芸苔属
加倍单倍体
回交
生物
细胞质雄性不育
倍性
突变体
异交
油菜
甘蓝
杂种优势
不育
生物技术
植物
遗传学
基因
花粉
混合的
作者
Fengqing Han,Xiaoli Zhang,Yuxiang Liu,Yumei Liu,Hong Zhao,Zhansheng Li
标识
DOI:10.1038/s41477-024-01643-w
摘要
Heterosis utilization in a large proportion of crops depends on the use of cytoplasmic male sterility (CMS) tools, requiring the development of homozygous fertile lines and CMS lines1. Although doubled haploid (DH) technology has been developed for several crops to rapidly generate fertile lines2,3, CMS lines are generally created by multiple rounds of backcrossing, which is time consuming and expensive4. Here we describe a method for generating both homozygous fertile and CMS lines through in vivo paternal haploid induction (HI). We generated in-frame deletion and restored frameshift mutants of BoCENH3 in Brassica oleracea using the CRISPR/Cas9 system. The mutants induced paternal haploids by outcrossing. We subsequently generated HI lines with CMS cytoplasm, which enabled the generation of homozygous CMS lines in one step. The BoCENH3-based HI system provides a new DH technology to accelerate breeding in Brassica and other crops.
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