Aging-associated SATB1 deficiency remodels 3D genome architecture and transcriptional programs in naive CD4 ⁺ T cells
- 1Shanghai Institute of Precision Medicine, Ninth People’s Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200125, China.
- 2Shanghai Key Laboratory of Reproductive Medicine, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Abstract
Precise three-dimensional (3D) genome organization is crucial for regulating gene expression during development, yet its role in age-related transcriptional changes and physiological decline remains elusive. Here, we show that aging reshapes chromatin architecture and gene regulation in murine naive CD4 + T cells, a quiescent T cell population essential for adaptive immunity. Aged naive CD4 + T cells exhibit intrinsic transcriptional reprogramming marked by increased expression of inflammatory and T cell activation–related genes, rendering them more prone to activation. Intriguingly, these changes are accompanied by pronounced alterations in 3D genome organization, including widespread weakening of topologically associating domain (TAD) boundaries and extensive enhancer-promoter rewiring. Mechanistically, we demonstrate that these age-associated structural changes can be partly attributed to the diminished expression of chromatin organizer SATB1. SATB1 colocalizes with CCCTC-binding factor (CTCF) in young naive T cells to spatially constrain CTCF-binding sites. Its decline with age extends the range of CTCF-mediated interactions without altering CTCF occupancy, leading to remodeling of chromatin architecture and up-regulation of proinflammatory and proactivation genes. Conditional SATB1 deletion in naive T cells recapitulates the 3D genome and transcriptional changes observed in aging. Our findings reveal a critical role for SATB1 in maintaining 3D genome integrity in naive T cells and suggest that the dysregulation of genome architecture contributes to immune and organismal aging.
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BibTeX
@article{wang2026agingassociated,
title = {{Aging-associated SATB1 deficiency remodels 3D genome architecture and transcriptional programs in naive CD4 ⁺ T cells}},
author = {Bao Wang and Luzhang Ji and Qian Bian},
journal = {Science Advances},
year = {2026},
month = oct,
doi = {10.1126/sciadv.aeg1622},
url = {https://www.science.org/doi/10.1126/sciadv.aeg1622},
note = {CC BY-NC},
}
RIS
TY - JOUR
TI - Aging-associated SATB1 deficiency remodels 3D genome architecture and transcriptional programs in naive CD4 ⁺ T cells
AU - Bao Wang
AU - Luzhang Ji
AU - Qian Bian
PY - 2026
DA - 2026/10/02
JO - Science Advances
DO - 10.1126/sciadv.aeg1622
UR - https://www.science.org/doi/10.1126/sciadv.aeg1622
AB - Precise three-dimensional (3D) genome organization is crucial for regulating gene expression during development, yet its role in age-related transcriptional changes and physiological decline remains elusive. Here, we show that aging reshapes chromatin architecture and gene regulation in murine naive CD4 + T cells, a quiescent T cell population essential for adaptive immunity. Aged naive CD4 + T cells exhibit intrinsic transcriptional reprogramming marked by increased expression of inflammatory and T cell activation–related genes, rendering them more prone to activation. Intriguingly, these changes are accompanied by pronounced alterations in 3D genome organization, including widespread weakening of topologically associating domain (TAD) boundaries and extensive enhancer-promoter rewiring. Mechanistically, we demonstrate that these age-associated structural changes can be partly attributed to the diminished expression of chromatin organizer SATB1. SATB1 colocalizes with CCCTC-binding factor (CTCF) in young naive T cells to spatially constrain CTCF-binding sites. Its decline with age extends the range of CTCF-mediated interactions without altering CTCF occupancy, leading to remodeling of chromatin architecture and up-regulation of proinflammatory and proactivation genes. Conditional SATB1 deletion in naive T cells recapitulates the 3D genome and transcriptional changes observed in aging. Our findings reveal a critical role for SATB1 in maintaining 3D genome integrity in naive T cells and suggest that the dysregulation of genome architecture contributes to immune and organismal aging.
SN - 2375-2548
ER -