Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis

Abstract

There is a strong genetic contribution to Amyotrophic lateral sclerosis (ALS) risk, with heritability estimates of up to 60%. Both Mendelian and small effect variants have been identified, but in common with other conditions, such variants only explain a little of the heritability. Genomic structural variation might account for some of this otherwise unexplained heritability. We therefore investigated association between structural variation in a set of 25 ALS genes, and ALS risk and phenotype. As expected, the repeat expansion in the C9orf72 gene was identified as associated with ALS. Two other ALS-associated structural variants were identified: inversion in the VCP gene and insertion in the ERBB4 gene. All three variants were associated both with increased risk of ALS and specific phenotypic patterns of disease expression. More than 70% of people with respiratory onset ALS harboured ERBB4 insertion compared with 25% of the general population, suggesting respiratory onset ALS may be a distinct genetic subtype.

Metadata

Authors/Creators:

Al Khleifat, A.
Iacoangeli, A.
van Vugt, J.J.F.A.
Bowles, H.
Moisse, M.
Zwamborn, R.A.J.
van der Spek, R.A.A.
Shatunov, A.
Cooper-Knock, J. https://orcid.org/0000-0002-0873-8689
Topp, S.
Byrne, R.
Gellera, C.
López, V.
Jones, A.R.
Opie-Martin, S.
Vural, A.
Campos, Y.
van Rheenen, W.
Kenna, B.
Van Eijk, K.R.
Kenna, K.
Weber, M.
Smith, B.
Fogh, I.
Silani, V.
Morrison, K.E.
Dobson, R.
van Es, M.A.
McLaughlin, R.L.
Vourc’h, P.
Chio, A.
Corcia, P.
de Carvalho, M.
Gotkine, M.
Panades, M.P.
Mora, J.S.
Shaw, P.J. https://orcid.org/0000-0002-8925-2567
Landers, J.E.
Glass, J.D.
Shaw, C.E.
Basak, N.
Hardiman, O.
Robberecht, W.
Van Damme, P.
van den Berg, L.H.
Veldink, J.H.
Al-Chalabi, A.

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