Development and Evaluation of High-Density SNP Arrays for the Eastern Oyster Crassostrea virginica

被引:16
|
作者
Guo, Ximing [1 ]
Puritz, Jonathan B. [2 ]
Wang, Zhenwei [1 ]
Proestou, Dina [3 ]
Allen, Standish, Jr. [4 ]
Small, Jessica [4 ]
Verbyla, Klara [5 ]
Zhao, Honggang [6 ]
Haggard, Jaime [1 ]
Chriss, Noah [1 ]
Zeng, Dan [1 ]
Lundgren, Kathryn [3 ]
Allam, Bassem [7 ]
Bushek, David [1 ]
Gomez-Chiarri, Marta [8 ]
Hare, Matthew [6 ]
Hollenbeck, Christopher [9 ]
La Peyre, Jerome [10 ]
Liu, Ming [11 ]
Lotterhos, Katie E. [12 ]
Plough, Louis [13 ]
Rawson, Paul [14 ]
Rikard, Scott [15 ]
Saillant, Eric [16 ]
Varney, Robin [17 ]
Wikfors, Gary [18 ]
Wilbur, Ami [17 ]
机构
[1] Rutgers State Univ, Haskin Shellfish Res Lab, 6959 Miller Ave, Port Norris, NJ 08349 USA
[2] Univ Rhode Isl, Dept Biol Sci, 120 Flagg Rd, Kingston, RI 02881 USA
[3] ARS, USDA, NCWMAC Shellfish Genet Lab, 120 Flagg Rd, Kingston, RI 02881 USA
[4] Virginia Inst Marine Sci, 1375 Greate Rd, Gloucester Point, VA 23062 USA
[5] CSIRO, Canberra, ACT 2601, Australia
[6] Cornell Univ, Dept Nat Resources & Environm, Ithaca, NY 14853 USA
[7] SUNY Stony Brook, Sch Marine & Atmospher Sci, Stony Brook, NY 11794 USA
[8] Univ Rhode Isl, Dept Fisheries Anim & Vet Sci, 120 Flagg Rd, Kingston, RI 02881 USA
[9] Texas A&M Univ, Texas A&M AgriLife Res, 6300 Ocean Dr Unit 5892, Corpus Christi, TX 78412 USA
[10] Louisiana State Univ, Agr Ctr, Sch Anim Sci, 201 Anim & Food Sci Lab Bldg,Forestry Lane, Baton Rouge, LA 70803 USA
[11] Morgan State Univ, Patuxent Environm & Aquat Res Lab, 10545 Mackall Rd, St Leonard, MD 20685 USA
[12] Northeastern Marine Sci Ctr, 430 Nahant Rd, Nahant, MA 01908 USA
[13] Univ Maryland, Horn Point Lab, 5745 Lovers Lane, Cambridge, MD 21613 USA
[14] Univ Maine, Sch Marine Sci, 5751 Murray Hall, Orono, ME 04469 USA
[15] Auburn Univ, Shellfish Lab, Sch Fisheries Aquaculture & Aquat Sci, 150 Agassiz St, Dauphin Isl, AL 36528 USA
[16] Univ Southern Mississippi, Sch Ocean Sci & Engn, 103 McIlwain Dr, Ocean Springs, MS 39564 USA
[17] Univ N Carolina, Shellfish Res Hatchery, 5600 Marvin K Moss Ln, Wilmington, NC 28409 USA
[18] NOAA Fisheries, Milford CT Lab, 212 Rogers Ave, Milford, CT 06460 USA
基金
美国海洋和大气管理局;
关键词
Oyster aquaculture; Genomic selection; Single-nucleotide polymorphism; SNP array; Genome-wide association study; Copy number variation; EST-SSR MARKERS; PACIFIC OYSTER; NULL ALLELES; HETEROZYGOTE DEFICIENCIES; MITOCHONDRIAL-DNA; GENETIC LOAD; SELECTION; RESTORATION; PERFORMANCE; INFERENCE;
D O I
10.1007/s10126-022-10191-3
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The eastern oyster Crassostrea virginica is a major aquaculture species for the USA. The sustainable development of eastern oyster aquaculture depends upon the continued improvement of cultured stocks through advanced breeding technologies. The Eastern Oyster Breeding Consortium (EOBC) was formed to advance the genetics and breeding of the eastern oyster. To facilitate efficient genotyping needed for genomic studies and selection, the consortium developed two single-nucleotide polymorphism (SNP) arrays for the eastern oyster: one screening array with 566K SNPs and one breeders' array with 66K SNPs. The 566K screening array was developed based on whole-genome resequencing data from 292 oysters from Atlantic and Gulf of Mexico populations; it contains 566,262 SNPs including 47K from protein-coding genes with a marker conversion rate of 48.34%. The 66K array was developed using best-performing SNPs from the screening array, which contained 65,893 oyster SNPs including 22,984 genic markers with a calling rate of 99.34%, a concordance rate of 99.81%, and a much-improved marker conversion rate of 92.04%. Null alleles attributable to large indels were found in 13.1% of the SNPs, suggesting that copy number variation is pervasive. Both arrays provided easy identification and separation of selected stocks from wild progenitor populations. The arrays contain 31 mitochondrial SNPs that allowed unambiguous identification of Gulf mitochondrial genotypes in some Atlantic populations. The arrays also contain 756 probes from 13 oyster and human pathogens for possible detection. Our results show that marker conversion rate is low in high polymorphism species and that the two-step process of array development can greatly improve array performance. The two arrays will advance genomic research and accelerate genetic improvement of the eastern oyster by delineating genetic architecture of production traits and enabling genomic selection. The arrays also may be used to monitor pedigree and inbreeding, identify selected stocks and their introgression into wild populations, and assess the success of oyster restoration.
引用
收藏
页码:174 / 191
页数:18
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