SMCHD1 loss rewires MYOD1 enhancer nexuses and chromatin accessibility landscapes in muscle cells
- 1Department of Epigenetics, Van Andel Institute, Grand Rapids, MI, USA.
Abstract
SMCHD1 is a chromatin architectural protein linked to heterochromatin repression. Loss of function mutations of SMCHD1 cause facioscapulohumeral muscular dystrophy type 2 (FSHD2) through activation of the DUX4 transcription factor gene. However, it is unknown how SMCHD1 may regulate transcription independently of DUX4. Here, we show that SMCHD1 safeguards enhancer organization within the three-dimensional (3D) genome in human myoblasts. Loss of SMCHD1 leads to widespread gains in chromatin accessibility, aberrant transcription, and selective remodeling of myogenic transcription factor MYOD1 occupancy. Integrative analyses of histone modifications, chromatin accessibility, Hi-C looping, and enhancer-gene modeling reveal that SMCHD1 loss rewires the landscape of clustered enhancers and promotes the emergence of new networks of enhancer elements, termed MYOD1 enhancer nexuses. These structures are marked by increased enhancer connectivity, increased local 3D chromatin interactions, and coordinated activation of genes likely relevant for FSHD pathology. Our findings identify SMCHD1 as a key architectural constraint that suppresses hyperactive enhancer networks, thereby preserving transcriptional homeostasis in myoblasts.
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BibTeX
@article{huang2026smchd1,
title = {{SMCHD1 loss rewires MYOD1 enhancer nexuses and chromatin accessibility landscapes in muscle cells}},
author = {Zhijun Huang and Wei Cui and Adam Klaiss and Gerd P. Pfeifer},
journal = {Science Advances},
year = {2026},
month = oct,
doi = {10.1126/sciadv.aeh7499},
url = {https://www.science.org/doi/10.1126/sciadv.aeh7499},
note = {CC BY-NC},
}
RIS
TY - JOUR
TI - SMCHD1 loss rewires MYOD1 enhancer nexuses and chromatin accessibility landscapes in muscle cells
AU - Zhijun Huang
AU - Wei Cui
AU - Adam Klaiss
AU - Gerd P. Pfeifer
PY - 2026
DA - 2026/10/23
JO - Science Advances
DO - 10.1126/sciadv.aeh7499
UR - https://www.science.org/doi/10.1126/sciadv.aeh7499
AB - SMCHD1 is a chromatin architectural protein linked to heterochromatin repression. Loss of function mutations of SMCHD1 cause facioscapulohumeral muscular dystrophy type 2 (FSHD2) through activation of the DUX4 transcription factor gene. However, it is unknown how SMCHD1 may regulate transcription independently of DUX4. Here, we show that SMCHD1 safeguards enhancer organization within the three-dimensional (3D) genome in human myoblasts. Loss of SMCHD1 leads to widespread gains in chromatin accessibility, aberrant transcription, and selective remodeling of myogenic transcription factor MYOD1 occupancy. Integrative analyses of histone modifications, chromatin accessibility, Hi-C looping, and enhancer-gene modeling reveal that SMCHD1 loss rewires the landscape of clustered enhancers and promotes the emergence of new networks of enhancer elements, termed MYOD1 enhancer nexuses. These structures are marked by increased enhancer connectivity, increased local 3D chromatin interactions, and coordinated activation of genes likely relevant for FSHD pathology. Our findings identify SMCHD1 as a key architectural constraint that suppresses hyperactive enhancer networks, thereby preserving transcriptional homeostasis in myoblasts.
SN - 2375-2548
ER -