• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

多亲本群体中 QTL 等位基因多样性对 QTL 检测的影响:甜菜的模拟研究。

The influence of QTL allelic diversity on QTL detection in multi-parent populations: a simulation study in sugar beet.

机构信息

Biometris, Wageningen University and research Center, P.O Box 100, Wageningen, 6700AC, The Netherlands.

KWS SAAT SE, Einbeck, Germany.

出版信息

BMC Genom Data. 2021 Feb 3;22(1):4. doi: 10.1186/s12863-021-00960-9.

DOI:10.1186/s12863-021-00960-9
PMID:33568071
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7860181/
Abstract

BACKGROUND

Multi-parent populations (MPPs) are important resources for studying plant genetic architecture and detecting quantitative trait loci (QTLs). In MPPs, the QTL effects can show various levels of allelic diversity, which can be an important factor influencing the detection of QTLs. In MPPs, the allelic effects can be more or less specific. They can depend on an ancestor, a parent or the combination of parents in a cross. In this paper, we evaluated the effect of QTL allelic diversity on the QTL detection power in MPPs.

RESULTS

We simulated: a) cross-specific QTLs; b) parental and ancestral QTLs; and c) bi-allelic QTLs. Inspired by a real application in sugar beet, we tested different MPP designs (diallel, chessboard, factorial, and NAM) derived from five or nine parents to explore the ability to sample genetic diversity and detect QTLs. Using a fixed total population size, the QTL detection power was larger in MPPs with fewer but larger crosses derived from a reduced number of parents. The use of a larger set of parents was useful to detect rare alleles with a large phenotypic effect. The benefit of using a larger set of parents was however conditioned on an increase of the total population size. We also determined empirical confidence intervals for QTL location to compare the resolution of different designs. For QTLs representing 6% of the phenotypic variation, using 1600 F offspring individuals, we found average 95% confidence intervals over different designs of 49 and 25 cM for cross-specific and bi-allelic QTLs, respectively.

CONCLUSIONS

MPPs derived from less parents with few but large crosses generally increased the QTL detection power. Using a larger set of parents to cover a wider genetic diversity can be useful to detect QTLs with a reduced minor allele frequency when the QTL effect is large and when the total population size is increased.

摘要

背景

多亲群体(MPP)是研究植物遗传结构和检测数量性状位点(QTL)的重要资源。在 MPP 中,QTL 效应可以表现出各种水平的等位基因多样性,这可能是影响 QTL 检测的一个重要因素。在 MPP 中,等位基因效应可以或多或少地具有特异性。它们可以依赖于一个祖先、一个亲本或杂交亲本的组合。在本文中,我们评估了 QTL 等位基因多样性对 MPP 中 QTL 检测能力的影响。

结果

我们模拟了:a)交叉特异性 QTL;b)亲本和祖先 QTL;c)双等位基因 QTL。受甜菜实际应用的启发,我们测试了来自 5 个或 9 个亲本的不同 MPP 设计(双列杂交、棋盘设计、析因设计和 NAM),以探索对遗传多样性进行采样和检测 QTL 的能力。在固定的总群体大小下,来自较少亲本但更大杂交的 MPP 具有更大的 QTL 检测能力,这些亲本数量减少了。使用更大的亲本集有助于检测具有较大表型效应的稀有等位基因。然而,使用更大的亲本集的好处取决于总群体大小的增加。我们还确定了 QTL 位置的经验置信区间,以比较不同设计的分辨率。对于代表 6%表型变异的 QTL,使用 1600 个 F 后代个体,我们发现不同设计的平均 95%置信区间分别为交叉特异性和双等位基因 QTL 的 49 和 25cM。

结论

来自较少亲本但具有较少但较大杂交的 MPP 通常会增加 QTL 检测能力。使用更大的亲本集来覆盖更广泛的遗传多样性,可以在 QTL 效应较大且总群体大小增加时,用于检测等位基因频率较低但 QTL 效应较小的 QTL。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ace/7860181/e472f51eea80/12863_2021_960_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ace/7860181/5f977acfdd9b/12863_2021_960_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ace/7860181/d5567242d83c/12863_2021_960_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ace/7860181/1c70b7686d76/12863_2021_960_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ace/7860181/d900d5fa17d2/12863_2021_960_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ace/7860181/aeb65f3b2200/12863_2021_960_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ace/7860181/e472f51eea80/12863_2021_960_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ace/7860181/5f977acfdd9b/12863_2021_960_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ace/7860181/d5567242d83c/12863_2021_960_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ace/7860181/1c70b7686d76/12863_2021_960_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ace/7860181/d900d5fa17d2/12863_2021_960_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ace/7860181/aeb65f3b2200/12863_2021_960_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ace/7860181/e472f51eea80/12863_2021_960_Fig6_HTML.jpg

