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Dynamic change of transcription pausing through modulating NELF protein stability regulates granulocytic differentiation

机译:通过调节NELF蛋白的稳定性转录暂停的动态变化可调节粒细胞的分化

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摘要

The negative elongation factor (NELF) complex is a metazoan-specific factor essential for establishing transcription pausing. Although NELF has been implicated in cell-fate regulation, the cellular regulation of NELF and its intrinsic role in specific lineage differentiation remains largely unknown. Using mammalian hematopoietic differentiation as a model system, here we identified a dynamic change of NELF-mediated transcription pausing as a novel mechanism regulating hematopoietic differentiation. We found a sharp decrease of NELF protein abundance upon granulocytic differentiation and a subsequent genome-wide reduction of transcription pausing. This loss of pausing coincides with activation of granulocyte-affiliated genes and diminished expression of progenitor markers. Functional studies revealed that sustained expression of NELF inhibits granulocytic differentiation, whereas NELF depletion in progenitor cells leads to premature differentiation toward the granulocytic lineage. Our results thus uncover a previously unrecognized regulation of transcription pausing by modulating NELF protein abundance to control cellular differentiation.
机译:负伸长因子(NELF)复合物是后生动物特异性因子,对于建立转录暂停至关重要。尽管NELF与细胞命运调控有关,但是NELF的细胞调控及其在特定谱系分化中的内在作用仍然未知。使用哺乳动物的造血分化为模型系统,在这里我们确定了动态改变的NELF介导的转录暂停作为调节造血分化的新机制。我们发现粒细胞分化后NELF蛋白丰度急剧下降,随后全基因组转录暂停减少。停顿的丧失与粒细胞相关基因的激活和祖细胞标记的表达减少同时发生。功能研究表明,NELF的持续表达抑制了粒细胞的分化,而祖细胞中NELF的耗尽导致向粒细胞谱系的过早分化。因此,我们的结果揭示了通过调节NELF蛋白丰度来控制细胞分化,从而实现了转录暂停的未知功能。

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