TRIM28 is an essential regulator of three-dimensional chromatin state underpinning CD8+ T cell activation

Abstract T cell activation is accompanied by extensive changes in epigenome. However, the high-ordered chromatin organization underpinning CD8+ T cell activation is not fully known. Here, we show extensive changes in the three-dimensional genome during CD8+ T cell activation, associated with changes...

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Main Authors: Kun Wei, Ruifeng Li, Xiaohong Zhao, Bowen Xie, Tian Xie, Qinli Sun, Yongzhen Chen, Peng Wei, Wei Xu, Xinyi Guo, Zixuan Zhao, Han Feng, Ling Ni, Chen Dong
Format: Article
Language:English
Published: Nature Portfolio 2025-01-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-025-56029-z
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author Kun Wei
Ruifeng Li
Xiaohong Zhao
Bowen Xie
Tian Xie
Qinli Sun
Yongzhen Chen
Peng Wei
Wei Xu
Xinyi Guo
Zixuan Zhao
Han Feng
Ling Ni
Chen Dong
author_facet Kun Wei
Ruifeng Li
Xiaohong Zhao
Bowen Xie
Tian Xie
Qinli Sun
Yongzhen Chen
Peng Wei
Wei Xu
Xinyi Guo
Zixuan Zhao
Han Feng
Ling Ni
Chen Dong
author_sort Kun Wei
collection DOAJ
description Abstract T cell activation is accompanied by extensive changes in epigenome. However, the high-ordered chromatin organization underpinning CD8+ T cell activation is not fully known. Here, we show extensive changes in the three-dimensional genome during CD8+ T cell activation, associated with changes in gene transcription. We show that CD8+ T-cell-specific deletion of Trim28 in mice disrupts autocrine IL-2 production and leads to impaired CD8+ T cell activation in vitro and in vivo. Mechanistically, TRIM28 binds to regulatory regions of genes associated with the formation of chromosomal loops during activation. At the loop anchor regions, TRIM28-occupancy overlaps with that of CTCF, a factor known for defining the boundaries of topologically associating domains and for forming of the loop anchors. In the absence of Trim28, RNA Pol II and cohesin binding to these regions diminishes, and the chromosomal structure required for the active state is disrupted. These results thus identify a critical role for TRIM28-dependent chromatin topology in gene transcription in activated CD8+ T cells.
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institution Kabale University
issn 2041-1723
language English
publishDate 2025-01-01
publisher Nature Portfolio
record_format Article
series Nature Communications
spelling doaj-art-8bbd57bee2e0403dba14abfd63df32912025-01-19T12:31:08ZengNature PortfolioNature Communications2041-17232025-01-0116112010.1038/s41467-025-56029-zTRIM28 is an essential regulator of three-dimensional chromatin state underpinning CD8+ T cell activationKun Wei0Ruifeng Li1Xiaohong Zhao2Bowen Xie3Tian Xie4Qinli Sun5Yongzhen Chen6Peng Wei7Wei Xu8Xinyi Guo9Zixuan Zhao10Han Feng11Ling Ni12Chen Dong13Institute for Immunology, Tsinghua UniversityInstitute for Immunology, Tsinghua UniversityInstitute for Immunology, Tsinghua UniversityInstitute for Immunology, Tsinghua UniversityInstitute for Immunology, Tsinghua UniversityInstitute for Immunology, Tsinghua UniversityInstitute for Immunology, Tsinghua UniversityInstitute for Immunology, Tsinghua UniversityInstitute for Immunology, Tsinghua UniversityInstitute for Immunology, Tsinghua UniversityInstitute for Immunology, Tsinghua UniversityInstitute for Immunology, Tsinghua UniversityInstitute for Immunology, Tsinghua UniversityShanghai Immune Therapy Institute, Shanghai Jiao Tong University School of Medicine- Affiliated Renji HospitalAbstract T cell activation is accompanied by extensive changes in epigenome. However, the high-ordered chromatin organization underpinning CD8+ T cell activation is not fully known. Here, we show extensive changes in the three-dimensional genome during CD8+ T cell activation, associated with changes in gene transcription. We show that CD8+ T-cell-specific deletion of Trim28 in mice disrupts autocrine IL-2 production and leads to impaired CD8+ T cell activation in vitro and in vivo. Mechanistically, TRIM28 binds to regulatory regions of genes associated with the formation of chromosomal loops during activation. At the loop anchor regions, TRIM28-occupancy overlaps with that of CTCF, a factor known for defining the boundaries of topologically associating domains and for forming of the loop anchors. In the absence of Trim28, RNA Pol II and cohesin binding to these regions diminishes, and the chromosomal structure required for the active state is disrupted. These results thus identify a critical role for TRIM28-dependent chromatin topology in gene transcription in activated CD8+ T cells.https://doi.org/10.1038/s41467-025-56029-z
spellingShingle Kun Wei
Ruifeng Li
Xiaohong Zhao
Bowen Xie
Tian Xie
Qinli Sun
Yongzhen Chen
Peng Wei
Wei Xu
Xinyi Guo
Zixuan Zhao
Han Feng
Ling Ni
Chen Dong
TRIM28 is an essential regulator of three-dimensional chromatin state underpinning CD8+ T cell activation
Nature Communications
title TRIM28 is an essential regulator of three-dimensional chromatin state underpinning CD8+ T cell activation
title_full TRIM28 is an essential regulator of three-dimensional chromatin state underpinning CD8+ T cell activation
title_fullStr TRIM28 is an essential regulator of three-dimensional chromatin state underpinning CD8+ T cell activation
title_full_unstemmed TRIM28 is an essential regulator of three-dimensional chromatin state underpinning CD8+ T cell activation
title_short TRIM28 is an essential regulator of three-dimensional chromatin state underpinning CD8+ T cell activation
title_sort trim28 is an essential regulator of three dimensional chromatin state underpinning cd8 t cell activation
url https://doi.org/10.1038/s41467-025-56029-z
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