CCG interruptions are unstable and hypermethylated in DM1 patients

Lameiras, S.; Lampraki, E. M.; Kilburn, D.; Alaeitabar, T.; Jamail, I.; Servant, N.; Baulande, S.; Kingan, S. B.; Holt, S.; Gaysinskaya, V.; Brandine, G. D. S.; Stucki, D.; Stojkovic, T.; Bassez, G.; Furling, D.; Gourdon, G.; Tome, S.

doi:10.1101/2024.10.10.617614

bioRxiv · 10.1101/2024.10.10.617614

CCG interruptions are unstable and hypermethylated in DM1 patients

Lameiras, S.·Lampraki, E. M.·Kilburn, D.·Alaeitabar, T.·Jamail, I.·Servant, N.·Baulande, S.·Kingan, S. B.·Holt, S.·Gaysinskaya, V.·Brandine, G. D. S.·Stucki, D.·Stojkovic, T.·Bassez, G.·Furling, D.·Gourdon, G.·Tome, S.

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Abstract

Myotonic dystrophy type 1 (DM1) exhibits highly heterogeneous clinical manifestations caused by an unstable CTG repeat expansion reaching up to 4,000 CTG. The dynamics of CTG repeats and clinical variability depends on the CTG repeat number, CNG repeat interruptions, DNA methylation, somatic mosaicism, but also gene modifiers. Around 10% of the DM1 population carries triplet repeat interruptions (CCG, CGG, CTC, CAG), which differ in number and nature between DM1 families. CCG interruptions have been associated with stabilization of the CTG repeat expansions and a milder phenotype in the DM1 population. However, the dynamics and precise role of interruptions in CTG repeat instability remain relatively underexplored due to the complexities of analyzing them. In this study, we showed that the number of CCG interruptions within the expansion varies within tissues and between generations using single-molecule real-time long-read sequencing. Although the interrupted expanded alleles showed global stabilization, the CCG interruptions themselves displayed variability across generations and within somatic tissues. Importantly, our findings reveal, for the first time, CCG hypermethylation within the CTG expansion, which is linked to downstream hypermethylation of the repeat. These results support the hypothesis that methylation of CCG interruptions within the expanded DMPK alleles may contribute to the stabilization of trinucleotide repeats.

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Lameiras, S., Lampraki, E. M., Kilburn, D., Alaeitabar, T., Jamail, I., Servant, N., Baulande, S., Kingan, S. B., Holt, S., Gaysinskaya, V., Brandine, G. D. S., Stucki, D., Stojkovic, T., Bassez, G., Furling, D., Gourdon, G., Tome, S.. 2024-10-10. CCG interruptions are unstable and hypermethylated in DM1 patients. https://doi.org/10.1101/2024.10.10.617614

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