Genetic and Epigenetic Interplay Within a COLGALT2 Enhancer Associated With Osteoarthritis.


Journal

Arthritis & rheumatology (Hoboken, N.J.)
ISSN: 2326-5205
Titre abrégé: Arthritis Rheumatol
Pays: United States
ID NLM: 101623795

Informations de publication

Date de publication:
10 2021
Historique:
received: 30 11 2020
accepted: 11 03 2021
pubmed: 25 3 2021
medline: 10 11 2021
entrez: 24 3 2021
Statut: ppublish

Résumé

The osteoarthritis (OA)-associated single-nucleotide polymorphism (SNP) rs11583641 is located in COLGALT2, encoding a posttranslational modifier of collagen. In cartilage, the SNP genotype correlates with DNA methylation in a putative enhancer. This study was undertaken to characterize the mechanistic relationship between rs11583641, the putative enhancer, and COLGALT2 expression using cartilage samples from human patients and a chondrocyte cell model. Nucleic acids were extracted from articular cartilage samples obtained from patients with OA (n = 137). Samples were genotyped, and DNA methylation was quantified at 12 CpGs using pyrosequencing. The putative enhancer was deleted in Tc28a2 chondrocytes using clustered regularly interspaced short palindromic repeat/Cas9, and the impact on nearby gene expression was determined using real-time quantitative polymerase chain reaction. Targeted modulation of the epigenome using catalytically dead Cas9 (dCas9) constructs fused to DNA methyltransferase 3a or ten-eleven translocase 1 allowed for the investigation of a causal relationship between DNA methylation and enhancer activity. The genotype at rs11583641 correlated with DNA methylation at 3 CpGs, and the presence of the OA risk allele, C, corresponded to reduced levels of methylation. Deletion of the enhancer resulted in a 2.7-fold reduction in COLGALT2 expression. Targeted methylation and demethylation of the CpGs had antagonistic effects on COLGALT2 expression. An allelic imbalance in the expression of COLGALT2 was identified in the cartilage from patients with OA, with relative overexpression of the OA risk allele. Allelic expression ratios correlated with DNA methylation at 4 CpGs. COLGALT2 is a target of OA genetic risk at this locus. The genotype at rs11583641 impacts DNA methylation in a gene enhancer, which, in turn, modulates COLGALT2 expression. COLGALT2 encodes an enzyme that initiates posttranslational glycosylation of collagens and is therefore a compelling OA susceptibility target.

Identifiants

pubmed: 33760386
doi: 10.1002/art.41738
doi:

Substances chimiques

DNMT3A protein, human 0
DNA Methyltransferase 3A EC 2.1.1.37
COLGALT2 protein, human EC 2.4.1.-
Galactosyltransferases EC 2.4.1.-

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1856-1865

Subventions

Organisme : Versus Arthritis
ID : 20771
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/P020941/1
Pays : United Kingdom
Organisme : Seventh Framework Programme
ID : 305815
Organisme : Medical Research Council and Arthritis Research UK as part of the MRC-Arthritis Research UK Centre for Integrated Research into Musculoskeletal Ageing (CIMA)
ID : JXR 10641

Informations de copyright

© 2021 The Authors. Arthritis & Rheumatology published by Wiley Periodicals LLC on behalf of American College of Rheumatology.

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Auteurs

Yulia S Kehayova (YS)

International Centre for Life and Newcastle University, Newcastle-upon-Tyne, UK, and MRC-Arthritis Research UK Centre for Integrated research into Musculoskeletal Ageing and University of Liverpool, Liverpool, UK.

Emily Watson (E)

International Centre for Life and Newcastle University, Newcastle-upon-Tyne, UK, and MRC-Arthritis Research UK Centre for Integrated research into Musculoskeletal Ageing and University of Liverpool, Liverpool, UK.

J Mark Wilkinson (JM)

University of Sheffield, Sheffield, UK, and MRC-Arthritis Research UK Centre for Integrated research into Musculoskeletal Ageing and University of Liverpool, Liverpool, UK.

John Loughlin (J)

International Centre for Life and Newcastle University, Newcastle-upon-Tyne, UK, and MRC-Arthritis Research UK Centre for Integrated research into Musculoskeletal Ageing and University of Liverpool, Liverpool, UK.

Sarah J Rice (SJ)

International Centre for Life and Newcastle University, Newcastle-upon-Tyne, UK, and MRC-Arthritis Research UK Centre for Integrated research into Musculoskeletal Ageing and University of Liverpool, Liverpool, UK.

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