Allele-specific population structure of Drosophila melanogaster alcohol dehydrogenase at the molecular level

29Citations
Citations of this article
18Readers
Mendeley users who have this article in their library.
Get full text

Abstract

The history of the Drosophila melanogaster alcohol dehydrogenase (ADH) Fast/Slow polymorphism was studied by recording molecular variation and inversion polymorphism in 233 chromosomes from European and African populations. Silent molecular variation in the Slow allele was very different between standard chromosomes and chromosomes bearing the In(2L)t inversion. Within populations, inverted Slow haplotypes were more variable than standard Slow haplotypes. Between populations, geographical structure was almost nonexistent for inverted Slow haplotypes and highly significant for standard Slow. All Fast haplotypes occurred on standard chromosomes. They showed little variation within and between populations. They were highly significantly closer to standard Slow haplotypes from Europe. These results suggest that the current range of Fast and In(2L)t Slow haplotypes is recent and that an older genetic differentiation between populations was followed by allele-specific gene flow.

Cite

CITATION STYLE

APA

Veuille, M., Bénassi, V., Aulard, S., & Depaulis, F. (1998). Allele-specific population structure of Drosophila melanogaster alcohol dehydrogenase at the molecular level. Genetics, 149(2), 971–981. https://doi.org/10.1093/genetics/149.2.971

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free