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High constitutive activity of a broad panel of housekeeping and tissue-specific cis-regulatory elements depends on a subset of ETS proteins

机译:大量管家和组织特异性顺式调控元件的高本构活性取决于ETS蛋白的子集

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摘要

Enhancers and promoters that control the transcriptional output of terminally differentiated cells include cell type-specific and broadly active housekeeping elements. Whether the high constitutive activity of these two groups of cis-regulatory elements relies on entirely distinct or instead also on shared regulators is unknown. By dissecting the cis-regulatory repertoire of macrophages, we found that the ELF subfamily of ETS proteins selectively bound within 60 base pairs (bp) from the transcription start sites of highly active housekeeping genes. ELFs also bound constitutively active, but not poised, macrophage-specific enhancers and promoters. The role of ELFs in promoting high-level constitutive transcription was suggested by multiple evidence: ELF sites enabled robust transcriptional activation by endogenous and minimal synthetic promoters, ELF recruitment was stabilized by the transcriptional machinery, and ELF proteins mediated recruitment of transcriptional and chromatin regulators to core promoters. These data suggest that the co-optation of a limited number of highly active transcription factors represents a broadly adopted strategy to equip both cell type-specific and housekeeping cis-regulatory elements with the ability to efficiently promote transcription.
机译:控制末端分化细胞转录输出的增强子和启动子包括细胞类型特异性和广泛活性的管家元件。这两组顺式调节元件的高本构活性是依赖于完全不同还是依赖于共享的调节剂尚不清楚。通过解剖巨噬细胞的顺式调节谱,我们发现ETS蛋白的ELF亚家族选择性地结合到高活性管家基因转录起始位点的60个碱基对(bp)之内。 ELF还结合组成型活性但不平衡的巨噬细胞特异性增强子和启动子。多种证据表明了ELF在促进高水平组成型转录中的作用:ELF位点可通过内源和最小的合成启动子实现强大的转录激活,ELF募集通过转录机制得以稳定,ELF蛋白介导的转录和染色质调节剂募集到核心推动者。这些数据表明,有限数量的高活性转录因子的共同选择代表了一种广泛采用的策略,该策略可以使细胞类型特异性和内源性顺式调控元件均具有有效促进转录的能力。

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