Combining QTL-seq and linkage mapping to uncover the genetic basis of single vs. paired spikelets in the advanced populations of two-ranked maize×teosinte

数量性状位点 生物 上位性 基于家系的QTL定位 遗传学 基因座(遗传学) 包含复合区间映射 基因定位 基因 染色体
作者
Zhengjie Chen,Dengguo Tang,Kun Hu,Lei Zhang,Yong Yin,Jixing Ni,Peng Li,Le Wang,Tingzhao Rong,Jian Liu
出处
期刊:BMC Plant Biology [BioMed Central]
卷期号:21 (1) 被引量:5
标识
DOI:10.1186/s12870-021-03353-3
摘要

Abstract Background Teosinte ear bears single spikelet, whereas maize ear bears paired spikelets, doubling the number of grains in each cupulate during maize domestication. In the past 20 years, genetic analysis of single vs. paired spikelets (PEDS) has been stagnant. A better understanding of genetic basis of PEDS could help fine mapping of quantitative trait loci (QTL) and cloning of genes. Results In this study, the advanced mapping populations (BC 3 F 2 and BC 4 F 2 ) of maize × teosinte were developed by phenotypic recurrent selection. Four genomic regions associated with PEDS were detected using QTL-seq, located on 194.64–299.52 Mb, 0–162.80 Mb, 12.82–97.17 Mb, and 125.06–157.01 Mb of chromosomes 1, 3, 6, and 8, respectively. Five QTL for PEDS were identified in the regions of QTL-seq using traditional QTL mapping. Each QTL explained 1.12–38.05% of the phenotypic variance (PVE); notably, QTL qPEDS3.1 with the average PVE of 35.29% was identified in all tests. Moreover, 14 epistatic QTL were detected, with the total PVE of 47.57–66.81% in each test. The QTL qPEDS3.1 overlapped with, or was close to, one locus of 7 epistatic QTL. Near-isogenic lines (NILs) of QTL qPEDS1.1 , qPEDS3.1 , qPEDS6.1 , and qPEDS8.1 were constructed. All individuals of NIL- qPEDS6.1 (MT1) and NIL- qPEDS8.1 (MT1) showed paired spikelets (PEDS = 0), but the flowering time was 7 days shorter in the NIL- qPEDS8.1 (MT1). The ratio of plants with PEDS > 0 was low (1/18 to 3/18) in the NIL- qPEDS1.1 (MT1) and NIL- qPEDS3.1 (MT1), maybe due to the epistatic effect. Conclusion Our results suggested that major QTL, minor QTL, epistasis and photoperiod were associated with the variation of PEDS, which help us better understand the genetic basis of PEDS and provide a genetic resource for fine mapping of QTL.

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