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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
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.
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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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