The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter

• Published in: Molecular psychiatry Vol. 21; no. 8; pp. 1112 - 1124
• Main Authors: Gijselinck, I, Van Mossevelde, S, van der Zee, J, Sieben, A, Engelborghs, S, De Bleecker, J, Ivanoiu, A, Deryck, O, Edbauer, D, Zhang, M, Heeman, B, Bäumer, V, Van den Broeck, M, Mattheijssens, M, Peeters, K, Rogaeva, E, De Jonghe, P, Cras, P, Martin, J-J, de Deyn, P P, Cruts, M, Van Broeckhoven, C
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 01.08.2016; Nature Publishing Group
• Subjects: 13/109; 13/51; 38/77; 45/29; 631/208; 631/337; 631/378; Adult; Age of Onset; Amyotrophic lateral sclerosis; Amyotrophic Lateral Sclerosis - genetics; Amyotrophic Lateral Sclerosis - metabolism; Analysis; Behavioral Sciences; Belgium; Biological Psychology; Brain diseases; Brain research; C9orf72 Protein; Care and treatment; CpG Islands - genetics; DNA methylation; DNA Methylation - genetics; Down-Regulation; Epigenesis, Genetic - genetics; Epigenomics - methods; Female; Frontotemporal Lobar Degeneration - genetics; Frontotemporal Lobar Degeneration - metabolism; Genetic aspects; Genetic Predisposition to Disease - genetics; Genetic transcription; Hospitals; Humans; Male; Medicine; Medicine & Public Health; Methylation; Middle Aged; Neurology; Neurosciences; Original; original-article; Pharmacotherapy; Promoter Regions, Genetic - genetics; Proteins - genetics; Proteins - metabolism; Psychiatry; Belgium; Canada; Toronto Ontario Canada; Germany
• ISSN: 1359-4184; 1476-5578
• DOI: 10.1038/mp.2015.159

Pathological expansion of a G 4 C 2 repeat, located in the 5' regulatory region of C9orf72 , is the most common genetic cause of frontotemporal lobar degeneration (FTLD) and amyotrophic lateral sclerosis (ALS). C9orf72 patients have highly variable onset ages suggesting the presence of modifying factors and/or anticipation. We studied 72 Belgian index patients with FTLD, FTLD–ALS or ALS and 61 relatives with a C9orf72 repeat expansion. We assessed the effect of G 4 C 2 expansion size on onset age, the role of anticipation and the effect of repeat size on methylation and C9orf72 promoter activity. G 4 C 2 expansion sizes varied in blood between 45 and over 2100 repeat units with short expansions (45–78 units) present in 5.6% of 72 index patients with an expansion. Short expansions co-segregated with disease in two families. The subject with a short expansion in blood but an indication of mosaicism in brain showed the same pathology as those with a long expansion. Further, we provided evidence for an association of G 4 C 2 expansion size with onset age ( P <0.05) most likely explained by an association of methylation state of the 5' flanking CpG island and expansion size in blood ( P <0.0001) and brain ( P <0.05). In several informative C9orf72 parent–child transmissions, we identified earlier onset ages, increasing expansion sizes and/or increasing methylation states ( P =0.0034) of the 5' CpG island, reminiscent of disease anticipation. Also, intermediate repeats (7–24 units) showed a slightly higher methylation degree ( P <0.0001) and a decrease of C9orf72 promoter activity ( P <0.0001) compared with normal short repeats (2–6 units). Decrease of transcriptional activity was even more prominent in the presence of small deletions flanking G 4 C 2 ( P <0.0001). Here we showed that increased methylation of CpGs in the C9orf72 promoter may explain how an increasing G 4 C 2 size lead to loss-of-function without excluding repeat length-dependent toxic gain-of-function. These data provide insights into disease mechanisms and have important implications for diagnostic counseling and potential therapeutic approaches.