Joint analysis of days to flowering reveals independent temperate adaptations in maize.


Journal

Heredity
ISSN: 1365-2540
Titre abrégé: Heredity (Edinb)
Pays: England
ID NLM: 0373007

Informations de publication

Date de publication:
06 2021
Historique:
received: 20 02 2020
accepted: 25 02 2021
revised: 07 02 2021
pubmed: 24 4 2021
medline: 26 10 2021
entrez: 23 4 2021
Statut: ppublish

Résumé

Domesticates are an excellent model for understanding biological consequences of rapid climate change. Maize (Zea mays ssp. mays) was domesticated from a tropical grass yet is widespread across temperate regions today. We investigate the biological basis of temperate adaptation in diverse structured nested association mapping (NAM) populations from China, Europe (Dent and Flint) and the United States as well as in the Ames inbred diversity panel, using days to flowering as a proxy. Using cross-population prediction, where high prediction accuracy derives from overall genomic relatedness, shared genetic architecture, and sufficient diversity in the training population, we identify patterns in predictive ability across the five populations. To identify the source of temperate adapted alleles in these populations, we predict top associated genome-wide association study (GWAS) identified loci in a Random Forest Classifier using independent temperate-tropical North American populations based on lines selected from Hapmap3 as predictors. We find that North American populations are well predicted (AUC equals 0.89 and 0.85 for Ames and USNAM, respectively), European populations somewhat well predicted (AUC equals 0.59 and 0.67 for the Dent and Flint panels, respectively) and that the Chinese population is not predicted well at all (AUC is 0.47), suggesting an independent adaptation process for early flowering in China. Multiple adaptations for the complex trait days to flowering in maize provide hope for similar natural systems under climate change.

Identifiants

pubmed: 33888874
doi: 10.1038/s41437-021-00422-z
pii: 10.1038/s41437-021-00422-z
pmc: PMC8178344
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

929-941

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Auteurs

Kelly Swarts (K)

Gregor Mendel Institute, Austrian Academy of Sciences, Vienna Biocenter, Vienna, Austria. kelly.swarts@gmi.oeaw.ac.at.
Department of Structural and Computational Biology, Max F. Perutz Laboratories, University of Vienna, Vienna Biocenter, Vienna, Austria. kelly.swarts@gmi.oeaw.ac.at.
Department of Plant Breeding and Genetics, Cornell University, Ithaca, NY, USA. kelly.swarts@gmi.oeaw.ac.at.

Eva Bauer (E)

Plant Breeding, TUM School of Life Sciences Weihenstephan, Technical University of Munich, Freising, Germany.

Jeffrey C Glaubitz (JC)

Institute for Genomic Diversity, Institute of Biotechnology, Cornell University, Ithaca, NY, USA.

Tiffany Ho (T)

Department of Plant Breeding and Genetics, Cornell University, Ithaca, NY, USA.

Lynn Johnson (L)

Institute for Genomic Diversity, Institute of Biotechnology, Cornell University, Ithaca, NY, USA.

Yongxiang Li (Y)

Institute of Crop Science, Chinese Academy of Agricultural Sciences, Beijing, China.

Yu Li (Y)

Institute of Crop Science, Chinese Academy of Agricultural Sciences, Beijing, China.

Zachary Miller (Z)

Institute for Genomic Diversity, Institute of Biotechnology, Cornell University, Ithaca, NY, USA.

Cinta Romay (C)

Institute for Genomic Diversity, Institute of Biotechnology, Cornell University, Ithaca, NY, USA.

Chris-Carolin Schön (CC)

Plant Breeding, TUM School of Life Sciences Weihenstephan, Technical University of Munich, Freising, Germany.

Tianyu Wang (T)

Institute of Crop Science, Chinese Academy of Agricultural Sciences, Beijing, China.

Zhiwu Zhang (Z)

Department of Crop and Soil Sciences, Washington State University, Pullman, WA, USA.

Edward S Buckler (ES)

Department of Plant Breeding and Genetics, Cornell University, Ithaca, NY, USA.
USDA-ARS, Ithaca, NY, USA.

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