A Class II KNOX Gene, KNAT7-1, Regulates Physical Seed Dormancy in Mungbean [Vigna radiata (L.) Wilczek]
Quantitative trait locus
0301 basic medicine
mungbean
Population
Germination
Plant Science
KNAT7
Gene
hardseededness
SB1-1110
Genetic Diversity and Improvement of Soybean
Agricultural and Biological Sciences
03 medical and health sciences
Sociology
Symbiotic Nitrogen Fixation in Legumes
Plant Signaling
Genetics
Radiata
Dormancy
Biology
Demography
2. Zero hunger
Vigna
seed dormancy
Botany
Plant culture
Life Sciences
Seed dormancy
KNOX II
15. Life on land
FOS: Sociology
FOS: Biological sciences
Locus (genetics)
Genetics and Breeding of Cowpea
DOI:
10.3389/fpls.2022.852373
Publication Date:
2022-03-15T09:39:38Z
AUTHORS (9)
ABSTRACT
Seed dormancy in wild mungbean (Vigna radiata var. sublobata) may be useful for the breeding of cultivated mungbean (var. radiata) with pre-harvest sprouting resistance. Previous studies have identified two major quantitative trait loci (QTLs) for seed dormancy, HsA and Sdwa5.1.1+, in wild mungbean that are possibly having the same locus or linked. However, these QTLs have not been confirmed/verified and a molecular basis of seed dormancy in mungbean is not yet known. In this study, we aimed to finely map the Sdwa5.1.1+ and identify candidate gene(s) for this locus. Microscopic observations revealed that wild mungbean “ACC41” seeds had a palisade cuticle layer, while cultivated mungbean “Kamphaeng Saen 2” (KPS2) seeds lacked this layer. Fine mapping using an F2 population developed from a cross between ACC41 and KPS2 revealed two linked QTLs, Sdwa5.1.1+ and Sdwa5.1.2+, controlling seed dormancy. The Sdwa5.1.1+ was confirmed in an F2:3 population derived from the same cross and mapped to a 3.298-Kb region containing only one gene LOC106767068, designated as VrKNAT7-1, which encodes the transcription factor KNOTTED ARABIDOPSIS THALIANA7 (KNAT7), a class II KNOTTED1-LIKE HOMEOBOX (KNOX II) protein. VrKNAX7 sequence alignment between ACC41 and KPS2 revealed several polymorphisms in the coding, untranslated, and promoter regions. Quantitative real-time PCR (qRT-PCR) analysis revealed that the expression of VrKNAT7-1 and VrCYP86A, a putative downstream regulation of VrKNAT7-1, in the seed coat of ACC41 is statistically much higher than that of KPS2. Altogether, these results indicate that VrKNAT7-1 controls physical seed dormancy in the wild mungbean ACC41.
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