Suppr超能文献

全基因组关联分析鉴定决定小麦早熟性构成的染色体区域。

Genome-wide association analysis to identify chromosomal regions determining components of earliness in wheat.

机构信息

INRA, UMR 1095 Génétique, Diversité et Ecophysiologie des Céréales, 234 Avenue du Brézet, 63 100, Clermont-Ferrand, France.

出版信息

Theor Appl Genet. 2012 Feb;124(3):597-611. doi: 10.1007/s00122-011-1732-3. Epub 2011 Nov 8.

Abstract

The modification of flowering date is considered an important way to escape the current or future climatic constraints that affect wheat crops. A better understanding of its genetic bases would enable a more efficient and rapid modification through breeding. The objective of this study was to identify chromosomal regions associated with earliness in wheat. A 227-wheat core collection chosen to be highly contrasted for earliness was characterized for heading date. Experiments were conducted in controlled conditions and in the field for 3 years to break down earliness in the component traits: photoperiod sensitivity, vernalization requirement and narrow-sense earliness. Whole-genome association mapping was carried out using 760 molecular markers and taking into account the five ancestral group structure. We identified 62 markers individually associated to earliness components corresponding to 33 chromosomal regions. In addition, we identified 15 other significant markers and seven more regions by testing marker pair interactions. Co-localizations were observed with the Ppd-1, Vrn-1 and Rht-1 candidate genes. Using an independent set of lines to validate the model built for heading date, we were able to explain 34% of the variation using the structure and the significant markers. Results were compared with already published data using bi-parental populations giving an insight into the genetic architecture of flowering time in wheat.

摘要

改变开花日期被认为是逃避当前或未来影响小麦作物的气候限制的重要方法。更好地了解其遗传基础将使通过育种进行更高效和快速的修饰成为可能。本研究的目的是鉴定与小麦早熟性相关的染色体区域。选择了一个 227 个小麦核心群体,该群体选择高度对比早熟性,用于测定抽穗期。在控制条件和田间进行了 3 年的实验,以分解组成性状的早熟性:光周期敏感性、春化要求和狭义早熟性。使用 760 个分子标记并考虑到五个祖先群体结构进行了全基因组关联作图。我们鉴定了 62 个与早熟性成分单独相关的标记,对应于 33 个染色体区域。此外,通过测试标记对相互作用,我们还鉴定了 15 个其他显著标记和 7 个更多的区域。与 Ppd-1、Vrn-1 和 Rht-1 候选基因观察到共定位。使用一组独立的系来验证为抽穗期构建的模型,我们能够使用结构和显著标记解释 34%的变异。将结果与使用双亲群体已经发表的数据进行比较,深入了解小麦开花时间的遗传结构。

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