Fear Justin M, León-Novelo Luis G, Morse Alison M, Gerken Alison R, Van Lehmann Kjong, Tower John, Nuzhdin Sergey V, McIntyre Lauren M
Molecular Genetics and Microbiology, University of Florida, Gainesville, Florida 32611 Genetics Institute, University of Florida, Gainesville, Florida 32611.
Department of Biostatistics, University of Texas Health Science Center at Houston-School of Public Health, Houston, Texas 77030.
Genetics. 2016 Jul;203(3):1177-90. doi: 10.1534/genetics.116.188797. Epub 2016 May 18.
Regulatory variation in gene expression can be described by cis- and trans-genetic components. Here we used RNA-seq data from a population panel of Drosophila melanogaster test crosses to compare allelic imbalance (AI) in female head tissue between mated and virgin flies, an environmental change known to affect transcription. Indeed, 3048 exons (1610 genes) are differentially expressed in this study. A Bayesian model for AI, with an intersection test, controls type I error. There are ∼200 genes with AI exclusively in mated or virgin flies, indicating an environmental component of expression regulation. On average 34% of genes within a cross and 54% of all genes show evidence for genetic regulation of transcription. Nearly all differentially regulated genes are affected in cis, with an average of 63% of expression variation explained by the cis-effects. Trans-effects explain 8% of the variance in AI on average and the interaction between cis and trans explains an average of 11% of the total variance in AI. In both environments cis- and trans-effects are compensatory in their overall effect, with a negative association between cis- and trans-effects in 85% of the exons examined. We hypothesize that the gene expression level perturbed by cis-regulatory mutations is compensated through trans-regulatory mechanisms, e.g., trans and cis by trans-factors buffering cis-mutations. In addition, when AI is detected in both environments, cis-mated, cis-virgin, and trans-mated-trans-virgin estimates are highly concordant with 99% of all exons positively correlated with a median correlation of 0.83 for cis and 0.95 for trans We conclude that the gene regulatory networks (GRNs) are robust and that trans-buffering explains robustness.
基因表达中的调控变异可由顺式和反式遗传成分来描述。在此,我们利用黑腹果蝇测交群体面板的RNA测序数据,比较了交配雌蝇和未交配雌蝇头部组织中的等位基因失衡(AI),已知这种环境变化会影响转录。事实上,在本研究中有3048个外显子(1610个基因)存在差异表达。一种用于AI的贝叶斯模型,通过交叉检验来控制I型错误。有大约200个基因仅在交配或未交配的果蝇中存在AI,这表明表达调控存在环境成分。在一个杂交组合中,平均34%的基因以及所有基因的54%显示出转录受到遗传调控的证据。几乎所有差异调控的基因都受到顺式影响,平均63%的表达变异由顺式效应解释。反式效应平均解释AI变异的8%,顺式和反式之间的相互作用平均解释AI总变异的11%。在两种环境中,顺式和反式效应在总体效应上是补偿性的,在所检测的85%的外显子中,顺式和反式效应呈负相关。我们推测,由顺式调控突变扰乱的基因表达水平通过反式调控机制得到补偿,例如通过反式因子缓冲顺式突变来实现反式和顺式补偿。此外,当在两种环境中都检测到AI时,顺式交配、顺式未交配以及反式交配 - 反式未交配的估计值高度一致,99%的所有外显子呈正相关,顺式的中位数相关性为0.83,反式的中位数相关性为0.95。我们得出结论,基因调控网络(GRNs)是稳健的,并且反式缓冲解释了这种稳健性。