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CTCF-mediated chromatin looping in EGR2 regulation and SUZ12 recruitment critical for peripheral myelination and repair
Chromatin organization is critical for cell growth, differentiation, and disease development, however, its functions in peripheral myelination and myelin repair remain elusive. In this report, we demonstrate that the CCCTC-binding factor (CTCF), a crucial chromatin organizer, is essential for Schwan...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7431862/ https://www.ncbi.nlm.nih.gov/pubmed/32807777 http://dx.doi.org/10.1038/s41467-020-17955-2 |
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author | Wang, Jincheng Wang, Jiajia Yang, Lijun Zhao, Chuntao Wu, Laiman Natalie Xu, Lingli Zhang, Feng Weng, Qinjie Wegner, Michael Lu, Q. Richard |
author_facet | Wang, Jincheng Wang, Jiajia Yang, Lijun Zhao, Chuntao Wu, Laiman Natalie Xu, Lingli Zhang, Feng Weng, Qinjie Wegner, Michael Lu, Q. Richard |
author_sort | Wang, Jincheng |
collection | PubMed |
description | Chromatin organization is critical for cell growth, differentiation, and disease development, however, its functions in peripheral myelination and myelin repair remain elusive. In this report, we demonstrate that the CCCTC-binding factor (CTCF), a crucial chromatin organizer, is essential for Schwann cell myelination and myelin regeneration after nerve injury. Inhibition of CTCF or its deletion blocks Schwann cell differentiation at the pro-myelinating stage, whereas overexpression of CTCF promotes the myelination program. We find that CTCF establishes chromatin interaction loops between enhancer and promoter regulatory elements and promotes expression of a key pro-myelinogenic factor EGR2. In addition, CTCF interacts with SUZ12, a component of polycomb-repressive-complex 2 (PRC2), to repress the transcriptional program associated with negative regulation of Schwann cell maturation. Together, our findings reveal a dual role of CTCF-dependent chromatin organization in promoting myelinogenic programs and recruiting chromatin-repressive complexes to block Schwann cell differentiation inhibitors to control peripheral myelination and repair. |
format | Online Article Text |
id | pubmed-7431862 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74318622020-08-28 CTCF-mediated chromatin looping in EGR2 regulation and SUZ12 recruitment critical for peripheral myelination and repair Wang, Jincheng Wang, Jiajia Yang, Lijun Zhao, Chuntao Wu, Laiman Natalie Xu, Lingli Zhang, Feng Weng, Qinjie Wegner, Michael Lu, Q. Richard Nat Commun Article Chromatin organization is critical for cell growth, differentiation, and disease development, however, its functions in peripheral myelination and myelin repair remain elusive. In this report, we demonstrate that the CCCTC-binding factor (CTCF), a crucial chromatin organizer, is essential for Schwann cell myelination and myelin regeneration after nerve injury. Inhibition of CTCF or its deletion blocks Schwann cell differentiation at the pro-myelinating stage, whereas overexpression of CTCF promotes the myelination program. We find that CTCF establishes chromatin interaction loops between enhancer and promoter regulatory elements and promotes expression of a key pro-myelinogenic factor EGR2. In addition, CTCF interacts with SUZ12, a component of polycomb-repressive-complex 2 (PRC2), to repress the transcriptional program associated with negative regulation of Schwann cell maturation. Together, our findings reveal a dual role of CTCF-dependent chromatin organization in promoting myelinogenic programs and recruiting chromatin-repressive complexes to block Schwann cell differentiation inhibitors to control peripheral myelination and repair. Nature Publishing Group UK 2020-08-17 /pmc/articles/PMC7431862/ /pubmed/32807777 http://dx.doi.org/10.1038/s41467-020-17955-2 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Wang, Jincheng Wang, Jiajia Yang, Lijun Zhao, Chuntao Wu, Laiman Natalie Xu, Lingli Zhang, Feng Weng, Qinjie Wegner, Michael Lu, Q. Richard CTCF-mediated chromatin looping in EGR2 regulation and SUZ12 recruitment critical for peripheral myelination and repair |
title | CTCF-mediated chromatin looping in EGR2 regulation and SUZ12 recruitment critical for peripheral myelination and repair |
title_full | CTCF-mediated chromatin looping in EGR2 regulation and SUZ12 recruitment critical for peripheral myelination and repair |
title_fullStr | CTCF-mediated chromatin looping in EGR2 regulation and SUZ12 recruitment critical for peripheral myelination and repair |
title_full_unstemmed | CTCF-mediated chromatin looping in EGR2 regulation and SUZ12 recruitment critical for peripheral myelination and repair |
title_short | CTCF-mediated chromatin looping in EGR2 regulation and SUZ12 recruitment critical for peripheral myelination and repair |
title_sort | ctcf-mediated chromatin looping in egr2 regulation and suz12 recruitment critical for peripheral myelination and repair |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7431862/ https://www.ncbi.nlm.nih.gov/pubmed/32807777 http://dx.doi.org/10.1038/s41467-020-17955-2 |
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