作者
Payam Mohassel,Sandra Donkervoort,Museer A. Lone,Matthew Nalls,Kenneth Gable,Sita D. Gupta,A. Reghan Foley,Ying Hu,Jonas Alex Morales Saute,Ana Lucila Moreira,Fernando Kok,Alessandro Introna,Giancarlo Logroscino,Christopher Grunseich,Alec R. Nickolls,Naemeh Pourshafie,Sarah Neuhaus,Dimah Saade,Andrea Gangfuß,Heike Kölbel,Zoe Piccus,Claire E. Le Pichon,Chiara Fiorillo,Cindy V. Ly,Ana Töpf,Lauren Brady,Sabine Specht,Aliza Zidell,Hélio Pedro,Eric Mittelmann,Florian P. Thomas,Katherine R. Chao,Chamindra G. Konersman,Megan T. Cho,Tracy Brandt,Volker Straub,Anne M. Connolly,Ulrike Schara,Andreas Roos,Mark A. Tarnopolsky,Ahmet Höke,Robert H. Brown,Chia‐Hsueh Lee,Thorsten Hornemann,Teresa Dunn,Carsten G. Bönnemann
摘要
Amyotrophic lateral sclerosis (ALS) is a progressive, neurodegenerative disease of the lower and upper motor neurons with sporadic or hereditary occurrence. Age of onset, pattern of motor neuron degeneration and disease progression vary widely among individuals with ALS. Various cellular processes may drive ALS pathomechanisms, but a monogenic direct metabolic disturbance has not been causally linked to ALS. Here we show SPTLC1 variants that result in unrestrained sphingoid base synthesis cause a monogenic form of ALS. We identified four specific, dominantly acting SPTLC1 variants in seven families manifesting as childhood-onset ALS. These variants disrupt the normal homeostatic regulation of serine palmitoyltransferase (SPT) by ORMDL proteins, resulting in unregulated SPT activity and elevated levels of canonical SPT products. Notably, this is in contrast with SPTLC1 variants that shift SPT amino acid usage from serine to alanine, result in elevated levels of deoxysphingolipids and manifest with the alternate phenotype of hereditary sensory and autonomic neuropathy. We custom designed small interfering RNAs that selectively target the SPTLC1 ALS allele for degradation, leave the normal allele intact and normalize sphingolipid levels in vitro. The role of primary metabolic disturbances in ALS has been elusive; this study defines excess sphingolipid biosynthesis as a fundamental metabolic mechanism for motor neuron disease. Clinical and genetic evaluation of individuals with childhood-onset amyotrophic lateral sclerosis identifies a new monogenic cause for early-onset ALS and proposes a specific metabolic mechanism leading to motor neuron disease via sphingolipid excess.