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Quantitative profiling of BATF family proteins/JUNB/IRF hetero-trimers using Spec-seq

机译:使用Spec-seq对BATF家族蛋白/ JUNB / IRF异三聚体进行定量分析

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摘要

BackgroundBATF family transcription factors (BATF, BATF2 and BATF3) form hetero-trimers with JUNB and either IRF4 or IRF8 to regulate cell fate in T cells and dendritic cells in vivo. While each combination of the hetero-trimer has a distinct role, some degree of cross-compensation was observed. The basis for the differential actions of IRF4 and IRF8 with BATF factors and JUNB is still unknown. We propose that the differences in function between these hetero-trimers may be caused by differences in their DNA binding preferences. While all three BATF family transcription factors have similar binding preferences when binding as a hetero-dimer with JUNB, the cooperative binding of IRF4 or IRF8 to the hetero-dimer/DNA complex could change the preferences. We used Spec-seq, which allows for the efficient and accurate determination of relative affinity to a large collection of sequences in parallel, to find differences between cooperative DNA binding of IRF4, IRF8 and BATF family members.
机译:背景BATF家族转录因子(BATF,BATF2和BATF3)与JUNB和IRF4或IRF8形成异源三聚体,以调节体内T细胞和树突状细胞的命运。尽管异三聚体的每种组合具有不同的作用,但观察到一定程度的交叉补偿。带有BATF因子和JUNB的IRF4和IRF8差异作用的基础仍然未知。我们建议这些异三聚体之间的功能差异可能是由其DNA结合偏好的差异引起的。虽然所有三个BATF家族转录因子在与JUNB异源二聚体结合时都具有相似的结合偏好,但IRF4或IRF8与异源二聚体/ DNA复合体的协同结合可能会改变偏好。我们使用Spec-seq(Spec-seq)可以有效,准确地确定与大量平行序列的相对亲和力,以发现IRF4,IRF8和BATF家族成员的合作DNA结合之间的差异。

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