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Global dynamics of stage-specific transcription factor binding during thymocyte development

机译:胸腺细胞发育过程中阶段特异性转录因子结合的全局动态

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In vertebrates, multiple transcription factors (TFs) bind to gene regulatory elements (promoters, enhancers, and silencers) to execute developmental expression changes. ChIP experiments are often used to identify where TFs bind to regulatory elements in the genome, but the requirement of TF-specific antibodies hampers analyses of tens of TFs at multiple loci. Here we tested whether TF binding predictions using ATAC-seq can be used to infer the identity of TFs that bind to functionally validated enhancers of the Cd4, Cd8, and Gata3 genes in thymocytes. We performed ATAC-seq at four distinct stages of development in mouse thymus, probing the chromatin accessibility landscape in double negative (DN), double positive (DP), CD4 single positive (SP4) and CD8 SP (SP8) thymocytes. Integration of chromatin accessibility with TF motifs genome-wide allowed us to infer stage-specific occupied TF binding sites within known and potentially novel regulatory elements. Our results provide genome-wide stage-specific T cell open chromatin profiles, and allow the identification of candidate TFs that drive thymocyte differentiation at each developmental stage.
机译:在脊椎动物中,多转录因子(TFS)与基因调节元素(启动子,增强剂和沉默物)结合以执行发育表达的变化。芯片实验通常用于鉴定TFS与基因组中的调节元件结合的位置,但TF特异性抗体的要求在多个基因座处分析了数十个TFS。在这里,我们测试了使用ATAC-SEQ的TF结合预测是否可用于推断与胸腺细胞中CD4,CD8和GATA3基因的功能验证增强剂结合的TFS的标识。我们在小鼠胸腺中的四个不同阶段进行ATAC-SEQ,探测双阴性(DN),双阳性(DP),CD4单阳性(SP4)和CD8 SP(SP8)胸腺细胞中的染色质辅助性景观。染色质可用性与TF基序的整合基因组允许我们在已知和潜在的新的调节元件中推断出特异性阶段的占用TF结合位点。我们的结果提供了基因组级特异性T细胞开放染色质曲线,并允许鉴定在每个发育阶段驱动胸腺细胞分化的候选TFS。

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