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Context-dependent DNA recognition code for C2H2 zinc-finger transcription factors

机译:C2H2锌指转录因子的上下文相关DNA识别代码

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Motivation: Modeling and identifying the DNA-protein recognition code is one of the most challenging problems in computational biology. Several quantitative methods have been developed to model DNA-protein interactions with specific focus on the C2H2 zinc-finger proteins, the largest transcription factor family in eukaryotic genomes. In many cases, they performed well. But the overall the predictive accuracy of these methods is still limited. One of the major reasons is all these methods used weight matrix models to represent DNA-protein interactions, assuming all base-amino acid contacts contribute independently to the total free energy of binding.Results: We present a context-dependent model for DNA-zinc-finger protein interactions that allows us to identify inter-positional dependencies in the DNA recognition code for C2H2 zinc-finger proteins. The degree of non-independence was detected by comparing the linear perceptron model with the non-linear neural net (NN) model for their predictions of DNA-zinc-finger protein interactions. This dependency is supported by the complex base-amino acid contacts observed in DNA-zinc-finger interactions from structural analyses. Using extensive published qualitative and quantitative experimental data, we demonstrated that the context-dependent model developed in this study can significantly improves predictions of DNA binding profiles and free energies of binding for both individual zinc fingers and proteins with multiple zinc fingers when comparing to previous positional-independent models. This approach can be extended to other protein families with complex base-amino acid residue interactions that would help to further understand the transcriptional regulation in eukaryotic genomes.
机译:动机:建模和识别DNA-蛋白质识别代码是计算生物学中最具挑战性的问题之一。已经开发了几种定量方法来建模DNA-蛋白质相互作用,特别是针对C2H2锌指蛋白,这是真核基因组中最大的转录因子家族。在许多情况下,他们的表现都不错。但是这些方法的总体预测准确性仍然有限。主要原因之一是所有这些方法都使用重量矩阵模型来表示DNA-蛋白质相互作用,假设所有碱基-氨基酸接触均独立地对结合的总自由能作出贡献。结果:我们提出了一种上下文相关的DNA-锌模型指蛋白相互作用,使我们能够识别C2H2锌指蛋白的DNA识别代码中的位置间依赖性。通过比较线性感知器模型和非线性神经网络(NN)模型对DNA-锌-指蛋白相互作用的预测,可以检测非独立程度。这种依赖性得到结构分析中DNA-锌-指相互作用中观察到的复杂的碱基-氨基酸接触的支持。使用大量已发表的定性和定量实验数据,我们证明了与先前的定位相比,本研究开发的上下文相关模型可以显着改善单个锌指和具有多个锌指的蛋白质的DNA结合谱和结合自由能的预测独立模型。这种方法可以扩展到具有复杂的碱基氨基酸残基相互作用的其他蛋白质家族,这将有助于进一步了解真核基因组中的转录调控。

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