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Genome-Edited Triple-Recessive Mutation Alters Seed Dormancy in Wheat

Authors :
Kanako Kawaura
Takeshi Hayashi
Kazumitsu Onishi
Kazuhiro Sato
Hiroshi Hisano
Fumitaka Abe
Masafumi Mikami
Masaki Endo
Yoko Kamiya
Tsuyoshi Tanaka
Emdadul Haque
Source :
SC30202004010017, NARO成果DBa, 表示-非営利-改変禁止(CC-BY-NC-ND), C30202003140001_9493, Cell Reports, Vol 28, Iss 5, Pp 1362-1369.e4 (2019)
Publication Year :
2018

Abstract

Summary: Common wheat has three sets of sub-genomes, making mutations difficult to observe, especially for traits controlled by recessive genes. Here, we produced hexaploid wheat lines with loss of function of homeoalleles of Qsd1, which controls seed dormancy in barley, by Agrobacterium-mediated CRISPR/Cas9. Of the eight transformed wheat events produced, three independent events carrying multiple mutations in wheat Qsd1 homeoalleles were obtained. Notably, one line had mutations in every homeoallele. We crossed this plant with wild-type cultivar Fielder to generate a transgene-free triple-recessive mutant, as revealed by Mendelian segregation. The mutant showed a significantly longer seed dormancy period than wild-type, which may result in reduced pre-harvest sprouting of grains on spikes. PCR, southern blotting, and whole-genome shotgun sequencing revealed that this segregant lacked transgenes in its genomic sequence. This technique serves as a model for trait improvement in wheat, particularly for genetically recessive traits, based on locus information from diploid barley. : Using Agrobacterium-delivered CRISPR/Cas9, Abe et al. developed a loss-of-function triple mutation of Qsd1, which controls seed dormancy in barley, resulting in longer seed dormancy in wheat. This serves as a model technique for the improvement of wheat traits, particularly genetically recessive traits, based on locus information for diploid barley. Keywords: wheat, Qsd1, seed dormancy, CRISPR/Cas9, multiple mutation

Details

ISSN :
22111247
Volume :
28
Issue :
5
Database :
OpenAIRE
Journal :
Cell reports
Accession number :
edsair.doi.dedup.....26b2eca5833c7e7d8f0d2c1085f1b46a
Full Text :
https://doi.org/10.1016/j.celrep.2019.06.090