黑腹果蝇性别和两性异形的顺式调控变异。

IF 3.2 2区 生物学 Q2 EVOLUTIONARY BIOLOGY Genome Biology and Evolution Pub Date : 2024-11-01 DOI:10.1093/gbe/evae234
Prashastha Mishra, Tania S Barrera, Karl Grieshop, Aneil F Agrawal
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引用次数: 0

摘要

许多两性二态现象可能是由于性别偏倚的基因表达,这是由于基因组在很大程度上在男性和女性之间共享的差异调节造成的。在这里,我们使用等位基因特异性表达来探索黑腹果蝇与性别相关的顺式调控变异。我们开发了一个贝叶斯框架来推断顺式调节效应在跨性别的转录组范围内的联合分布。我们还研究了关于两性二态性的两个其他水平变异的顺式调控变异模式:(i)在性别偏性表达程度不同的基因之间,(ii)在二态性程度不同的组织之间(例如,头部二态性相对较低,性腺二态性较高)。我们发现在所检查的所有组织中普遍存在顺式调控变异的证据,其中女性偏倚基因尤其富集于这种变异。据推测,相当大比例的顺式调节变异具有性别特异性效应,性别依赖性顺式效应在性腺中比在头部中更为常见。最后,我们发现一些基因在杂合雄性中,一个等位基因对一个基因表达的贡献超过50%
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Cis-regulatory Variation in Relation to Sex and Sexual Dimorphism in Drosophila melanogaster.

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.

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来源期刊
Genome Biology and Evolution
Genome Biology and Evolution EVOLUTIONARY BIOLOGY-GENETICS & HEREDITY
CiteScore
5.80
自引率
6.10%
发文量
169
审稿时长
1 months
期刊介绍: About the journal Genome Biology and Evolution (GBE) publishes leading original research at the interface between evolutionary biology and genomics. Papers considered for publication report novel evolutionary findings that concern natural genome diversity, population genomics, the structure, function, organisation and expression of genomes, comparative genomics, proteomics, and environmental genomic interactions. Major evolutionary insights from the fields of computational biology, structural biology, developmental biology, and cell biology are also considered, as are theoretical advances in the field of genome evolution. GBE’s scope embraces genome-wide evolutionary investigations at all taxonomic levels and for all forms of life — within populations or across domains. Its aims are to further the understanding of genomes in their evolutionary context and further the understanding of evolution from a genome-wide perspective.
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