Improving protein quality and grain yield traits coordinately is an important goal for crop breeding. To date, many protein-quality or grain-yield regulation genes have been identified. However, the genetic strategies integrating these genes in good-protein-quality and high-yield crop breeding practice are far from established. Here, we characterized the functions of the MADS domain-containing protein ZmMADS8 and Zea mays G protein gamma subunit 1 (ZmGG1) in regulating protein quality and grain yield of maize. ZmMADS8 positively regulates zein protein accumulation and negatively regulates non-zein protein and lysine levels in kernels by interacting with ZmMADS47 to promote the transcriptional activation of Opaque2. Additionally, ZmMADS8 regulates starch content of kernels by targeting genes involved in starch biosynthesis. ZmGG1, a putative interactor of ZmMADS8, negatively regulates kernel number with a trade-off effect on kernel starch accumulation. The mads8;zmgg1 double mutant improved protein quality by attenuating zein biosynthesis and increasing essential lysine level, and increased grain yield by increasing kernel number, compensating for decreased starch biosynthesis. Our findings revealed the biological function of ZmMADS8 and ZmGG1 in regulating protein quality and yield related traits and suggested a genetic strategy by direct editing of ZmMADS8 and ZmGG1 to improve grain yield and protein quality simultaneously.
- Article type
- Year
- Co-author
Open Access
Research paper
Issue
Open Access
Research paper
Issue
Gray leaf spot (GLS) caused by Cercospora zeae-maydis and C. zeina is an extremely devastating leaf disease that limits maize production annually. The use of GLS-resistant maize hybrids is the most cost-effective approach for reducing losses. Resistance to GLS is quantitatively inherited in maize (Zea mays L.) and further sources of resistance remain to be analyzed. Here, we detected qRgls1.06, a major quantitative trait locus for GLS resistance in bin 1.06 that explained approximately 55% of the phenotype variance. Fine mapping over 2 consecutive years localized qRgls1.06 to a 2.38-Mb region. Homozygous qRgls1.06WGR/WGR plants in DZ01 background displayed higher GLS resistance and 100-grain weight than DZ01 plants. The GLS responses of several susceptible elite inbred lines were improved by the introduction of qRgls1.06 by marker-assisted backcrossing. Our findings extend the understanding of the genetic basis of resistance to GLS and provide a set of resistant germplasm for genetic improvement of resistance to GLS in maize.
京公网安备11010802044758号