首页> 美国卫生研究院文献>Genetics >Least squares interval mapping of quantitative trait loci under the infinitesimal genetic model in outbred populations.
【2h】

Least squares interval mapping of quantitative trait loci under the infinitesimal genetic model in outbred populations.

机译:近亲群体无限小遗传模型下数量性状基因座的最小二乘区间作图。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Genetic marker and phenotypic data for a quantitative trait were simulated on 20 paternal half-sib families with 100 progeny to investigate properties of within-family-regression interval mapping of a postulated single quantitative trait locus (QTL) in a marker interval under the infinitesimal genetic model, which has been the basis of the application of quantitative genetics to genetic improvement programs, and to investigate use of the infinitesimal model as null hypothesis in testing for presence of a major QTL. Genetic effects on the marked chromosome were generated based on a major gene model, which simulated a central biallelic QTL, or based on 101 biallelic QTL of equal effect, which approximated the infinitesimal model. The marked chromosome contained 0, 3.3%, 13.3%, or 33.3% of genetic variance and heritability was 0.25 or 0.70. Under the polygenic model with 3.3% of genetic variance on the marked chromosome, which corresponds to the infinitesimal model for the bovine, significant QTL effects were found for individual families. Correlations between estimates of QTL effects and true chromosome substitution effects were 0.29 and 0.47 for heritabilities of 0.25 and 0.70 but up to 0.85 with 33.3% of polygenic variance on the marked chromosome. These results illustrate the potential of marker-assisted selection even under the infinitesimal genetic model. Power of tests for presence of QTL was substantially reduced when the polygenic model with 3.3% of genetic variance on the chromosome was used as a null hypothesis. The ability to determine whether genetic variance on a chromosome was contributed by a single QTL of major effect or a large number of QTL with minor effects, corresponding to the infinitesimal model, was limited.
机译:定量特征的遗传标记和表型数据在20个具有100个后代的父系半同胞家中进行了模拟,以研究无限小遗传条件下标记间隔中假定的单个数量性状基因座(QTL)的家庭回归区间作图的特性。该模型已成为定量遗传学在遗传改良计划中应用的基础,并研究了无穷小模型作为零假设在测试主要QTL存在中的用途。对标记染色体的遗传效应是根据主要基因模型(模拟中央双等位基因QTL)或基于101个等效的等位基因QTL(近似无穷小模型)产生的。标记的染色体包含0、3.3%,13.3%或33.3%的遗传变异,遗传力为0.25或0.70。在标记染色体上具有3.3%遗传变异的多基因模型(对应于牛的无穷小模型)下,发现单个家庭的显着QTL效应。遗传力0.25和0.70的QTL效应估计值与真实染色体替代效应之间的相关性分别为0.29和0.47,最高可达0.85,标记染色体上的多基因变异为33.3%。这些结果说明了即使在无限小遗传模型下,标记辅助选择的潜力。当使用在染色体上具有3.3%遗传变异的多基因模型作为无效假设时,QTL存在的测试能力大大降低。确定染色体上遗传变异是由单个QTL产生重大影响还是与大量QTL产生轻微影响(对应于无穷小模型)的能力受到限制。

著录项

  • 期刊名称 Genetics
  • 作者

    Z Liu; J C Dekkers;

  • 作者单位
  • 年(卷),期 1998(148),1
  • 年度 1998
  • 页码 495–505
  • 总页数 11
  • 原文格式 PDF
  • 正文语种
  • 中图分类 遗传学;
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号