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Methylome and transcriptome profiling in Myasthenia Gravis monozygotic twins
S. Mamrut, N. Avidan, F. Truffault, E. Staun-Ram, T. Sharshar, B. Eymard, M. Frenkian, J. Pitha, M. de Baets, L. Servais, S. Berrih-Aknin, A. Miller,
Language English Country England, Great Britain
Document type Journal Article, Twin Study
- MeSH
- CpG Islands MeSH
- Adult MeSH
- Twins, Monozygotic * MeSH
- Epigenesis, Genetic MeSH
- Genetic Predisposition to Disease MeSH
- Genetic Association Studies MeSH
- Middle Aged MeSH
- Humans MeSH
- DNA Methylation * MeSH
- Young Adult MeSH
- Monocytes immunology metabolism MeSH
- Myasthenia Gravis genetics metabolism MeSH
- Triggering Receptor Expressed on Myeloid Cells-1 genetics metabolism MeSH
- Aged MeSH
- Signal Transduction MeSH
- Gene Expression Profiling MeSH
- Case-Control Studies MeSH
- Transcriptome * MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Young Adult MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Twin Study MeSH
OBJECTIVE: To identify novel genetic and epigenetic factors associated with Myasthenia gravis (MG) using an identical twins experimental study design. METHODS: The transcriptome and methylome of peripheral monocytes were compared between monozygotic (MZ) twins discordant and concordant for MG, as well as with MG singletons and healthy controls, all females. Sets of differentially expressed genes and differentially methylated CpGs were validated using RT-PCR for expression and target bisulfite sequencing for methylation on additional samples. RESULTS: >100 differentially expressed genes and ∼1800 differentially methylated CpGs were detected in peripheral monocytes between MG patients and controls. Several transcripts associated with immune homeostasis and inflammation resolution were reduced in MG patients. Only a relatively few genes differed between the discordant healthy and MG co-twins, and both their expression and methylation profiles demonstrated very high similarity. INTERPRETATION: This is the first study to characterize the DNA methylation profile in MG, and the expression profile of immune cells in MZ twins with MG. Results suggest that numerous small changes in gene expression or methylation might together contribute to disease. Impaired monocyte function in MG and decreased expression of genes associated with inflammation resolution could contribute to the chronicity of the disease. Findings may serve as potential new predictive biomarkers for disease and disease activity, as well as potential future targets for therapy development. The high similarity between the healthy and the MG discordant twins, suggests that a molecular signature might precede a clinical phenotype, and that genetic predisposition may have a stronger contribution to disease than previously assumed.
Department of Neuromuscular Disorders CHU Salpêtrière Paris 75013 France
Division of Neuroimmunology Lady Davis Carmel Medical Center Haifa 34362 Israel
INSERM U974 CNRS UMR7215 UPMC UM76 AIM Institute of Myology Pitie Salpetriere Paris 73013 France
Rappaport Faculty of Medicine Technion Israel Institute of Technology Haifa 31096 Israel
References provided by Crossref.org
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- $a OBJECTIVE: To identify novel genetic and epigenetic factors associated with Myasthenia gravis (MG) using an identical twins experimental study design. METHODS: The transcriptome and methylome of peripheral monocytes were compared between monozygotic (MZ) twins discordant and concordant for MG, as well as with MG singletons and healthy controls, all females. Sets of differentially expressed genes and differentially methylated CpGs were validated using RT-PCR for expression and target bisulfite sequencing for methylation on additional samples. RESULTS: >100 differentially expressed genes and ∼1800 differentially methylated CpGs were detected in peripheral monocytes between MG patients and controls. Several transcripts associated with immune homeostasis and inflammation resolution were reduced in MG patients. Only a relatively few genes differed between the discordant healthy and MG co-twins, and both their expression and methylation profiles demonstrated very high similarity. INTERPRETATION: This is the first study to characterize the DNA methylation profile in MG, and the expression profile of immune cells in MZ twins with MG. Results suggest that numerous small changes in gene expression or methylation might together contribute to disease. Impaired monocyte function in MG and decreased expression of genes associated with inflammation resolution could contribute to the chronicity of the disease. Findings may serve as potential new predictive biomarkers for disease and disease activity, as well as potential future targets for therapy development. The high similarity between the healthy and the MG discordant twins, suggests that a molecular signature might precede a clinical phenotype, and that genetic predisposition may have a stronger contribution to disease than previously assumed.
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