Department of Biology, The Pennsylvania State University, 208 Erwin W. Mueller Laboratory, University Park, PA 16802-5301, USA.
Human Genome Sequencing Center, Baylor College of Medicine, One Baylor Plaza, Houston, TX 77030, USA.
G3 (Bethesda). 2024 Oct 7;14(10). doi: 10.1093/g3journal/jkae176.
When adaptive phenotypic variation or quantitative trait loci map within an inverted segment of a chromosome, researchers often despair because the suppression of crossing over will prevent the discovery of selective target genes that established the rearrangement. If an inversion polymorphism is old enough, then the accumulation of gene conversion tracts offers the promise that quantitative trait loci or selected loci within inversions can be mapped. The inversion polymorphism of Drosophila pseudoobscura is a model system to show that gene conversion analysis is a useful tool for mapping selected loci within inversions. D. pseudoobscura has over 30 different chromosomal arrangements on the third chromosome (Muller C) in natural populations and their frequencies vary with changes in environmental habitats. Statistical tests of five D. pseudoobscura gene arrangements identified outlier genes within inverted regions that had potentially heritable variation, either fixed amino acid differences or differential expression patterns. We use genome sequences of the inverted third chromosome (Muller C) to infer 98,443 gene conversion tracts for a total coverage of 142 Mb or 7.2× coverage of the 19.7 Mb chromosome. We estimated gene conversion tract coverage in the 2,668 genes on Muller C and tested whether gene conversion coverage was similar among arrangements for outlier vs non-outlier loci. Outlier genes had lower gene conversion tract coverage among arrangements than the non-outlier genes suggesting that selection removes exchanged DNA in the outlier genes. These data support the hypothesis that the third chromosome in D. pseudoobscura captured locally adapted combinations of alleles prior to inversion mutation events.
当适应性表型变异或数量性状基因座映射到染色体的倒位片段内时,研究人员常常感到绝望,因为交叉抑制会阻止发现建立重排的选择性靶基因。如果倒位多态性足够古老,那么基因转换片段的积累就有望对倒位中的数量性状基因座或选择基因座进行定位。果蝇拟暗褐果蝇的倒位多态性是一个模型系统,表明基因转换分析是定位倒位中选择基因座的有用工具。在自然种群中,果蝇拟暗褐果蝇的第三号染色体(Muller C)上有超过 30 种不同的染色体排列,其频率随环境栖息地的变化而变化。对五个果蝇拟暗褐果蝇基因排列的统计检验鉴定出了倒位区域内的异常基因,这些基因具有潜在的可遗传变异,要么是固定的氨基酸差异,要么是差异表达模式。我们使用倒置的第三号染色体(Muller C)的基因组序列来推断 98,443 个基因转换片段,总覆盖率为 142Mb,或 19.7Mb 染色体的 7.2×覆盖率。我们估计了 Muller C 上 2668 个基因的基因转换片段覆盖率,并测试了异常和非异常基因座的排列中基因转换片段覆盖率是否相似。与非异常基因相比,异常基因在排列中的基因转换片段覆盖率较低,这表明选择去除了异常基因中的交换 DNA。这些数据支持了这样一种假设,即在果蝇拟暗褐果蝇中,第三号染色体在倒位突变事件之前捕获了局部适应的等位基因组合。