z-logo
open-access-imgOpen Access
Genome-Wide Association and Regional Heritability Mapping of Plant Architecture, Lodging and Productivity inPhaseolus vulgaris
Author(s) -
Rafael Tassinari Resende,
Marcos Deon Vilela de Resende,
Camila Ferreira Azevedo,
Fabyano Fonseca e Silva,
L. C. Melo,
H. S. Pereira,
T. L. P. O. de Souza,
Paula Arielle Mendes Ribeiro Valdisser,
Cláudio Brondani,
Rosana Pereira Vianello
Publication year - 2018
Publication title -
g3 genes genomes genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.468
H-Index - 66
ISSN - 2160-1836
DOI - 10.1534/g3.118.200493
Subject(s) - heritability , genome wide association study , genetic architecture , quantitative trait locus , biology , genetics , genetic association , trait , genotyping , missing heritability problem , association mapping , germplasm , phaseolus , allele , genotype , gene , single nucleotide polymorphism , agronomy , computer science , programming language
The availability of high-density molecular markers in common bean has allowed to explore the genetic basis of important complex agronomic traits with increased resolution. Genome-Wide Association Studies (GWAS) and Regional Heritability Mapping (RHM) are two analytical approaches for the detection of genetic variants. We carried out GWAS and RHM for plant architecture, lodging and productivity across two important growing environments in Brazil in a germplasm of 188 common bean varieties using DArTseq genotyping strategies. The coefficient of determination of G × E interaction (c 2 int ) was equal to 17, 21 and 41%, respectively for the traits architecture, lodging, and productivity. Trait heritabilities were estimated at 0.81 (architecture), 0.79 (lodging) and 0.43 (productivity), and total genomic heritability accounted for large proportions (72% to ≈100%) of trait heritability. At the same probability threshold, three marker-trait associations were detected using GWAS, while RHM detected eight QTL encompassing 145 markers along five chromosomes. The proportion of genomic heritability explained by RHM was considerably higher (35.48 to 58.02) than that explained by GWAS (28.39 to 30.37). In general, RHM accounted for larger fractions of the additive genetic variance being captured by markers effects inside the defined regions. Nevertheless, a considerable proportion of the heritability is still missing (∼42% to ∼64%), probably due to LD between markers and genes and/or rare allele variants not sampled. RHM in autogamous species had the potential to identify larger-effect QTL combining allelic variants that could be effectively incorporated into whole-genome prediction models and tracked through breeding generations using marker-assisted selection.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom