Both naturally occurring insertions of transposable elements and intermediate frequency polymorphisms at the achaete-scute complex are associated with variation in bristle number in Drosophila melanogaster

Citation
Ad. Long et al., Both naturally occurring insertions of transposable elements and intermediate frequency polymorphisms at the achaete-scute complex are associated with variation in bristle number in Drosophila melanogaster, GENETICS, 154(3), 2000, pp. 1255-1269
Citations number
45
Categorie Soggetti
Biology,"Molecular Biology & Genetics
Journal title
GENETICS
ISSN journal
00166731 → ACNP
Volume
154
Issue
3
Year of publication
2000
Pages
1255 - 1269
Database
ISI
SICI code
0016-6731(200003)154:3<1255:BNOIOT>2.0.ZU;2-6
Abstract
A restriction enzyme survey of a 110-kb region including the achaete scute complex (ASC) examined 14 polymorphic molecular markers in a sample of 56 n aturally occurring chromosomes. Large insertions as a class were associated with a reduction in both sternopleural and abdominal bristle number, suppo rting deleterious mutation-selection equilibrium models Tol the maintenance of quantitative generic variation. Two polymorphic sites were independentl y associated with variation in bristle number measured in two genetic backg rounds as assessed by a permutation test. A 6-bp deletion near sc alpha is associated with sternopleural bristle number variation in both sexes and a 3.4-kb insertion between sc beta and sc gamma is associated with abdominal bristle number variation in females. Under an additive genetic model, the s mall deletion polymorphism near sc alpha accounts for 25% of the total X ch romosome genetic variation in sternopleural bristle number, and the 3.4 kb insertion accounts for 22% of the total X chromosome variation in female ab dominal bristle number. The observation of common polymorphisms associated with variation in bristle number is more parsimoniously; explained by model s that incorporate balancing selection or assume variants affecting bristle number are neutral, than mutation-selection equilibrium models.