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Using protein-binding microarrays to study transcription factor specificity: homologs isoforms and complexes

机译:使用蛋白质结合微阵列研究转录因子特异性:同源物同工型和复合物

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摘要

Protein–DNA binding is central to specificity in gene regulation, and methods for characterizing transcription factor (TF)–DNA binding remain crucial to studies of regulatory specificity. High-throughput (HT) technologies have revolutionized our ability to characterize protein–DNA binding by significantly increasing the number of binding measurements that can be performed. Protein-binding microarrays (PBMs) are a robust and powerful HT platform for studying DNA-binding specificity of TFs. Analysis of PBM-determined DNA-binding profiles has provided new insight into the scope and mechanisms of TF binding diversity. In this review, we focus specifically on the PBM technique and discuss its application to the study of TF specificity, in particular, the binding diversity of TF homologs and multi-protein complexes.
机译:蛋白质-DNA结合是基因调控中特异性的关键,表征转录因子(TF)-DNA结合的方法对于调控特异性的研究仍然至关重要。高通量(HT)技术通过显着增加可进行结合测量的次数,彻底改变了我们表征蛋白质与DNA结合的能力。蛋白质结合微阵列(PBM)是一个强大而强大的HT平台,用于研究TF的DNA结合特异性。 PBM确定的DNA绑定配置文件的分析提供了对TF绑定多样性的范围和机制的新见解。在这篇综述中,我们特别关注PBM技术,并讨论其在TF特异性研究中的应用,尤其是TF同源物和多蛋白复合物的结合多样性。

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