为什么有用很少有用。

IF 2.1 3区 生物学 Q3 GENETICS & HEREDITY G3: Genes|Genomes|Genetics Pub Date : 2024-12-24 DOI:10.1093/g3journal/jkae296
Fangyi Wang, Mitchell J Feldmann, Daniel E Runcie
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引用次数: 0

摘要

配偶选择在育种计划中起着重要作用。有用性标准的提出是为了改进配偶选择,结合了杂交后代的平均和标准偏差的信息,特别是在可能有大家庭的无性繁殖物种中。预测杂交的平均值通常比预测标准偏差更容易,特别是在等位基因连锁未知且需要分阶段的远交种中。在这项研究中,我们开发了一种从可能亲本系的未分期基因型数据估计分期准确性的方法,并评估准确性是否足以预测可能杂交的家庭标准偏差。我们使用了跨越广泛遗传结构的模拟,并使用了来自真实草莓育种群体的基因型来评估可以准确预测有用性的条件。我们发现,在高度精确的计算相位下,预测潜在杂交产量的家族标准差和有用性标准优于仅在高选择强度和高遗传力以及QTL数量较少的情况下根据预测的家族均值进行简单选择。然而,即使这样,从使用家庭有用性中获得的收益也是很小的。
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Why usefulness is rarely useful.

Mate selection plays an important role in breeding programs. The Usefulness Criterion was proposed to improve mate selection, combining information on both the mean and standard deviation of the potential offspring of a cross, particularly in clonally propagated species where large family sizes are possible. Predicting the mean value of a cross is generally easier than predicting the standard deviation, especially in outbred species when the linkage of alleles is unknown and phasing is required. In this study, we developed a method for estimating phasing accuracy from unphased genotype data on possible parental lines and evaluated whether the accuracy was sufficient to predict family standard deviations of possible crosses. We used simulations spanning a wide range of genetic architectures and used genotypes from a real strawberry breeding population to evaluate the conditions when usefulness could be accurately predicted. We found that with highly accurate computational phasing, predicting family standard deviations and usefulness criteria for potential crosses yields benefit over simply selecting crosses based on predicted family means only at high selection intensity and high heritability and with small numbers of QTL. However, even then the gain from using the family usefulness is small.

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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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