Rapid identification of a major locus qPRL-C06 affecting primary root length in Brassica napus by QTL-seq

Author:

Wang Wei12,Liu Haijiang12,Xie Yiwen12,King Graham John3,White Philip John14,Zou Jun1,Xu Fangsen12ORCID,Shi Lei12ORCID

Affiliation:

1. National Key Laboratory of Crop Genetic Improvement, Huazhong Agricultural University , Wuhan 430070 , China

2. Microelement Research Center, Key Laboratory of Arable Land Conservation (Middle and Lower Reaches of Yangtze River), Ministry of Agriculture and Rural Affairs, Huazhong Agricultural University , Wuhan 430070 , China

3. Southern Cross Plant Science, Southern Cross University , Lismore NSW 2480 , Australia

4. The James Hutton Institute, Invergowrie , Dundee DD2 5DA , UK

Abstract

Abstract Background and Aims Brassica napus is one of the most important oilseed crops worldwide. Seed yield of B. napus significantly correlates with the primary root length (PRL). The aims of this study were to identify quantitative trait loci (QTLs) for PRL in B. napus. Methods QTL-seq and conventional QTL mapping were jointly used to detect QTLs associated with PRL in a B. napus double haploid (DH) population derived from a cross between ‘Tapidor’ and ‘Ningyou 7’. The identified major locus was confirmed and resolved by an association panel of B. napus and an advanced backcross population. RNA-seq analysis of two long-PRL lines (Tapidor and TN20) and two short-PRL lines (Ningyou 7 and TN77) was performed to identify differentially expressed genes in the primary root underlying the target QTLs. Key Results A total of 20 QTLs impacting PRL in B. napus grown at a low phosphorus (P) supply were found by QTL-seq. Eight out of ten QTLs affecting PRL at a low P supply discovered by conventional QTL mapping could be detected by QTL-seq. The locus qPRL-C06 identified by QTL-seq was repeatedly detected at both an optimal P supply and a low P supply by conventional QTL mapping. This major constitutive QTL was further confirmed by regional association mapping. qPRL-C06 was delimited to a 0.77 Mb genomic region on chromosome C06 using an advanced backcross population. A total of 36 candidate genes within qPRL-C06 were identified that showed variations in coding sequences and/or exhibited significant differences in mRNA abundances in primary root between the long-PRL and short-PRL lines, including five genes involved in phytohormone biosynthesis and signaling. Conclusions These results both demonstrate the power of the QTL-seq in rapid QTL detection for root traits and will contribute to marker-assisted selective breeding of B. napus cultivars with increased PRL.

Funder

National Nature Science Foundation of China

Natural and Fundamental Research Funds for the Central Universities of China

Publisher

Oxford University Press (OUP)

Subject

Plant Science

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