用于对太平洋牡蛎进行高通量、低成本基因分型的扩增子面板。

IF 2.1 3区 生物学 Q3 GENETICS & HEREDITY
Ben J G Sutherland, Neil F Thompson, Liam B Surry, Krishna Reddy Gujjula, Claudio D Carrasco, Srinivas Chadaram, Spencer L Lunda, Christopher J Langdon, Amy M Chan, Curtis A Suttle, Timothy J Green
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引用次数: 0

摘要

由于个体繁殖成功率差异大、创始人效应和快速遗传漂移,保持养殖贝类的遗传多样性具有挑战性,但这对保持适应潜力和避免近亲繁殖抑制非常重要。为了支持养殖太平洋牡蛎(Crassostrea (Magallana) gigas)的育种管理和选择性繁殖,我们开发了一个扩增子面板,目标是 592 个基因组区域和 SNP 变异,平均每个染色体有 50 个扩增子。目标 SNP 是根据在加拿大不列颠哥伦比亚省的太平洋牡蛎种群中观察到的杂合度升高或分化情况选定的。使用来自加拿大温哥华岛育种计划的多代牡蛎(n = 181)和来自美国俄勒冈州软体动物繁殖计划(n = 136)的抗牡蛎疱疹病毒-1 家族,对亲本应用面板的使用进行了评估。利用在北半球各地采样的野生、归化、养殖或孵化牡蛎(n = 190)对种群特征进行了评估。技术复制显示基因型高度一致(97.5%;n = 68 个复制)。亲本分析发现了疑似的血统和样本处理错误,证明了该小组在育种计划中的质量控制价值。已鉴定出疑似无效等位基因,并发现这些等位基因在很大程度上取决于种群,这表明种群特异性变异会影响目标扩增。利用现有数据识别出了无效等位基因,而不需要血统信息,一旦去除无效等位基因,两个育种计划数据集的分配率分别提高到 93.0% 和 86.0%。此外,还提供了一个用于分析测序仪输出的扩增子序列数据的管道--amplitools。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An amplicon panel for high-throughput and low-cost genotyping of Pacific oyster.

Maintaining genetic diversity in cultured shellfish can be challenging due to high variance in individual reproductive success, founder effects, and rapid genetic drift, but is important to retain adaptive potential and avoid inbreeding depression. To support broodstock management and selective breeding in cultured Pacific oysters (Crassostrea (Magallana) gigas), we developed an amplicon panel targeting 592 genomic regions and SNP variants with an average of 50 amplicons per chromosome. Target SNPs were selected based on elevated observed heterozygosity or differentiation in Pacific oyster populations in British Columbia, Canada. The use of the panel for parentage applications was evaluated using multiple generations of oysters from a breeding program on Vancouver Island, Canada (n = 181) and families selected for Ostreid herpesvirus-1 resistance from the Molluscan Broodstock Program in Oregon, USA (n = 136). Population characterization was evaluated using wild, naturalized, farmed, or hatchery oysters sampled throughout the Northern Hemisphere (n = 189). Technical replicates showed high genotype concordance (97.5%; n = 68 replicates). Parentage analysis found suspected pedigree and sample handling errors, demonstrating the panel's value for quality control in breeding programs. Suspected null alleles were identified and found to be largely population dependent, suggesting population-specific variation impacting target amplification. Null alleles were identified using existing data without the need for pedigree information, and once they were removed, assignment rates increased to 93.0 and 86.0% of possible assignments in the two breeding program datasets. A pipeline for analyzing the amplicon sequence data from sequencer output, amplitools, is also provided.

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来源期刊
G3: Genes|Genomes|Genetics
G3: Genes|Genomes|Genetics GENETICS & HEREDITY-
CiteScore
5.10
自引率
3.80%
发文量
305
审稿时长
3-8 weeks
期刊介绍: G3: Genes, Genomes, Genetics provides a forum for the publication of high‐quality foundational research, particularly research that generates useful genetic and genomic information such as genome maps, single gene studies, genome‐wide association and QTL studies, as well as genome reports, mutant screens, and advances in methods and technology. The Editorial Board of G3 believes that rapid dissemination of these data is the necessary foundation for analysis that leads to mechanistic insights. G3, published by the Genetics Society of America, meets the critical and growing need of the genetics community for rapid review and publication of important results in all areas of genetics. G3 offers the opportunity to publish the puzzling finding or to present unpublished results that may not have been submitted for review and publication due to a perceived lack of a potential high-impact finding. G3 has earned the DOAJ Seal, which is a mark of certification for open access journals, awarded by DOAJ to journals that achieve a high level of openness, adhere to Best Practice and high publishing standards.
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