Lawniczak Mara K N, Holloway Alisha K, Begun David J, Jones Corbin D
Division of Cell and Molecular Biology, Imperial College London, London, SW7 2AZ, UK.
Genome Biol. 2008;9(8):R125. doi: 10.1186/gb-2008-9-8-r125. Epub 2008 Aug 12.
Understanding how DNA sequence polymorphism relates to variation in gene expression is essential to connecting genotypic differences with phenotypic differences among individuals. Addressing this question requires linking population genomic data with gene expression variation.
Using whole genome expression data and recent light shotgun genome sequencing of six Drosophila simulans genotypes, we assessed the relationship between expression variation in males and females and nucleotide polymorphism across thousands of loci. By examining sequence polymorphism in gene features, such as untranslated regions and introns, we find that genes showing greater variation in gene expression between genotypes also have higher levels of sequence polymorphism in many gene features. Accordingly, X-linked genes, which have lower sequence polymorphism levels than autosomal genes, also show less expression variation than autosomal genes. We also find that sex-specifically expressed genes show higher local levels of polymorphism and divergence than both sex-biased and unbiased genes, and that they appear to have simpler regulatory regions.
The gene-feature-based analyses and the X-to-autosome comparisons suggest that sequence polymorphism in cis-acting elements is an important determinant of expression variation. However, this relationship varies among the different categories of sex-biased expression, and trans factors might contribute more to male-specific gene expression than cis effects. Our analysis of sex-specific gene expression also shows that female-specific genes have been overlooked in analyses that only point to male-biased genes as having unusual patterns of evolution and that studies of sexually dimorphic traits need to recognize that the relationship between genetic and expression variation at these traits is different from the genome as a whole.
了解DNA序列多态性如何与基因表达变异相关联,对于将个体间的基因型差异与表型差异联系起来至关重要。解决这个问题需要将群体基因组数据与基因表达变异联系起来。
利用全基因组表达数据以及对六种拟果蝇基因型进行的近期轻量级鸟枪法基因组测序,我们评估了雄性和雌性的表达变异与数千个位点的核苷酸多态性之间的关系。通过检查基因特征(如非翻译区和内含子)中的序列多态性,我们发现基因型间基因表达差异较大的基因,在许多基因特征中也具有较高水平的序列多态性。因此,与常染色体基因相比,序列多态性水平较低的X连锁基因,其表达变异也比常染色体基因少。我们还发现,性别特异性表达的基因比性别偏向和无偏向的基因表现出更高的局部多态性和分歧水平,并且它们似乎具有更简单的调控区域。
基于基因特征的分析以及X染色体与常染色体的比较表明,顺式作用元件中的序列多态性是表达变异的一个重要决定因素。然而,这种关系在不同类别的性别偏向表达中有所不同,并且反式因子对雄性特异性基因表达的贡献可能比顺式效应更大。我们对性别特异性基因表达的分析还表明,在仅指出雄性偏向基因具有异常进化模式的分析中,雌性特异性基因被忽视了,并且对两性异形性状的研究需要认识到,这些性状的遗传与表达变异之间的关系与整个基因组不同。