Affiliation:
1. Henan Academy of Agricultural Sciences
2. Chinese Academy of Agricultural Sciences
3. Institute of Genetics and Developmental Biology CAS: Institute of Genetics and Developmental Biology Chinese Academy of Sciences
4. Institute of Wheat, Henan Academy of Agricultural Sciences
Abstract
AbstractEffective tillers contribute to yield through adjusting population structure and affect 1000-kernel weight and kernel number per spike, which are favorable for wheat (Triticum aestivum) improvement. Wheat landraces show strong tillering ability and thus considerable potential for utilization in breeding. In this study, tiller number under nutrient solution condition was evaluated for 269 wheat recombinant inbred lines and their parents: the modern cultivar Beinong 6 and the landrace Yanda 1817, which exhibit strong tillering ability. A stable QTL,qTN-7B.1, significant in three independent experiments, was mapped between genetic markerXgwm333and7ABD_wsnp_be518436B_Ta_2_1. The positive allele ofqTN-7B.1was from Yanda 1817, explained 10.21%-18.89% phenotypic variations. Pathway enrichment among tiller-bud transcriptome data for the two parents suggested that tillering ability was mainly associated with lignin biosynthesis and energy metabolism. Comparative genomic indicated that wheat homologous geneTaMoc1-7Bwas located inqTN-7B.1but was excluded for candidate since no high-impact sequence variations between parents and no transcript abundance during tiller bud development. Compared with published QTL for tiller suggested thatqTN-7B.1was most likely the novel. Further analysis the differentially gene expression analysis and variant through transcriptome data identified 33 nonsynonymous SNVs on 20 DEGs. In particular,TraesCS7B02G282100encoded cinnamyl alcohol dehydrogenase crucially in lignin biosynthesis that the expression level of Beinong 6 exhibited 3.179-fold up-regulated and a synonymous SNP at conserved domain between parents, Therefore,TraesCS7B02G282100was considered as candidate gene. Based on this SNP, a KASP marker was developed that anchored withinqTN-7B.1genetic region. This study laid the foundation for map-based cloning ofqTN-7B.1and provided genetic marker for plant architecture improvement through molecular breeding.
Publisher
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