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首页> 外文期刊>Nucleic Acids Research >Pre-B cell to macrophage transdifferentiation without significant promoter DNA methylation changes
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Pre-B cell to macrophage transdifferentiation without significant promoter DNA methylation changes

机译:从前B细胞到巨噬细胞的转分化而没有明显的启动子DNA甲基化变化

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Transcription factor-induced lineage reprogramming or transdifferentiation experiments are essential for understanding the plasticity of differentiated cells. These experiments helped to define the specific role of transcription factors in conferring cell identity and played a key role in the development of the regenerative medicine field. We here investigated the acquisition of DNA methylation changes during C/EBP alpha-induced pre-B cell to macrophage transdifferentiation. Unexpectedly, cell lineage conversion occurred without significant changes in DNA methylation not only in key B cell- and macrophage-specific genes but also throughout the entire set of genes differentially methylated between the two parental cell types. In contrast, active and repressive histone modification marks changed according to the expression levels of these genes. We also demonstrated that C/EBP alpha and RNA Pol II are associated with the methylated promoters of macrophage-specific genes in reprogrammed macrophages without inducing methylation changes. Our findings not only provide insights about the extent and hierarchy of epigenetic events in pre-B cell to macrophage transdifferentiation but also show an important difference to reprogramming towards pluripotency where promoter DNA demethylation plays a pivotal role.
机译:转录因子诱导的谱系重编程或转分化实验对于理解分化细胞的可塑性至关重要。这些实验帮助确定了转录因子在赋予细胞身份方面的特定作用,并在再生医学领域的发展中发挥了关键作用。我们在这里调查了C / EBPα诱导的前B细胞向巨噬细胞转分化过程中DNA甲基化变化的获取。出乎意料的是,不仅在关键的B细胞和巨噬细胞特异性基因中,而且在两种亲代细胞类型之间甲基化差异化的整个基因中,细胞谱系转换都没有显着改变DNA甲基化。相反,活性和抑制性组蛋白修饰标记根据这些基因的表达水平而改变。我们还证明,C / EBPα和RNA Pol II与重新编程的巨噬细胞中巨噬细胞特异性基因的甲基化启动子相关,而不会引起甲基化变化。我们的发现不仅提供了关于前B细胞到巨噬细胞转分化中表观遗传事件的程度和层次的见解,而且还显示了重编程向多能性的重要差异,在多能性中启动子DNA去甲基化起着关键作用。

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