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PRC2 Acts as a Critical Timer That Drives Oligodendrocyte Fate over Astrocyte Identity by Repressing the Notch Pathway
PRC2 creates the repressive mark histone H3 Lys27 trimethylation. Although PRC2 is involved in various biological processes, its role in glial development remains ambiguous. Here, we show that PRC2 is required for oligodendrocyte (OL) differentiation and myelination, but not for OL precursor formati...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8070886/ https://www.ncbi.nlm.nih.gov/pubmed/32937136 http://dx.doi.org/10.1016/j.celrep.2020.108147 |
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author | Wang, Wenxian Cho, Hyeyoung Kim, Dongkyeong Park, Younjung Moon, Ji Hwan Lim, Su Jeong Yoon, Sung Min McCane, Michael Aicher, Sue A. Kim, Sangsoo Emery, Ben Lee, Jae W. Lee, Seunghee Park, Yungki Lee, Soo-Kyung |
author_facet | Wang, Wenxian Cho, Hyeyoung Kim, Dongkyeong Park, Younjung Moon, Ji Hwan Lim, Su Jeong Yoon, Sung Min McCane, Michael Aicher, Sue A. Kim, Sangsoo Emery, Ben Lee, Jae W. Lee, Seunghee Park, Yungki Lee, Soo-Kyung |
author_sort | Wang, Wenxian |
collection | PubMed |
description | PRC2 creates the repressive mark histone H3 Lys27 trimethylation. Although PRC2 is involved in various biological processes, its role in glial development remains ambiguous. Here, we show that PRC2 is required for oligodendrocyte (OL) differentiation and myelination, but not for OL precursor formation. PRC2-deficient OL lineage cells differentiate into OL precursors, but they fail to trigger the molecular program for myelination, highlighting that PRC2 is essential for directing the differentiation timing of OL precursors. PRC2 null OL lineage cells aberrantly induce Notch pathway genes and acquire astrocytic features. The repression of the Notch pathway restores the myelination program and inhibits abnormal astrocytic differentiation in the PRC2-deficient OL lineage, indicating that Notch is a major target of PRC2. Altogether, our studies propose a specific action of PRC2 as a novel gatekeeper that determines the glial fate choice and the timing of OL lineage progression and myelination by impinging on the Notch pathway. |
format | Online Article Text |
id | pubmed-8070886 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
record_format | MEDLINE/PubMed |
spelling | pubmed-80708862021-04-25 PRC2 Acts as a Critical Timer That Drives Oligodendrocyte Fate over Astrocyte Identity by Repressing the Notch Pathway Wang, Wenxian Cho, Hyeyoung Kim, Dongkyeong Park, Younjung Moon, Ji Hwan Lim, Su Jeong Yoon, Sung Min McCane, Michael Aicher, Sue A. Kim, Sangsoo Emery, Ben Lee, Jae W. Lee, Seunghee Park, Yungki Lee, Soo-Kyung Cell Rep Article PRC2 creates the repressive mark histone H3 Lys27 trimethylation. Although PRC2 is involved in various biological processes, its role in glial development remains ambiguous. Here, we show that PRC2 is required for oligodendrocyte (OL) differentiation and myelination, but not for OL precursor formation. PRC2-deficient OL lineage cells differentiate into OL precursors, but they fail to trigger the molecular program for myelination, highlighting that PRC2 is essential for directing the differentiation timing of OL precursors. PRC2 null OL lineage cells aberrantly induce Notch pathway genes and acquire astrocytic features. The repression of the Notch pathway restores the myelination program and inhibits abnormal astrocytic differentiation in the PRC2-deficient OL lineage, indicating that Notch is a major target of PRC2. Altogether, our studies propose a specific action of PRC2 as a novel gatekeeper that determines the glial fate choice and the timing of OL lineage progression and myelination by impinging on the Notch pathway. 2020-09-15 /pmc/articles/PMC8070886/ /pubmed/32937136 http://dx.doi.org/10.1016/j.celrep.2020.108147 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ). |
spellingShingle | Article Wang, Wenxian Cho, Hyeyoung Kim, Dongkyeong Park, Younjung Moon, Ji Hwan Lim, Su Jeong Yoon, Sung Min McCane, Michael Aicher, Sue A. Kim, Sangsoo Emery, Ben Lee, Jae W. Lee, Seunghee Park, Yungki Lee, Soo-Kyung PRC2 Acts as a Critical Timer That Drives Oligodendrocyte Fate over Astrocyte Identity by Repressing the Notch Pathway |
title | PRC2 Acts as a Critical Timer That Drives Oligodendrocyte Fate over Astrocyte Identity by Repressing the Notch Pathway |
title_full | PRC2 Acts as a Critical Timer That Drives Oligodendrocyte Fate over Astrocyte Identity by Repressing the Notch Pathway |
title_fullStr | PRC2 Acts as a Critical Timer That Drives Oligodendrocyte Fate over Astrocyte Identity by Repressing the Notch Pathway |
title_full_unstemmed | PRC2 Acts as a Critical Timer That Drives Oligodendrocyte Fate over Astrocyte Identity by Repressing the Notch Pathway |
title_short | PRC2 Acts as a Critical Timer That Drives Oligodendrocyte Fate over Astrocyte Identity by Repressing the Notch Pathway |
title_sort | prc2 acts as a critical timer that drives oligodendrocyte fate over astrocyte identity by repressing the notch pathway |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8070886/ https://www.ncbi.nlm.nih.gov/pubmed/32937136 http://dx.doi.org/10.1016/j.celrep.2020.108147 |
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