相似文献

1
The influence of QTL allelic diversity on QTL detection in multi-parent populations: a simulation study in sugar beet.多亲本群体中 QTL 等位基因多样性对 QTL 检测的影响:甜菜的模拟研究。
BMC Genom Data. 2021 Feb 3;22(1):4. doi: 10.1186/s12863-021-00960-9.
2
How do the type of QTL effect and the form of the residual term influence QTL detection in multi-parent populations? A case study in the maize EU-NAM population.数量性状基因座(QTL)效应类型和残差项形式如何影响多亲本群体中的QTL检测?以玉米欧盟嵌套关联作图群体(EU-NAM)为例的研究。
Theor Appl Genet. 2017 Aug;130(8):1753-1764. doi: 10.1007/s00122-017-2923-3. Epub 2017 May 25.
3
An IBD-based mixed model approach for QTL mapping in multiparental populations.基于 IBD 的多亲本群体 QTL 作图的混合模型方法。
Theor Appl Genet. 2021 Nov;134(11):3643-3660. doi: 10.1007/s00122-021-03919-7. Epub 2021 Aug 3.
4
Multi-parental fungal mapping population study to detect genomic regions associated with Pyrenophora teres f. teres virulence.多亲本品系真菌作图群体研究,以检测与禾谷镰刀菌禾谷专化型毒性相关的基因组区域。
Sci Rep. 2023 Jun 16;13(1):9804. doi: 10.1038/s41598-023-36963-y.
5
Effect of advanced intercrossing on genome structure and on the power to detect linked quantitative trait loci in a multi-parent population: a simulation study in rice.高级杂交对多亲本群体基因组结构及检测连锁数量性状位点能力的影响:水稻模拟研究
BMC Genet. 2014 Apr 27;15:50. doi: 10.1186/1471-2156-15-50.
6
Modeling QTL-by-environment interactions for multi-parent populations.多亲群体数量性状基因座与环境互作的建模
Front Plant Sci. 2024 Jul 31;15:1410851. doi: 10.3389/fpls.2024.1410851. eCollection 2024.
7
A multi-locus linear mixed model methodology for detecting small-effect QTLs for quantitative traits in MAGIC, NAM, and ROAM populations.一种用于在多亲本高级世代互交群体(MAGIC)、嵌套关联作图群体(NAM)和随机家系高级世代互交群体(ROAM)中检测数量性状小效应数量性状基因座(QTL)的多位点线性混合模型方法。
Comput Struct Biotechnol J. 2023 Mar 15;21:2241-2252. doi: 10.1016/j.csbj.2023.03.022. eCollection 2023.
8
Discovery of interesting new polymorphisms in a sugar beet (elite [Formula: see text] exotic) progeny by comparison with an elite panel.通过与一个精英面板比较,在甜菜(优秀的[公式:见正文]外来)后代中发现有趣的新多态性。
Theor Appl Genet. 2019 Nov;132(11):3063-3078. doi: 10.1007/s00122-019-03406-0. Epub 2019 Sep 4.
9
Multiallelic models for QTL mapping in diverse polyploid populations.多等位基因模型在不同多倍体群体中的 QTL 定位。
BMC Bioinformatics. 2022 Feb 14;23(1):67. doi: 10.1186/s12859-022-04607-z.
10
QTL analysis of high thermotolerance with superior and downgraded parental yeast strains reveals new minor QTLs and converges on novel causative alleles involved in RNA processing.利用具有较高和较低亲本酵母菌株的 QTL 分析揭示了新的次要 QTL,并集中在涉及 RNA 处理的新的因果等位基因上。
PLoS Genet. 2013;9(8):e1003693. doi: 10.1371/journal.pgen.1003693. Epub 2013 Aug 15.

引用本文的文献

1
Deciphering the genetic basis of agronomic, yield, and nutritional traits in rice (Oryza sativa L.) using a saturated GBS-based SNP linkage map.利用基于饱和 GBS 的 SNP 连锁图谱解析水稻农艺、产量和营养性状的遗传基础。
Sci Rep. 2024 Aug 4;14(1):18024. doi: 10.1038/s41598-024-67543-3.
2
Characterization of adaptation mechanisms in sorghum using a multireference back-cross nested association mapping design and envirotyping.利用多参考回交嵌套关联作图设计和环境鉴定研究高粱的适应机制。
Genetics. 2024 Apr 3;226(4). doi: 10.1093/genetics/iyae003.
3
A multi-locus linear mixed model methodology for detecting small-effect QTLs for quantitative traits in MAGIC, NAM, and ROAM populations.

