Silva Joseane Padilha da, Caetano Alexandre Rodrigues
Embrapa Recursos Genéticos e Biotecnologia, Parque Estação Biológica, Brasília, DF, Brazil.
Genet Mol Biol. 2020 Aug 21;43(3):e20190324. doi: 10.1590/1678-4685-gmb-2019-0324.
Cross-species hybridizations have been extensively used to generate animals and plants better suited for draft and food and fiber production since Roman times, and are still important in current agricultural practices with growing uses especially in aquaculture. Diagnostic tools based on marker panels with sufficient numbers of markers for accurate identification of cross-species hybrid individuals from intercrossed and backcrossed populations are increasingly necessary for practical, accurate species-purity certification and management of commercial broodstocks. Minimal numbers of di-allelic markers with species-specific alleles required to accurately identify hybrid individuals in intercrossed and advanced backcrossed populations were estimated using power analysis, and ranged from 5 to 191 (α = .05), and from 7 to 293 (α = .01), considering backcross 1 (BC1) to BC6 populations, respectively. Numbers of markers required for accurate hybrid identification observed in simulated BC1 to BC6 populations ranged from 5 to 1,131 and 7 to 8,065, considering error rates ≤ 5% and ≤ 1%, respectively. Estimated and observed numbers of diagnostic markers required for accurate hybrid identification up to four generations of backcrossing fall within practical operational limits of most commercial platforms currently available for genotyping low-density SNP marker panels. Therefore, cost-effective assay panels could be developed to provide practical tools for accurate species-purity certification.
自罗马时代以来,跨物种杂交就被广泛用于培育更适合役用、粮食和纤维生产的动植物,并且在当前的农业实践中仍然很重要,尤其是在水产养殖中的应用日益增加。对于商业亲鱼的实际、准确的物种纯度认证和管理而言,基于具有足够数量标记的标记面板的诊断工具对于从杂交和回交群体中准确识别跨物种杂交个体越来越必要。使用功效分析估计了在杂交和高级回交群体中准确识别杂交个体所需的具有物种特异性等位基因的双等位基因标记的最小数量,分别考虑回交1(BC1)到BC6群体,范围为5至191(α = 0.05),以及7至293(α = 0.01)。考虑到错误率分别≤5%和≤1%,在模拟的BC1至BC6群体中观察到的准确杂交鉴定所需的标记数量范围为5至1131和7至8065。在多达四代回交中准确杂交鉴定所需的诊断标记的估计数量和观察数量都在目前大多数用于低密度SNP标记面板基因分型的商业平台的实际操作范围内。因此,可以开发具有成本效益的检测面板,以提供用于准确物种纯度认证的实用工具。