Fate erasure logic of gene networks underlying direct neuronal conversion of somatic cells by microRNAs

Summary: Neurogenic microRNAs 9/9∗ and 124 (miR-9/9∗-124) drive the direct reprogramming of human fibroblasts into neurons with the initiation of the fate erasure of fibroblasts. However, whether the miR-9/9∗-124 fate erasure logic extends to the neuronal conversion of other somatic cell types remai...

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Main Authors: Kitra Cates, Luorongxin Yuan, Yan Yang, Andrew S. Yoo
Format: Article
Language:English
Published: Elsevier 2025-01-01
Series:Cell Reports
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Online Access:http://www.sciencedirect.com/science/article/pii/S2211124724015043
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author Kitra Cates
Luorongxin Yuan
Yan Yang
Andrew S. Yoo
author_facet Kitra Cates
Luorongxin Yuan
Yan Yang
Andrew S. Yoo
author_sort Kitra Cates
collection DOAJ
description Summary: Neurogenic microRNAs 9/9∗ and 124 (miR-9/9∗-124) drive the direct reprogramming of human fibroblasts into neurons with the initiation of the fate erasure of fibroblasts. However, whether the miR-9/9∗-124 fate erasure logic extends to the neuronal conversion of other somatic cell types remains unknown. Here, we uncover that miR-9/9∗-124 induces neuronal conversion of multiple cell types: dura fibroblasts, astrocytes, smooth muscle cells, and pericytes. We reveal the cell-type-specific and pan-somatic gene network erasure induced by miR-9/9∗-124, including cell cycle, morphology, and proteostasis gene networks. Leveraging these pan-somatic gene networks, we predict upstream regulators that may antagonize somatic fate erasure. Among the predicted regulators, we identify TP53 (p53), whose inhibition is sufficient to enhance neuronal conversion even in post-mitotic cells. This study extends miR-9/9∗-124 reprogramming to alternate somatic cells, reveals the pan-somatic gene network fate erasure logic of miR-9/9∗-124, and shows a neurogenic role for p53 inhibition in the miR-9/9∗-124 signaling cascade.
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spelling doaj-art-9a455d1943ea4a6eafea06b3254df29c2025-01-06T04:08:37ZengElsevierCell Reports2211-12472025-01-01441115153Fate erasure logic of gene networks underlying direct neuronal conversion of somatic cells by microRNAsKitra Cates0Luorongxin Yuan1Yan Yang2Andrew S. Yoo3Department 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 Genetics, Stanford University, Stanford, CA 94305, USADepartment 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, USADepartment of Developmental Biology, Washington University School of Medicine, St. Louis, MO 63110, USADepartment of Developmental Biology, Washington University School of Medicine, St. Louis, MO 63110, USA; Center of Regenerative Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA; Corresponding authorSummary: Neurogenic microRNAs 9/9∗ and 124 (miR-9/9∗-124) drive the direct reprogramming of human fibroblasts into neurons with the initiation of the fate erasure of fibroblasts. However, whether the miR-9/9∗-124 fate erasure logic extends to the neuronal conversion of other somatic cell types remains unknown. Here, we uncover that miR-9/9∗-124 induces neuronal conversion of multiple cell types: dura fibroblasts, astrocytes, smooth muscle cells, and pericytes. We reveal the cell-type-specific and pan-somatic gene network erasure induced by miR-9/9∗-124, including cell cycle, morphology, and proteostasis gene networks. Leveraging these pan-somatic gene networks, we predict upstream regulators that may antagonize somatic fate erasure. Among the predicted regulators, we identify TP53 (p53), whose inhibition is sufficient to enhance neuronal conversion even in post-mitotic cells. This study extends miR-9/9∗-124 reprogramming to alternate somatic cells, reveals the pan-somatic gene network fate erasure logic of miR-9/9∗-124, and shows a neurogenic role for p53 inhibition in the miR-9/9∗-124 signaling cascade.http://www.sciencedirect.com/science/article/pii/S2211124724015043CP: Stem cell researchCP: Molecular biology
spellingShingle Kitra Cates
Luorongxin Yuan
Yan Yang
Andrew S. Yoo
Fate erasure logic of gene networks underlying direct neuronal conversion of somatic cells by microRNAs
Cell Reports
CP: Stem cell research
CP: Molecular biology
title Fate erasure logic of gene networks underlying direct neuronal conversion of somatic cells by microRNAs
title_full Fate erasure logic of gene networks underlying direct neuronal conversion of somatic cells by microRNAs
title_fullStr Fate erasure logic of gene networks underlying direct neuronal conversion of somatic cells by microRNAs
title_full_unstemmed Fate erasure logic of gene networks underlying direct neuronal conversion of somatic cells by microRNAs
title_short Fate erasure logic of gene networks underlying direct neuronal conversion of somatic cells by microRNAs
title_sort fate erasure logic of gene networks underlying direct neuronal conversion of somatic cells by micrornas
topic CP: Stem cell research
CP: Molecular biology
url http://www.sciencedirect.com/science/article/pii/S2211124724015043
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AT luorongxinyuan fateerasurelogicofgenenetworksunderlyingdirectneuronalconversionofsomaticcellsbymicrornas
AT yanyang fateerasurelogicofgenenetworksunderlyingdirectneuronalconversionofsomaticcellsbymicrornas
AT andrewsyoo fateerasurelogicofgenenetworksunderlyingdirectneuronalconversionofsomaticcellsbymicrornas