Department of Biology, Texas A&M University, College Station, TX, USA.
BMC Genomics. 2009 Dec 3;10:579. doi: 10.1186/1471-2164-10-579.
In many taxa, males and females are very distinct phenotypically, and these differences often reflect divergent selective pressures acting on the sexes. Phenotypic sexual dimorphism almost certainly reflects differing patterns of gene expression between the sexes, and microarray studies have documented widespread sexually dimorphic gene expression. Although the evolutionary significance of sexual dimorphism in gene expression remains unresolved, these studies have led to the formulation of a hypothesis that male-driven evolution has resulted in the masculinization of animal transcriptomes. Here we use a microarray assessment of sex- and gonad-biased gene expression to test this hypothesis in zebrafish.
By using zebrafish Affymetrix microarrays to compare gene expression patterns in male and female somatic and gonadal tissues, we identified a large number of genes (5899) demonstrating differences in transcript abundance between male and female Danio rerio. Under conservative statistical significance criteria, all sex-biases in gene expression were due to differences between testes and ovaries. Male-enriched genes were more abundant than female-enriched genes, and expression bias for male-enriched genes was greater in magnitude than that for female-enriched genes. We also identified a large number of genes demonstrating elevated transcript abundance in testes and ovaries relative to male body and female body, respectively.
Overall our results support the hypothesis that male-biased evolutionary pressures have resulted in male-biased patterns of gene expression. Interestingly, our results seem to be at odds with a handful of other microarray-based studies of sex-specific gene expression patterns in zebrafish. However, ours was the only study designed to address this specific hypothesis, and major methodological differences among studies could explain the discrepancies. Regardless, all of these studies agree that transcriptomic sex differences in D. rerio are widespread despite the apparent absence of heterogamety. These differences likely make important contributions to phenotypic sexual dimorphism in adult zebrafish; thus, from an evolutionary standpoint, the precise roles of sex-specific selection and sexual conflict in the evolution of sexually dimorphic gene expression are very important. The results of our study and others like it set the stage for further work aimed at directly addressing this exciting issue in comparative genomics.
在许多分类群中,雄性和雌性在表型上非常不同,这些差异通常反映了对两性施加的不同选择压力。表型性别二态性几乎肯定反映了两性之间基因表达模式的不同,而微阵列研究已经记录了广泛的性别二态性基因表达。虽然性别二态性在基因表达中的进化意义仍未解决,但这些研究导致了一个假设的形成,即雄性驱动的进化导致了动物转录组的雄性化。在这里,我们使用微阵列评估性别和性腺偏倚的基因表达,以在斑马鱼中检验这一假设。
通过使用斑马鱼 Affymetrix 微阵列比较雄性和雌性体组织和性腺组织中的基因表达模式,我们鉴定了大量在 Danio rerio 中表现出转录丰度差异的基因(5899 个)。在保守的统计显著性标准下,所有基因表达的性别偏倚都归因于睾丸和卵巢之间的差异。雄性富集基因比雌性富集基因更丰富,雄性富集基因的表达偏倚程度大于雌性富集基因。我们还鉴定了大量在睾丸和卵巢中表达丰度高于雄性体和雌性体的基因。
总的来说,我们的结果支持了这样的假设,即雄性偏倚的进化压力导致了雄性偏倚的基因表达模式。有趣的是,我们的结果似乎与其他少数几项基于微阵列的斑马鱼性别特异性基因表达模式研究不一致。然而,我们的研究是唯一旨在解决这一特定假设的研究,研究之间的主要方法学差异可能解释了差异。无论如何,所有这些研究都同意,尽管缺乏异型配子,但 D. rerio 的转录组性别差异是广泛存在的。这些差异可能对成年斑马鱼的表型性别二态性做出重要贡献;因此,从进化的角度来看,性别特异性选择和性冲突在性别二态性基因表达进化中的精确作用非常重要。我们的研究结果和其他类似研究为进一步的工作奠定了基础,旨在在比较基因组学中直接解决这一令人兴奋的问题。