Selective interaction of SMCHD1 with chromatin is governed by LRIF1 and SMCHD1 ATPase activity

The chromosomal protein SMCHD1 is a GHKL ATPase with important roles in epigenetic silencing, including on the inactive X chromosome (Xi). Mutations of SMCHD1 have been linked to facioscapulohumeral muscular dystrophy (FSHD) and Bosma arrhinia microphthalmia syndrome (BAMS). Here, we use live-cell and single-molecule imaging to investigate SMCHD1 interactions with chromatin and its function in epigenetic silencing. We show that chromatin binding of SMCHD1 genome-wide, including on the Xi, is critically dependent on the protein LRIF1 that mediates interaction with H3K9me2/3-modified nucleosomes. Engineered mutations in the GHKL ATPase domain demonstrate that ATP hydrolysis is required for selective enrichment of SMCHD1 at specific chromatin regions, which is critical for X-linked gene silencing. Conversely, gain-of-function BAMS-associated mutations are linked to accelerated Xi recruitment and gene silencing, or increased Xi compaction. Together, our findings advance understanding of SMCHD1 recruitment and function on the Xi and at other target sites in the genome.

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Publication Details

Journal
Nature Communications
Published
2026-06-16
DOI
https://doi.org/10.1038/s41467-026-74427-9
Primary Topic
Muscle Physiology and Disorders
Type
article
Field-Weighted Citation Impact
0.00

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article

Selective interaction of SMCHD1 with chromatin is governed by LRIF1 and SMCHD1 ATPase activity

Guifeng Wei, Jessica R. Kelley, Flavia Constantinescu, Stephan Uphoff et al.
Nature Communications
Muscle Physiology and Disorders
article

Selective interaction of SMCHD1 with chromatin is governed by LRIF1 and SMCHD1 ATPase activity

Guifeng Wei, Jessica R. Kelley, Flavia Constantinescu, Stephan Uphoff, Tatyana B. Nesterova, Adam D. Cawte, Mafalda Almeida, Neil Brockdorff, Victoria Pustygina, Aleksander T. Szczurek
article en

Abstract

The chromosomal protein SMCHD1 is a GHKL ATPase with important roles in epigenetic silencing, including on the inactive X chromosome (Xi). Mutations of SMCHD1 have been linked to facioscapulohumeral muscular dystrophy (FSHD) and Bosma arrhinia microphthalmia syndrome (BAMS). Here, we use live-cell and single-molecule imaging to investigate SMCHD1 interactions with chromatin and its function in epigenetic silencing. We show that chromatin binding of SMCHD1 genome-wide, including on the Xi, is critically dependent on the protein LRIF1 that mediates interaction with H3K9me2/3-modified nucleosomes. Engineered mutations in the GHKL ATPase domain demonstrate that ATP hydrolysis is required for selective enrichment of SMCHD1 at specific chromatin regions, which is critical for X-linked gene silencing. Conversely, gain-of-function BAMS-associated mutations are linked to accelerated Xi recruitment and gene silencing, or increased Xi compaction. Together, our findings advance understanding of SMCHD1 recruitment and function on the Xi and at other target sites in the genome.

Nature Communications
University of Oxford (GB), Science Oxford (GB)
Wellcome, Wellcome Trust, UK Research and Innovation, University of Oxford, Lister Institute of Preventive Medicine, Engineering and Physical Sciences Research Council, Clarendon Fund
Openalex Percentile: Top 12%
Muscle Physiology and Disorders
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