Nested association mapping reveals the genetic architecture of spice emergence and anthesis timing in intermediate wheatgrass

被引:9
作者
Altendorf, Kayla R. [1 ]
Larson, Steven R. [2 ]
DeHaan, Lee R. [3 ]
Crain, Jared [4 ]
Neyhart, Jeff [5 ]
Dorn, Kevin M. [6 ]
Anderson, James A. [7 ]
机构
[1] USDA ARS, Irrigated Agr Res & Extens Ctr, Forage Seed & Cereal Res Unit, Prosser, WA 99350 USA
[2] Land Inst, Salina, KS 67401 USA
[3] Utah State Univ, Forage Range & Res Lab, USDA ARS, Logan, UT 84322 USA
[4] Kansas State Univ, Dept Plant Pathol, Manhattan, KS 66506 USA
[5] Univ Minnesota, GEMS Informat Initiat, St Paul, MN 55108 USA
[6] USDA ARS, Soil Management & Sugarbeet Res, Ft Collins, CO 80526 USA
[7] Univ Minnesota, Dept Agron & Plant Genet, St Paul, MN 55108 USA
关键词
Nested association mapping; intermediate wheatgrass; flowering time; FUSARIUM HEAD BLIGHT; VARIANT CALL FORMAT; PERENNIAL GRAIN; GROWTH-STAGES; DECIMAL CODE; BARLEY; RESISTANCE; PHOTOPERIOD; POPULATION; GENERATION;
D O I
10.1093/g3journal/jkab025
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Intermediate wheatgrass (Thinopyrum intermedium) is an outcrossing, cool season grass species currently undergoing direct domestication as a perennial grain crop. Though many traits are selection targets, understanding the genetic architecture of those important for local adaptation may accelerate the domestication process. Nested association mapping (NAM) has proven useful in dissecting the genetic control of agronomic traits many crop species, but its utility in primarily outcrossing, perennial species has yet to be demonstrated. Here, we introduce an intermediate wheatgrass NAM population developed by crossing ten phenotypically divergent donor parents to an adapted common parent in a reciprocal manner, yielding 1,168 F-1 progeny from 10 families. Using genotyping by sequencing, we identified 8,003 SNP markers and developed a population-specific consensus genetic map with 3,144 markers across 21 linkage groups. Using both genomewide association mapping and linkage mapping combined across and within families, we characterized the genetic control of flowering time. In the analysis of two measures of maturity across four separate environments, we detected as many as 75 significant QTL, many of which correspond to the same regions in both analysis methods across 11 chromosomes. The results demonstrate a complex genetic control that is variable across years, locations, traits, and within families. The methods were effective at detecting previously identified QTL, as well as new QTL that align closely to the well-characterized flowering time orthologs from barley, including Ppd-H1 and Constans. Our results demonstrate the utility of the NAM population for understanding the genetic control of flowering time and its potential for application to other traits of interest.
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页数:14
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