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Heterodimeric DNA motif synthesis and validations

机译:异二聚体DNA基序合成和验证

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摘要

Bound by transcription factors, DNA motifs (i.e. transcription factor binding sites) are prevalent and important for gene regulation in different tissues at different developmental stages ofeukaryotes. Although considerable efforts have been made on elucidating monomeric DNA motif patterns, our knowledge on heterodimeric DNA motifs are still far from complete. Therefore, we propose to develop a computational approach to synthesize a heterodimeric DNA motif from two monomeric DNA motifs. The approach is sequentially divided into two components (Phases A and B). In Phase A, we propose to develop the inference models on how two DNA monomeric motifs can be oriented and overlapped with each other at nucleotide level. In Phase B, given the two monomeric DNA motifs oriented, we further propose to develop DNA-binding family-specific input-output hidden Markov models (IOHMMs) to synthesize a heterodimeric DNA motif. To validate the approach, we execute and cross-validate it with the experimentally verified 618 heterodimeric DNA motifs across 49 DNA-binding family combinations. We observe that our approach can even rescue" the existing heterodimeric DNA motif pattern (i.e. HOXB2_EOMES) previously published on Nature. Lastly, we apply the proposed approach to infer previously uncharacterized heterodimeric motifs. Their motif instances are supported by DNase accessibility, gene ontology, protein-protein interactions, in vivo ChIP-seq peaks, and even structural data from PDB. A public web-server is built for open accessibility and scientific impact. Its address is listed as follows: http://motif.cs.cityu.edu.hk/custom/MotifKirin.
机译:通过转录因子的结合,DNA基序(即转录因子结合位点)是普遍的,对不同组织的基因调节是普遍的,重要的是在不同的发育阶段的不同组织中。虽然已经对阐明单体DNA主题图案进行了相当大的努力,但我们对杂二种DNA主题的了解仍然远未完成。因此,我们建议开发一种计算方法来合成来自两种单体DNA基序的异二聚酯DNA基序。该方法被顺序分为两种组分(阶段A和B)。在A阶段,我们建议在核苷酸水平下,在两种DNA单体基序如何彼此相互定向和重叠的推理模型。在B相中,给出了取向的两种单体DNA基序,我们进一步提出开发DNA结合的家庭特异性输入输出隐马尔可夫模型(IOHMMS)以合成异二聚体DNA基序。为了验证方法,我们通过通过49个DNA结合家族组合的实验验证的618异二聚酯DNA基序来执行和交叉验证。我们观察到我们的方法甚至可以拯救“现有的异二聚酯DNA基序模式(即Hoxb2_eomes)以前发表于自然界。最后,我们应用所提出的方法来推断出先前无表的异二聚体图案。它们的主题实例由DNase可访问性,基因本体,基因本体支持,蛋白质 - 蛋白质相互作用,体内芯片-SEQ峰值,甚至来自PDB的结构数据。用于开放访问和科学影响,构建了公共网络服务器。其地址如下所示:http://motif.cs.cityu。 edu.hk/custom/motifkirin。

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  • 来源
    《Nucleic Acids Research》 |2019年第4期|共9页
  • 作者单位

    City Univ Hong Kong Dept Comp Sci Kowloon Tong Hong Kong Peoples R China;

    City Univ Hong Kong Dept Comp Sci Kowloon Tong Hong Kong Peoples R China;

    City Univ Hong Kong Dept Comp Sci Kowloon Tong Hong Kong Peoples R China;

    Shenzhen Univ Coll Comp Sci &

    Software Engn Shenzhen Peoples R China;

    Shandong Normal Univ Sch Informat Sci &

    Engn Jinan Shandong Peoples R China;

    Univ Hong Kong Sch Biomed Sci Pokfulam Hong Kong Peoples R China;

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  • 正文语种 eng
  • 中图分类 生物化学;
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