本文引用的文献

1
How do the type of QTL effect and the form of the residual term influence QTL detection in multi-parent populations? A case study in the maize EU-NAM population.数量性状基因座(QTL)效应类型和残差项形式如何影响多亲本群体中的QTL检测?以玉米欧盟嵌套关联作图群体(EU-NAM)为例的研究。
Theor Appl Genet. 2017 Aug;130(8):1753-1764. doi: 10.1007/s00122-017-2923-3. Epub 2017 May 25.
2
Comparison of statistical models for nested association mapping in rapeseed (Brassica napus L.) through computer simulations.通过计算机模拟对油菜(甘蓝型油菜)嵌套关联作图统计模型的比较。
BMC Plant Biol. 2016 Jan 25;16:26. doi: 10.1186/s12870-016-0707-6.
3
一种用于在多亲本高级世代互交群体(MAGIC)、嵌套关联作图群体(NAM)和随机家系高级世代互交群体(ROAM)中检测数量性状小效应数量性状基因座(QTL)的多位点线性混合模型方法。
Comput Struct Biotechnol J. 2023 Mar 15;21:2241-2252. doi: 10.1016/j.csbj.2023.03.022. eCollection 2023.
4
The double round-robin population unravels the genetic architecture of grain size in barley.双轮群体揭示了大麦粒大小的遗传结构。
J Exp Bot. 2022 Dec 8;73(22):7344-7361. doi: 10.1093/jxb/erac369.
5
Analysis of historical selection in winter wheat.冬小麦历史选择分析。
Theor Appl Genet. 2022 Sep;135(9):3005-3023. doi: 10.1007/s00122-022-04163-3. Epub 2022 Jul 21.
6
Multiallelic models for QTL mapping in diverse polyploid populations.多等位基因模型在不同多倍体群体中的 QTL 定位。
BMC Bioinformatics. 2022 Feb 14;23(1):67. doi: 10.1186/s12859-022-04607-z.
7
Physical Mapping of QTL in Four Spring Wheat Populations under Conventional and Organic Management Systems. I. Earliness.常规和有机管理系统下四个春小麦群体中数量性状位点的物理图谱。I. 早熟性。
Plants (Basel). 2021 Apr 23;10(5):853. doi: 10.3390/plants10050853.
8
Multi-parent populations in crops: a toolbox integrating genomics and genetic mapping with breeding.作物多亲种群:整合基因组学和遗传图谱与育种的工具包。
Heredity (Edinb). 2020 Dec;125(6):396-416. doi: 10.1038/s41437-020-0336-6. Epub 2020 Jul 3.
Choice of models for QTL mapping with multiple families and design of the training set for prediction of Fusarium resistance traits in maize.
用于玉米多个家系数量性状位点(QTL)定位的模型选择以及预测镰刀菌抗性性状的训练集设计。
Theor Appl Genet. 2016 Feb;129(2):431-44. doi: 10.1007/s00122-015-2637-3. Epub 2015 Dec 10.
4
Allele mining and enhanced genetic recombination for rice breeding.挖掘等位基因和增强遗传重组在水稻育种中的应用。
Rice (N Y). 2015 Dec;8(1):34. doi: 10.1186/s12284-015-0069-y. Epub 2015 Nov 25.
5
Linkage disequilibrium with linkage analysis of multiline crosses reveals different multiallelic QTL for hybrid performance in the flint and dent heterotic groups of maize.通过多系杂交的连锁分析进行连锁不平衡分析,揭示了玉米硬粒型和马齿型杂种优势群中杂种表现的不同多等位基因QTL。
Genetics. 2014 Dec;198(4):1717-34. doi: 10.1534/genetics.114.169367. Epub 2014 Sep 29.
6
Clusthaplo: a plug-in for MCQTL to enhance QTL detection using ancestral alleles in multi-cross design.Clusthaplo:一种用于MCQTL的插件,可在多杂交设计中利用祖先等位基因增强QTL检测。
Theor Appl Genet. 2014 Apr;127(4):921-33. doi: 10.1007/s00122-014-2267-1. Epub 2014 Jan 31.
7
Intraspecific variation of recombination rate in maize.玉米重组率的种内变异
Genome Biol. 2013;14(9):R103. doi: 10.1186/gb-2013-14-9-r103.
8
Optimum design of family structure and allocation of resources in association mapping with lines from multiple crosses.多杂交系关联作图中家庭结构的最优化设计和资源分配。
Heredity (Edinb). 2013 Jan;110(1):71-9. doi: 10.1038/hdy.2012.63. Epub 2012 Oct 10.
9
Mapping QTL for agronomic traits in breeding populations.在育种群体中定位农艺性状的 QTL。
Theor Appl Genet. 2012 Jul;125(2):201-10. doi: 10.1007/s00122-012-1887-6. Epub 2012 May 22.
10
QTL detection power of multi-parental RIL populations in Arabidopsis thaliana.拟南芥多亲本 RIL 群体的 QTL 检测能力。
Heredity (Edinb). 2012 Jun;108(6):626-32. doi: 10.1038/hdy.2011.133. Epub 2012 Feb 15.