROSATELLITE LOCI; FLORIDA; NORTHERN; DNA; HYBRID; AMPLIFICATION; FORMAT; F1;
D O I
10.3389/fgene.2022.936610
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Largemouth bass (Micropterus salmoides L.) is generally considered to comprise two subspecies, Florida bass (M. floridanus) and Northern Largemouth bass (M. salmoides), which have biological characteristic differences because of their geographical distribution. In this study, whole-genome re-sequencing was performed among 10 Florida and 10 Northern largemouth bass, respectively. In total, 999,793 SNPs and 227,797 InDels were finally identified, and 507,401 SNPs (50.75%) and 116,213 InDels (51.01%) were successfully mapped to annotated 18,629 genes and 14,060 genes, respectively. KEGG classification indicated that most of these genes were focused on the pathways including signal transduction, transport and catabolism, and endocrine system. Genetic diversity analysis indicated that Florida largemouth bass had higher genetic diversity than Northern largemouth bass, indicating that the germplasm quality of Northern largemouth bass had markedly reduced in China. To examine the accuracies of the identified markers, 23 SNPs and eight InDels (the insertions or deletions of more than 45 bp) were randomly selected and detected among Florida largemouth bass, Northern largemouth bass, and their F1 hybrids. The detection efficiencies of all the markers were higher than 95%; nineteen SNPs and three InDels could accurately distinguish the two subspecies and their F1 hybrids with 100% efficiencies. Moreover, the three InDel markers could clearly distinguish the two subspecies and their F1 hybrids with a PCR-based agarose gel electrophoresis. In conclusion, our study established a simple PCR-based method for the germplasm identification of largemouth bass, which will be useful in the germplasm protection, management, and hybridization breeding of largemouth bass.
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页数:11
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