bioRxivMolecular BiologyPreprint
SUMOylation differentially regulates SMCHD1 complex formation and function in a genomic context-specific manner
Remko GoossensiD, Mara S. TihayaiD, Iris M. WillemseniD, Kirsten R. Straasheijm, Patrick J. van der VlietiD, Román González‐PrietoiD, Alfred C.O. VertegaaliD, Stephen J. TapscottiD, Judit BalogiD, Silvère M. van der MaareliD
Abstract
Structural Maintenance of Chromosomes Hinge Domain Containing 1 (SMCHD1) is a chromatin repressor regulating gene expression and chromatin architecture of distinct autosomal and X-chromosomal loci. SMCHD1 mutations cause derepression of the D4Z4 macrosatellite repeat-embedded DUX4 gene in skeletal muscle of facioscapulohumeral muscular dystrophy (FSHD) patients Little is known about the regulation and post-translational modification of SMCHD1. Here we report the SUMOylation dynamics of SMCHD1 and its impact on autosomal single copy and repetitive loci, and the inactive X chromosome (Xi). We identify that SMCHD1 is SUMOylated primarily at lysine 1374, uncover factors regulating SMCHD1 SUMOylation, and demonstrate that SMCHD1 interacts with chromatin repressors TRIM28, HNRNPK and SETDB1 in a SUMO-dependent manner. We find that SUMOylation impacts Xi engagement of SMCHD1, maintenance of a repressive D4Z4 chromatin structure preventing DUX4 expression, and regulation of LRIF1 promoter activity. The rapid, SUMO-dependent upregulation of DUX4 could explain the bursts of DUX4 expression typical for FSHD muscle.
- organism: human
- assay: DNA methylation
- assay: ChIP-seq
- research focus: gene regulatory network inference
- research focus: differential expression
- research focus: variant effect prediction
- approach: statistical model
- approach: experimental assay
- Citations
- 1
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Chemical inhibition of SUMOylation activates the FSHD locus
Alice Nordlinger, Loéva Morin, … Frédérique Magdinier·Scientific ReportsPeer-reviewed·Jan 9, 2026
- Engineered SMCHD1 and D4Z4 mutations reveal roles of D4Z4 heterochromatin disruption and feedforward DUX4 network activation in FSHD
Xiangduo Kong, Nam Viet Nguyen, … Kyoko Yokomori·bioRxiv·Oct 14, 2022
- SMCHD1 loss re-wires MYOD1 enhancer nexuses and chromatin accessibility landscapes in muscle cells
Zhijun Huang, Wei Cui, … Gerd P. Pfeifer·bioRxiv·Feb 22, 2026
- Selective interaction of the protein SMCHD1 with specific chromatin regions is governed by the loading factor LRIF1 and SMCHD1 ATPase activity
Flavia Constantinescu, Aleksander Szczurek, … Neil Brockdorff·bioRxiv·Jun 13, 2025
- SMCHD1 loss triggers DUX4 expression by disrupting splicing in FSHD2
Eden Engal, Aveksha Sharma, … Yotam Drier·Science AdvancesPeer-reviewed·May 29, 2024
- SMCHD1 variants may induce variegated expression in Facio Scapulo Humeral Dystophy and Bosma Arhinia and microphtalmia syndrome
Camille Laberthonnìère, Raphaël Chevalier, … Frédérique Magdinier·bioRxiv·May 17, 2021