Long-read sequencing reveals genomic structural variations that underlie creation of quality protein maize
Changsheng Li, Xiaoli Xiang, Yongcai Huang, Yong Zhou, Dong An, Jiaqiang Dong, Chenxi Zhao, Hongjun Liu, Yubin Li, Qiong Wang, Chunguang Du, Joachim Messing, Brian A. Larkins, Yongrui Wu, Wenqin Wang
Abstract
Abstract Mutation of o2 doubles maize endosperm lysine content, but it causes an inferior kernel phenotype. Developing quality protein maize (QPM) by introgressing o2 modifier s ( Mo2 s) into the o2 mutant benefits millions of people in developing countries where maize is a primary protein source. Here, we report genome sequence and annotation of a South African QPM line K0326Y, which is assembled from single-molecule, real-time shotgun sequencing reads collinear with an optical map. We achieve a N50 contig length of 7.7 million bases (Mb) directly from long-read assembly, compared to those of 1.04 Mb for B73 and 1.48 Mb for Mo17. To characterize Mo2 s, we map QTLs to chromosomes 1, 6, 7, and 9 using an F 2 population derived from crossing K0326Y and W64A o2 . RNA-seq analysis of QPM and o2 endosperms reveals a group of differentially expressed genes that coincide with Mo2 QTLs, suggesting a potential role in vitreous endosperm formation.