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Assessing constraints on the path of regulatory sequence evolution

机译:评估对调控序列进化路径的限制

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摘要

Structural and functional constraints are known to play a major role in restricting the path of evolution of protein activities. However, constraints acting on evolving transcriptional regulatory sequences, e.g. enhancers, are largely unknown. Recently, we elucidated how a novel expression pattern of the Neprilysin-1 (Nep1) gene in the optic lobe of Drosophila santomea evolved via co-option of existing enhancer activities. Drosophila santomea, which has diverged from Drosophila yakuba by approximately 400 000 years has accumulated four fixed mutations that each contribute to the full activity of this enhancer. Recreating and testing the optic lobe enhancer of the ancestor of D. santomea and D. yakuba revealed that the strong D. santomea enhancer activity evolved from a weak ancestral activity. Because each mutation on the path from the D. yakuba/santomea ancestor to modern-day D. santomea contributes to the newly derived optic lobe enhancer activity, we sought here to use this system to study the path of evolution of enhancer sequences. We inferred likely paths of evolution of this enhancer by observing the transcriptional output of all possible intermediate steps between the ancestral D. yakuba/santomea enhancer and the modern D. santomea enhancer. Many possible paths had epistatic and cooperative effects. Furthermore, we found that several paths significantly increased ectopic transcriptional activity or affected existing enhancer activities from which the novel activity was co-opted. We suggest that these attributes highlight constraints that guide the path of evolution of enhancers.
机译:已知结构和功能限制在限制蛋白质活性进化途径中起主要作用。但是,限制作用于进化的转录调控序列,例如。增强剂,很大程度上未知。最近,我们阐明了果蝇果蝇视神经叶中Neprilysin-1(Nep1)基因的新型表达模式是如何通过共同选择现有增强子活性来进化的。与果蝇雅库巴分离大约40万年的果蝇果蝇已经积累了四个固定的突变,每个突变都有助于这种增强子的全部活性。重建和测试D. santomea和D. yakuba祖先的视神经叶增强剂表明,强大的D. santomea增强剂活性是由较弱的祖先活性演变而来。因为从雅库芭氏菌/ antomea祖先到现代D. santomea的路径上的每个突变都有助于新近衍生的视叶增强子活性,所以我们在这里寻求使用该系统来研究增强子序列的进化路径。我们通过观察祖先的d。yakuba / santomea增强子和现代D. santomea增强子之间所有可能的中间步骤的转录输出,推断了该增强子的进化途径。许多可能的途径具有上位性和协同作用。此外,我们发现几种途径可以显着增加异位转录活性或影响现有的增强子活性,从中可以选择新的活性。我们建议这些属性突出显示了指导增强子进化路径的约束。

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