QTL MAPPING REVEALS A STRIKING COINCIDENCE IN THE POSITIONS OF GENOMIC REGIONS ASSOCIATED WITH ADAPTIVE VARIATION IN BODY SIZE IN PARALLEL CLINES OF DROSOPHILA MELANOGASTER ON DIFFERENT CONTINENTS

• Published in: Evolution 2003-11, Vol.57 (11), p.2653-2658
• Main Authors: Calboli, Federico C. F, Kennington, W. Jason, Partridge, Linda
• Format: Article
• Language: English
• Subjects: Adaptation, Biological; Animals; Australia; Body size; Body Weights and Measures; BRIEF COMMUNICATIONS; Chromosome Inversion; Chromosomes; Drosophila; Drosophila melanogaster - genetics; Evolutionary genetics; genetic differentiation; Genetic Markers; Genetic variation; Geography; latitudinal cline; Likelihood Functions; Lod score; natural selection; Phenotypic traits; Quantitative genetics; Quantitative trait loci; Quantitative Trait Loci - genetics; Selection, Genetic; South America; Thorax; Wings, Animal - anatomy & histology
• ISSN: 0014-3820; 1558-5646
• DOI: 10.1554/03-167

Latitudinal genetic clines in body size are common in many ectotherm species and are attributed to climatic adaptation. Here, we use Quantitative Trait Loci (QTL) mapping to identify genomic regions associated with adaptive variation in body size in natural populations of Drosophila melanogaster from extreme ends of a cline in South America. Our results show that there is a significant association between the positions of QTL with strong effects on wing area in South America and those previously reported in a QTL mapping study of Australian cline end populations (P < 0.05). In both continents, the right arm of the third chromosome is associated with QTL with the strongest effect on wing area. We also show that QTL peaks for wing area and thorax length are associated with the same genomic regions, indicating that the clinal variation in the body size traits may have a similar genetic basis. The consistency of the results found for the South American and Australian cline end populations indicate that the genetic basis of the two clines may be similar and future efforts to identify the genes producing the response to selection should be focused on the genomic regions highlighted by the present work.