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NF90/ILF3 is a transcription factor that promotes proliferation over differentiation by hierarchical regulation in K562 erythroleukemia cells

机译:NF90 / ILF3是一种转录因子通过K562红白血病细胞中的分级调控促进分化过程中的增殖

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摘要

NF90 and splice variant NF110 are DNA- and RNA-binding proteins encoded by the Interleukin enhancer-binding factor 3 (ILF3) gene that have been established to regulate RNA splicing, stabilization and export. The roles of NF90 and NF110 in regulating transcription as chromatin-interacting proteins have not been comprehensively characterized. Here, chromatin immunoprecipitation followed by deep sequencing (ChIP-seq) identified 9,081 genomic sites specifically occupied by NF90/NF110 in K562 cells. One third of NF90/NF110 peaks occurred at promoters of annotated genes. NF90/NF110 occupancy colocalized with chromatin marks associated with active promoters and strong enhancers. Comparison with 150 ENCODE ChIP-seq experiments revealed that NF90/NF110 clustered with transcription factors exhibiting preference for promoters over enhancers (POLR2A, MYC, YY1). Differential gene expression analysis following shRNA knockdown of NF90/NF110 in K562 cells revealed that NF90/NF110 activates transcription factors that drive growth and proliferation (EGR1, MYC), while attenuating differentiation along the erythroid lineage (KLF1). NF90/NF110 associates with chromatin to hierarchically regulate transcription factors that promote proliferation and suppress differentiation.
机译:NF90和剪接变体NF110是由白介素增强子结合因子3(ILF3)基因编码的DNA和RNA结合蛋白,已被建立来调节RNA剪接,稳定和输出。尚未全面表征NF90和NF110在调节转录中作为染色质相互作用蛋白的作用。在这里,染色质免疫沉淀后再进行深度测序(ChIP-seq),确定了K081细胞中NF90 / NF110特异性占据的9,081个基因组位点。 NF90 / NF110峰的三分之一出现在注释基因的启动子上。 NF90 / NF110占用与染色质标记共定位,而染色质标记与活性启动子和强促进剂相关。与150个ENCODE ChIP-seq实验的比较表明,NF90 / NF110与转录因子聚集在一起,表现出对启动子的偏好高于增强子(POLR2A,MYC,YY1)。 shRNA敲除NF90 / NF110在K562细胞中后的差异基因表达分析表明,NF90 / NF110激活驱动生长和增殖的转录因子(EGR1,MYC),同时减弱沿红系谱系(KLF1)的分化。 NF90 / NF110与染色质结合,以分级调节转录因子,从而促进增殖并抑制分化。

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