Literature DB >> 16538513

Mapping QTLs and QTL x environment interaction for CIMMYT maize drought stress program using factorial regression and partial least squares methods.

Mateo Vargas1, Fred A van Eeuwijk, Jose Crossa, Jean-Marcel Ribaut.   

Abstract

The study of QTL x environment interaction (QEI) is important for understanding genotype x environment interaction (GEI) in many quantitative traits. For modeling GEI and QEI, factorial regression (FR) models form a powerful class of models. In FR models, covariables (contrasts) defined on the levels of the genotypic and/or environmental factor(s) are used to describe main effects and interactions. In FR models for QTL expression, considerable numbers of genotypic covariables can occur as for each putative QTL an additional covariable needs to be introduced. For large numbers of genotypic and/or environmental covariables, least square estimation breaks down and partial least squares (PLS) estimation procedures become an attractive alternative. In this paper we develop methodology for analyzing QEI by FR for estimating effects and locations of QTLs and QEI and interpreting QEI in terms of environmental variables. A randomization test for the main effects of QTLs and QEI is presented. A population of F2 derived F3 families was evaluated in eight environments differing in drought stress and soil nitrogen content and the traits yield and anthesis silking interval (ASI) were measured. For grain yield, chromosomes 1 and 10 showed significant QEI, whereas in chromosomes 3 and 8 only main effect QTLs were observed. For ASI, QTL main effects were observed on chromosomes 1, 2, 6, 8, and 10, whereas QEI was observed only on chromosome 8. The assessment of the QEI at chromosome 1 for grain yield showed that the QTL main effect explained 35.8% of the QTL + QEI variability, while QEI explained 64.2%. Minimum temperature during flowering time explained 77.6% of the QEI. The QEI analysis at chromosome 10 showed that the QTL main effect explained 59.8% of the QTL + QEI variability, while QEI explained 40.2%. Maximum temperature during flowering time explained 23.8% of the QEI. Results of this study show the possibilities of using FR for mapping QTL and for dissecting QEI in terms of environmental variables. PLS regression is efficient in accounting for background noise produced by other QTLs.

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Year:  2006        PMID: 16538513     DOI: 10.1007/s00122-005-0204-z

Source DB:  PubMed          Journal:  Theor Appl Genet        ISSN: 0040-5752            Impact factor:   5.699


  12 in total

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Authors:  C A Hackett; R C Meyer; W T Thomas
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3.  Interpreting genotype × environment interaction in tropical maize using linked molecular markers and environmental covariables.

Authors:  J Crossa; M Vargas; F A van Eeuwijk; C Jiang; G O Edmeades; D Hoisington
Journal:  Theor Appl Genet       Date:  1999-08       Impact factor: 5.699

4.  A simple regression method for mapping quantitative trait loci in line crosses using flanking markers.

Authors:  C S Haley; S A Knott
Journal:  Heredity (Edinb)       Date:  1992-10       Impact factor: 3.821

5.  Identification of quantitative trait loci under drought conditions in tropical maize. 1. Flowering parameters and the anthesis-silking interval.

Authors:  J M Ribaut; D A Hoisington; J A Deutsch; C Jiang; D Gonzalez-de-Leon
Journal:  Theor Appl Genet       Date:  1996-05       Impact factor: 5.699

6.  Estimating the locations and the sizes of the effects of quantitative trait loci using flanking markers.

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7.  Mapping quantitative trait loci with dominant and missing markers in various crosses from two inbred lines.

Authors:  C Jiang; Z B Zeng
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8.  Mapping mendelian factors underlying quantitative traits using RFLP linkage maps.

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Authors:  Z B Zeng
Journal:  Genetics       Date:  1994-04       Impact factor: 4.562

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Authors:  A Bjørnstad; S Grønnerød; J Mac Key; A Tekauz; J Crossa; H Martens
Journal:  Hereditas       Date:  2004       Impact factor: 3.271

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  29 in total

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Journal:  Theor Appl Genet       Date:  2012-05       Impact factor: 5.699

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3.  Using probe genotypes to dissect QTL × environment interactions for grain yield components in winter wheat.

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Journal:  Theor Appl Genet       Date:  2010-08-10       Impact factor: 5.699

4.  Genome-Wide Analysis of Yield in Europe: Allelic Effects Vary with Drought and Heat Scenarios.

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Journal:  Plant Physiol       Date:  2016-07-19       Impact factor: 8.340

5.  Precise mapping of quantitative trait loci for resistance to southern leaf blight, caused by Cochliobolus heterostrophus race O, and flowering time using advanced intercross maize lines.

Authors:  P J Balint-Kurti; J C Zwonitzer; R J Wisser; M L Carson; M A Oropeza-Rosas; J B Holland; S J Szalma
Journal:  Genetics       Date:  2007-03-04       Impact factor: 4.562

6.  Quantitative trait loci and crop performance under abiotic stress: where do we stand?

Authors:  Nicholas C Collins; François Tardieu; Roberto Tuberosa
Journal:  Plant Physiol       Date:  2008-06       Impact factor: 8.340

7.  Addressing drought tolerance in maize by transcriptional profiling and mapping.

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8.  Multi-trait and multi-environment QTL analyses of yield and a set of physiological traits in pepper.

Authors:  N A Alimi; M C A M Bink; J A Dieleman; J J Magán; A M Wubs; A Palloix; F A van Eeuwijk
Journal:  Theor Appl Genet       Date:  2013-08-01       Impact factor: 5.699

9.  Simulating the yield impacts of organ-level quantitative trait loci associated with drought response in maize: a "gene-to-phenotype" modeling approach.

Authors:  Karine Chenu; Scott C Chapman; François Tardieu; Greg McLean; Claude Welcker; Graeme L Hammer
Journal:  Genetics       Date:  2009-09-28       Impact factor: 4.562

10.  QTL analysis for yield components and kernel-related traits in maize across multi-environments.

Authors:  Bo Peng; Yongxiang Li; Yang Wang; Cheng Liu; Zhizhai Liu; Weiwei Tan; Yan Zhang; Di Wang; Yunsu Shi; Baocheng Sun; Yanchun Song; Tianyu Wang; Yu Li
Journal:  Theor Appl Genet       Date:  2011-02-01       Impact factor: 5.699

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