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Rearrangements of 2.5 Kilobases of Noncoding DNA from the Drosophila even-skipped Locus Define Predictive Rules of Genomic cis-Regulatory Logic

机译:果蝇均匀跳过基因座的非编码DNA的2.5个碱基的重排定义了基因组顺式调控逻辑的预测规则。

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摘要

Rearrangements of about 2.5 kilobases of regulatory DNA located 5′ of the transcription start site of the Drosophila even-skipped locus generate large-scale changes in the expression of even-skipped stripes 2, 3, and 7. The most radical effects are generated by juxtaposing the minimal stripe enhancers MSE2 and MSE3 for stripes 2 and 3 with and without small “spacer” segments less than 360 bp in length. We placed these fusion constructs in a targeted transformation site and obtained quantitative expression data for these transformants together with their controlling transcription factors at cellular resolution. These data demonstrated that the rearrangements can alter expression levels in stripe 2 and the 2–3 interstripe by a factor of more than 10. We reasoned that this behavior would place tight constraints on possible rules of genomic cis-regulatory logic. To find these constraints, we confronted our new expression data together with previously obtained data on other constructs with a computational model. The model contained representations of thermodynamic protein–DNA interactions including steric interference and cooperative binding, short-range repression, direct repression, activation, and coactivation. The model was highly constrained by the training data, which it described within the limits of experimental error. The model, so constrained, was able to correctly predict expression patterns driven by enhancers for other Drosophila genes; even-skipped enhancers not included in the training set; stripe 2, 3, and 7 enhancers from various Drosophilid and Sepsid species; and long segments of even-skipped regulatory DNA that contain multiple enhancers. The model further demonstrated that elevated expression driven by a fusion of MSE2 and MSE3 was a consequence of the recruitment of a portion of MSE3 to become a functional component of MSE2, demonstrating that cis-regulatory “elements” are not elementary objects.
机译:位于果蝇均匀跳跃基因座转录起始位点5'处的约2.5 kb的调节DNA的重排会产生均匀跳跃的条带2、3和7的表达发生大规模变化。将带有和不带有长度小于360 bp的小“间隔”段的条2和3的最小条增强子MSE2和MSE3并置。我们将这些融合构建体置于目标转化位点,并在细胞分辨率下获得了这些转化体及其控制转录因子的定量表达数据。这些数据表明,重排可以改变条带2和2–3条纹中的表达水平超过10倍。我们认为,这种行为将对基因组顺式调控逻辑的可能规则施加严格的约束。为了找到这些约束,我们将新的表达式数据与先前获得的关于具有计算模型的其他构造的数据一起使用。该模型包含热力学蛋白质与DNA相互作用的表示,包括空间干扰和协同结合,短程抑制,直接抑制,激活和共激活。该模型受到训练数据的严格约束,该训练数据在实验误差的范围内进行了描述。这样受限制的模型能够正确预测由其他果蝇基因的增强子驱动的表达模式。训练集中未包括的均匀跳过的增强剂;来自各种果蝇和败血症物种的条纹2、3和7增强子;以及含有多种增强子的长段均匀调节DNA。该模型进一步证明,由MSE2和MSE3融合驱动的表达升高是一部分MSE3募集成为MSE2的功能性成分的结果,表明顺式调控“元素”不是基本对象。

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