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Genome-wide binding studies reveal DNA binding specificity mechanisms and functional interplay amongst Forkhead transcription factors

机译:全基因组结合研究揭示了叉头转录因子之间的DNA结合特异性机制和功能相互作用

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摘要

Transcription factors belonging to the same transcription factor families contain very similar DNA binding domains and hence have the potential to bind to related DNA sequences. However, subtle differences in binding specificities can be detected in vitro with the potential to direct specific responses in vivo. Here, we have examined the binding properties of three Forkhead (FOX) transcription factors, FOXK2, FOXO3 and FOXJ3 in vivo. Extensive overlap in chromatin binding is observed, although underlying differential DNA binding specificity can dictate the recruitment of FOXK2 and FOXJ3 to chromatin. However, functionally, FOXO3-dependent gene regulation is generally mediated not through uniquely bound regions but through regions occupied by both FOXK2 and FOXO3 where both factors play a regulatory role. Our data point to a model whereby FOX transcription factors control gene expression through dynamically binding and generating partial occupancy of the same site rather than mutually exclusive binding derived by stable binding of individual FOX proteins.
机译:属于相同转录因子家族的转录因子包含非常相似的DNA结合结构域,因此具有与相关DNA序列结合的潜力。但是,可以在体外检测到结合特异性的细微差异,有可能在体内指导特异性反应。在这里,我们已经检查了三种Forkhead(FOX)转录因子,FOXK2,FOXO3和FOXJ3在体内的结合特性。观察到染色质结合的广泛重叠,尽管潜在的DNA差异结合特异性可能决定FOXK2和FOXJ3向染色质的募集。但是,在功能上,FOXO3依赖性基因调节通常不是通过唯一结合的区域介导,而是通过FOXK2和FOXO3两者占据的区域介导,在这两个因素均起调节作用。我们的数据指向一个模型,在该模型中,FOX转录因子通过动态结合并产生相同位点的部分占有而不是通过单个FOX蛋白的稳定结合而产生的互斥结合来控制基因表达。

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