Department of Ecology and Evolutionary Biology, University of Toronto, Toronto, ON, Canada M5S 3B2.
Department of Molecular Biosciences, The Wenner-Gren Institute, Stockholm University, Stockholm SE-10691, Sweden.
Genome Biol Evol. 2024 Nov 1;16(11). doi: 10.1093/gbe/evae234.
Much of sexual dimorphism is likely due to sex-biased gene expression, which results from differential regulation of a genome that is largely shared between males and females. Here, we use allele-specific expression to explore cis-regulatory variation in Drosophila melanogaster in relation to sex. We develop a Bayesian framework to infer the transcriptome-wide joint distribution of cis-regulatory effects across the sexes. We also examine patterns of cis-regulatory variation with respect to two other levels of variation in sexual dimorphism: (i) across genes that vary in their degree of sex-biased expression and (ii) among tissues that vary in their degree of dimorphism (e.g. relatively low dimorphism in heads vs. high dimorphism in gonads). We uncover evidence of widespread cis-regulatory variation in all tissues examined, with female-biased genes being especially enriched for this variation. A sizeable proportion of cis-regulatory variation is inferred to have sex-specific effects, with sex-dependent cis effects being much more frequent in gonads than in heads. Finally, we find some genes where 1 allele contributes to more than 50% of a gene's expression in heterozygous males but <50% of its expression in heterozygous females. Such variants could provide a mechanism for sex-specific dominance reversals, a phenomenon important for sexually antagonistic balancing selection. However, tissue differences in allelic imbalance are approximately as frequent as sex differences, perhaps suggesting that sexual conflict may not be particularly unique in shaping patterns of expression variation.
许多性二型现象可能归因于性偏向基因表达,这是由于大部分在雌雄两性中共享的基因组受到差异调控所致。在这里,我们使用等位基因特异性表达来探究黑腹果蝇中与性别有关的顺式调控变异。我们开发了一种贝叶斯框架来推断整个转录组中跨性别的顺式调控效应的联合分布。我们还研究了顺式调控变异与性二型性的另外两个层面的关系:(i)在基因的表达程度上存在性别偏向的差异,(ii)在组织中存在性别二型性的差异(例如头部的性别二型性相对较低,而性腺的性别二型性较高)。我们发现所有检查的组织中都存在广泛的顺式调控变异,雌性偏向的基因尤其富含这种变异。推断出相当一部分顺式调控变异具有性别特异性效应,并且在性腺中与在头部相比,性别依赖的顺式效应更为频繁。最后,我们发现了一些基因,在杂合雄性中,1 个等位基因对基因表达的贡献超过 50%,而在杂合雌性中,其表达不到 50%。这种变异可能为性别特异性显性反转提供了一种机制,这是一种对性拮抗平衡选择很重要的现象。然而,等位基因失衡的组织差异与性别差异大致相同,这可能表明性冲突在塑造表达变异模式方面并非特别独特。