Genetic exchange versus genetic differentiation in a medium-sized inversion of Drosophila: the A2/AST arrangements of Drosophila subobscura

• Autor(a) principal: Nóbrega, Clévio
• Data de Publicação: 2008
• Outros Autores: Khadem, Mahnaz, Aguade, Montserrat, Segarra, Carmen
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
• Texto Completo: http://hdl.handle.net/10400.13/3712
• topic: Inversion polymorphism; Drosophila subobscura; Nucleotide polymorphism; Genetic differentiation; Genetic exchange; A2/Ast arrangements; .; Faculdade de Ciências da Vida

Chromosomal inversion polymorphism affects nucleotide variation at loci associated with inversions. In Drosophila subobscura, a species with a rich chromosomal inversion polymorphism and the largest recombinational map so far reported in the Drosophila genus, extensive genetic structure of nucleotide variation was detected in the segment affected by the O3 inversion, a moderately sized inversion at Muller’s element E. Indeed, a strong genetic differentiation all over O3 and no evidence of a higher genetic exchange in the center of the inversion than at breakpoints were detected. In order to ascertain, whether other polymorphic and differently sized inversions of D. subobscura also exhibited a strong genetic structure, nucleotide variation in 5 gene regions (P236, P275, P150, Sxl, and P125) located along the A2 inversion was analyzed in Ast and A2 chromosomes of D. subobscura. A2 is a medium-sized inversion at Muller’s element A and forms a single inversion loop in heterokaryotypes. The lower level of variation in A2 relative to Ast and the significant excess of low-frequency variants at polymorphic sites indicate that nucleotide variation at A2 is not at mutation–drift equilibrium. The closest region to an inversion breakpoint, P236, exhibits the highest level of genetic differentiation (FST) and of linkage disequilibrium (LD) between arrangements and variants at nucleotide polymorphic sites. The remaining 4 regions show a higher level of genetic exchange between A2 and Ast chromosomes than P236, as revealed by FST and LD estimates. However, significant genetic differentiation between the Ast and A2 arrangements was detected not only at P236 but also in the other 4 regions separated from the nearest breakpoint by 1.2–2.9 Mb. Therefore, the extent of genetic exchange between arrangements has not been high enough to homogenize nucleotide variation in the center of the A2 inversion. A2 can be considered a typical successful inversion of D. subobscura according to its relative length. Chromosomal inversion polymorphism of D. subobscura might thus cause the genome of this species to be highly structured and to harbor different gene pools that might contribute to maintain adaptations to particular environments.