Genetics, Vol. 165, 353-365, September 2003, Copyright © 2003

Genotype-Environment Interactions at Quantitative Trait Loci Affecting Inflorescence Development in Arabidopsis thaliana

Mark C. Ungerera, Solveig S. Halldorsdottira, Michael D. Purugganana, and Trudy F. C. Mackaya
a Department of Genetics, North Carolina State University, Raleigh, North Carolina 27695

Corresponding author: Mark C. Ungerer, Box 7614, North Carolina State University, Raleigh, NC 27695., mcungere{at}unity.ncsu.edu (E-mail)

Communicating editor: O. SAVOLAINEN

Phenotypic plasticity and genotype-environment interactions (GEI) play a prominent role in plant morphological diversity and in the potential functional capacities of plant life-history traits. The genetic basis of plasticity and GEI, however, is poorly understood in most organisms. In this report, inflorescence development patterns in Arabidopsis thaliana were examined under different, ecologically relevant photoperiod environments for two recombinant inbred mapping populations (Ler x Col and Cvi x Ler) using a combination of quantitative genetics and quantitative trait locus (QTL) mapping. Plasticity and GEI were regularly observed for the majority of 13 inflorescence traits. These observations can be attributable (at least partly) to variable effects of specific QTL. Pooled across traits, 12/44 (27.3%) and 32/62 (51.6%) of QTL exhibited significant QTL x environment interactions in the Ler x Col and Cvi x Ler lines, respectively. These interactions were attributable to changes in magnitude of effect of QTL more often than to changes in rank order (sign) of effect. Multiple QTL x environment interactions (in Cvi x Ler) clustered in two genomic regions on chromosomes 1 and 5, indicating a disproportionate contribution of these regions to the phenotypic patterns observed. High-resolution mapping will be necessary to distinguish between the alternative explanations of pleiotropy and tight linkage among multiple genes.





This article has been cited by other articles:


Home page
GeneticsHome page
D. Sambandan, M. A. Carbone, R. R. H. Anholt, and T. F. C. Mackay
Phenotypic Plasticity and Genotype by Environment Interaction for Olfactory Behavior in Drosophila melanogaster
Genetics, June 1, 2008; 179(2): 1079 - 1088.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
C.-X. Ma, Q. Yu, A. Berg, D. Drost, E. Novaes, G. Fu, J. S. Yap, A. Tan, M. Kirst, Y. Cui, et al.
A Statistical Model for Testing the Pleiotropic Control of Phenotypic Plasticity for a Count Trait
Genetics, May 1, 2008; 179(1): 627 - 636.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
M. Imtiaz, F. C. Ogbonnaya, J. Oman, and M. van Ginkel
Characterization of Quantitative Trait Loci Controlling Genetic Variation for Preharvest Sprouting in Synthetic Backcross-Derived Wheat Lines
Genetics, March 1, 2008; 178(3): 1725 - 1736.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
M. C. Hall, I. Dworkin, M. C. Ungerer, and M. Purugganan
Genetics of microenvironmental canalization in Arabidopsis thaliana
PNAS, August 21, 2007; 104(34): 13717 - 13722.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
I. M. Ehrenreich, P. A. Stafford, and M. D. Purugganan
The Genetic Architecture of Shoot Branching in Arabidopsis thaliana: A Comparative Assessment of Candidate Gene Associations vs. Quantitative Trait Locus Mapping
Genetics, June 1, 2007; 176(2): 1223 - 1236.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
D.-L. Yang, R.-L. Jing, X.-P. Chang, and W. Li
Identification of Quantitative Trait loci and Environmental Interactions for Accumulation and Remobilization of Water-Soluble Carbohydrates in Wheat (Triticum aestivum L.) Stems
Genetics, May 1, 2007; 176(1): 571 - 584.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
J. J. B. Keurentjes, L. Bentsink, C. Alonso-Blanco, C. J. Hanhart, H. Blankestijn-De Vries, S. Effgen, D. Vreugdenhil, and M. Koornneef
Development of a Near-Isogenic Line Population of Arabidopsis thaliana and Comparison of Mapping Power With a Recombinant Inbred Line Population
Genetics, February 1, 2007; 175(2): 891 - 905.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
L. U. Gilliland, M. Magallanes-Lundback, C. Hemming, A. Supplee, M. Koornneef, L. Bentsink, and D. DellaPenna
Colloquium Paper: Genetic basis for natural variation in seed vitamin E levels in Arabidopsis thaliana
PNAS, December 5, 2006; 103(49): 18834 - 18841.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
W. Valdar, L. C. Solberg, D. Gauguier, W. O. Cookson, J. N. P. Rawlins, R. Mott, and J. Flint
Genetic and Environmental Effects on Complex Traits in Mice
Genetics, October 1, 2006; 174(2): 959 - 984.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Bot.Home page
I. M. Ehrenreich and M. D. Purugganan
The molecular genetic basis of plant adaptation
Am. J. Botany, July 1, 2006; 93(7): 953 - 962.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
A. T. W. Kraakman, R. E. Niks, P. M. M. M. Van den Berg, P. Stam, and F. A. Van Eeuwijk
Linkage Disequilibrium Mapping of Yield and Yield Stability in Modern Spring Barley Cultivars
Genetics, September 1, 2004; 168(1): 435 - 446.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
K. M. Olsen, S. S. Halldorsdottir, J. R. Stinchcombe, C. Weinig, J. Schmitt, and M. D. Purugganan
Linkage Disequilibrium Mapping of Arabidopsis CRY2 Flowering Time Alleles
Genetics, July 1, 2004; 167(3): 1361 - 1369.
[Abstract] [Full Text] [PDF]