Department of Developmental Biology, Washington University School of Medicine, St. Louis, MO 63110, USA; Program in Molecular Genetics and Genomics, Washington University School of Medicine, St. Louis, MO 63110, USA.
Department of Developmental Biology, Washington University School of Medicine, St. Louis, MO 63110, USA; Program in Computational and Systems Biology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Cell Stem Cell. 2021 Jan 7;28(1):127-140.e9. doi: 10.1016/j.stem.2020.08.015. Epub 2020 Sep 21.
Cell-fate conversion generally requires reprogramming effectors to both introduce fate programs of the target cell type and erase the identity of starting cell population. Here, we reveal insights into the activity of microRNAs miR-9/9 and miR-124 (miR-9/9-124) as reprogramming agents that orchestrate direct conversion of human fibroblasts into motor neurons by first eradicating fibroblast identity and promoting uniform transition to a neuronal state in sequence. We identify KLF-family transcription factors as direct target genes for miR-9/9-124 and show their repression is critical for erasing fibroblast fate. Subsequent gain of neuronal identity requires upregulation of a small nuclear RNA, RN7SK, which induces accessibilities of chromatin regions and neuronal gene activation to push cells to a neuronal state. Our study defines deterministic components in the microRNA-mediated reprogramming cascade.
细胞命运转变通常需要重新编程效应器,既要引入目标细胞类型的命运程序,又要抹去起始细胞群体的身份。在这里,我们揭示了 microRNAs miR-9/9 和 miR-124(miR-9/9-124)作为重编程剂的作用机制,这些 microRNAs 可以通过首先消除成纤维细胞的身份,并依次促进向神经元状态的均匀转变,协调将人成纤维细胞直接转化为运动神经元。我们确定 KLF 家族转录因子是 miR-9/9-124 的直接靶基因,并表明它们的抑制对于消除成纤维细胞命运至关重要。随后获得神经元身份需要上调小核 RNA RN7SK,它诱导染色质区域的可及性和神经元基因激活,将细胞推向神经元状态。我们的研究定义了 microRNA 介导的重编程级联中的确定性成分。