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De novo genome assembly and analyses of 12 founder inbred lines provide insights into maize heterosis.

Baobao WangMei HouJunpeng ShiLixia KuWei SongChunhui LiQiang NingXin LiChangyu LiBinbin ZhaoRuyang ZhangHua XuZhijing BaiZhanchao XiaHai WangDexin KongHongbin WeiYifeng JingZhouyan DaiHu Hailing WangXinyu ZhuChunhui LiXuan SunShuaishuai WangWen YaoGege HouZhi QiHe DaiXuming LiHongkun ZhengZhuxin ZhangYu LiTianyu WangTaijiao JiangZhaoman WanYanhui ChenJiuran ZhaoJinsheng LaiHai-Yang Wang
Published in: Nature genetics (2023)
Hybrid maize displays superior heterosis and contributes over 30% of total worldwide cereal production. However, the molecular mechanisms of heterosis remain obscure. Here we show that structural variants (SVs) between the parental lines have a predominant role underpinning maize heterosis. De novo assembly and analyses of 12 maize founder inbred lines (FILs) reveal abundant genetic variations among these FILs and, through expression quantitative trait loci and association analyses, we identify several SVs contributing to genomic and phenotypic differentiations of various heterotic groups. Using a set of 91 diallel-cross F 1 hybrids, we found strong positive correlations between better-parent heterosis of the F 1 hybrids and the numbers of SVs between the parental lines, providing concrete genomic support for a prevalent role of genetic complementation underlying heterosis. Further, we document evidence that SVs in both ZAR1 and ZmACO2 contribute to yield heterosis in an overdominance fashion. Our results should promote genomics-based breeding of hybrid maize.
Keyphrases
  • genome wide
  • copy number
  • dna methylation
  • poor prognosis
  • single cell
  • gene expression