Abstract

Many agriculturally, evolutionarily, and medically important characters vary in a quantitative fashion. Unfortunately, the genes and sequence variants accounting for this variation remain largely unknown due to a variety of biological and technical challenges. Drosophila melanogaster contains high levels of sequence variation and low linkage disequilibrium, allowing us to dissect the effects of many causative variants within a single locus. Here, we take advantage of these features to identify and characterize the sequence polymorphisms that comprise major effect QTL alleles segregating at the bric-a-brac locus. We show that natural bric-a-brac alleles with large effects on cuticular pigmentation reflect a cumulative impact of polymorphisms that affect three functional regions: a promoter, a tissue-specific enhancer, and a Polycomb response element. Analysis of allele-specific expression at the bric-a-brac locus confirms that these polymorphisms modulate transcription at the cis-regulatory level. Our results establish that a single QTL can act through a confluence of multiple molecular mechanisms and that sequence variation in regions flanking experimentally validated functional elements can have significant quantitative effects on transcriptional activity and phenotype. These findings have important design and conceptual implications for basic and medical genomics.

Highlights

  • Quantitative trait loci (QTLs) have traditionally been identified by linkage analysis in experimental crosses [1]

  • These methods have been advanced with creative applications [3,4], but in most cases QTL regions have only been narrowed to a single gene

  • Linkage disequilibrium (LD) at the bab locus extends for less than 1 kb, [10] providing an opportunity to dissect the causative nucleotide variation that contributes to the cumulative effect of QTL alleles

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Summary

Introduction

Quantitative trait loci (QTLs) have traditionally been identified by linkage analysis in experimental crosses [1]. We take a QTL study to its logical conclusion by describing the fine structure of functional variation that underlies large-effect QTL alleles segregating in a natural population To meet this aim, we sequenced the 148 kb bric a brac (bab) genomic region from 94 inbred lines of D. melanogaster sampled from a single location. Previous analysis revealed evidence of directional selection in two regions within the bab locus, including the previously identified cis-regulatory element (CRE) that controls sex-specific abdominal pigmentation [8,10] This confluence of population- and developmental-genetic evidence sets the stage for connecting specific DNA polymorphisms to variation in gene expression and, in phenotypic traits.

Author Summary
Findings
Materials and Methods

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