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将数量性状基因座定位到亚麻的染色体级假分子上。

Mapping Quantitative Trait Loci onto Chromosome-Scale Pseudomolecules in Flax.

作者信息

You Frank M, Cloutier Sylvie

机构信息

Ottawa Research and Development Centre, Agriculture and Agri-Food Canada, Ottawa, ON K1A 0C6, Canada.

出版信息

Methods Protoc. 2020 Apr 4;3(2):28. doi: 10.3390/mps3020028.

Abstract

Quantitative trait loci (QTL) are genomic regions associated with phenotype variation of quantitative traits. To date, a total of 313 QTL for 31 quantitative traits have been reported in 14 studies on flax. Of these, 200 QTL from 12 studies were identified based on genetic maps, the scaffold sequences, or the pre-released chromosome-scale pseudomolecules. Molecular markers for QTL identification differed across studies but the most used ones were simple sequence repeats (SSRs) or single nucleotide polymorphisms (SNPs). To uniquely map the SSR and SNP markers from different references onto the recently released chromosome-scale pseudomolecules, methods with several scripts and database files were developed to locate PCR- and SNP-based markers onto the same reference, co-locate QTL, and scan genome-wide candidate genes. Using these methods, 195 out of 200 QTL were successfully sorted onto the 15 flax chromosomes and grouped into 133 co-located QTL clusters; the candidate genes that co-located with these QTL clusters were also predicted. The methods and tools presented in this article facilitate marker re-mapping to a new reference, genome-wide QTL analysis, candidate gene scanning, and breeding applications in flax and other crops.

摘要

数量性状基因座(QTL)是与数量性状表型变异相关的基因组区域。迄今为止,在14项亚麻研究中已报道了31个数量性状的总共313个QTL。其中,来自12项研究的200个QTL是基于遗传图谱、支架序列或预先发布的染色体水平假分子鉴定出来的。不同研究中用于QTL鉴定的分子标记有所不同,但最常用的是简单序列重复(SSR)或单核苷酸多态性(SNP)。为了将来自不同参考文献的SSR和SNP标记唯一地映射到最近发布的染色体水平假分子上,开发了具有多个脚本和数据库文件的方法,以便将基于PCR和SNP的标记定位到同一参考文献上、使QTL共定位并扫描全基因组候选基因。使用这些方法,200个QTL中的195个成功地定位到了15条亚麻染色体上,并被分组为133个共定位的QTL簇;还预测了与这些QTL簇共定位的候选基因。本文介绍的方法和工具有助于将标记重新映射到新的参考文献上、进行全基因组QTL分析、扫描候选基因以及在亚麻和其他作物中的育种应用。

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