Huntington's disease age at motor onset is modified by the tandem hexamer repeat in TCERG1

Lobanov, S. V.; McAllister, B.; McDade-Kumar, M.; Landwehrmeyer, G. B.; Rosser, A. E.; REGISTRY Investigators of the European Huntington's disease network,; Paulsen, J. S.; PREDICT-HD Investigators of the Huntington Study Group,; Lee, J.-M.; MacDonald, M. E.; Gusella, J.; Ryten, M.; Williams, N.; Holmans, P.; Massey, T. H.; Jones, L.

doi:10.1101/2021.07.16.452643

bioRxiv · 10.1101/2021.07.16.452643

Huntington's disease age at motor onset is modified by the tandem hexamer repeat in TCERG1

Lobanov, S. V.·McAllister, B.·McDade-Kumar, M.·Landwehrmeyer, G. B.·Rosser, A. E.·REGISTRY Investigators of the European Huntington's disease network,·Paulsen, J. S.·PREDICT-HD Investigators of the Huntington Study Group,·Lee, J.-M.·MacDonald, M. E.·Gusella, J.·Ryten, M.·Williams, N.·Holmans, P.·Massey, T. H.·Jones, L.

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Abstract

BackgroundHuntingtons disease is caused by an expanded CAG tract in HTT. The length of the CAG tract accounts for over half the variance in age at onset of disease, and is influenced by other genetic factors, mostly implicating the DNA maintenance machinery. We examined a single nucleotide variant, rs79727797, on chromosome 5 in the TCERG1 gene, previously reported to be associated with Huntingtons disease and a quasi-tandem repeat (QTR) hexamer in exon 4 of TCERG1 with a central pure repeat. MethodsWe developed a novel method for calling perfect and imperfect repeats from exome sequencing data, and tested association between the QTR in TCERG1 and residual age at motor onset (after correcting for the effects of CAG length in the HTT gene) in 610 individuals with Huntingtons disease via regression analysis. ResultsWe found a significant association between age at onset and the sum of the repeat lengths from both alleles of the QTR (p = 2.1x10-9), with each added repeat hexamer reducing age at onset by one year (95% confidence interval [0.7, 1.4]). This association explained that previously observed with rs79727797. ConclusionsThe association with age at onset in the genome-wide association study is due to a QTR hexamer in TCERG1, translated to a glutamine/alanine tract in the protein. We could not distinguish whether this was due to cis-effects of the hexamer repeat on gene expression or of the encoded glutamine/alanine tract in the protein. These results motivate further study of the mechanisms by which TCERG1 modifies onset of HD.

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Lobanov, S. V., McAllister, B., McDade-Kumar, M., Landwehrmeyer, G. B., Rosser, A. E., REGISTRY Investigators of the European Huntington's disease network,, Paulsen, J. S., PREDICT-HD Investigators of the Huntington Study Group,, Lee, J.-M., MacDonald, M. E., Gusella, J., Ryten, M., Williams, N., Holmans, P., Massey, T. H., Jones, L.. 2021-07-19. Huntington's disease age at motor onset is modified by the tandem hexamer repeat in TCERG1. https://doi.org/10.1101/2021.07.16.452643

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