Recessive loss of function of the neuronal ubiquitin hydrolase UCHL1 leads to early-onset progressive neurodegeneration.

TitleRecessive loss of function of the neuronal ubiquitin hydrolase UCHL1 leads to early-onset progressive neurodegeneration.
Publication TypeJournal Article
Year of Publication2013
AuthorsBilguvar, K, Tyagi, NK, Ozkara, C, Tuysuz, B, Bakircioglu, M, Choi, M, Delil, S, Çağlayan, AO, Baranoski, JF, Erturk, O, Yalcinkaya, C, Karacorlu, M, Dincer, A, Johnson, MH, Mane, S, Chandra, SS, Louvi, A, Boggon, TJ, Lifton, RP, Horwich, AL, Günel, M
JournalProc Natl Acad Sci U S A
Date Published2013 Feb 26
KeywordsAdult, Age of Onset, Amino Acid Sequence, Base Sequence, Child, Preschool, Exome, Female, Genes, Recessive, Homozygote, Humans, Hydrolysis, Male, Models, Molecular, Molecular Sequence Data, Mutation, Missense, Nerve Degeneration, Neurons, Pedigree, Protein Binding, Sequence Analysis, DNA, Substrate Specificity, Syndrome, Thermodynamics, Ubiquitin, Ubiquitin Thiolesterase

Ubiquitin C-terminal hydrolase-L1 (UCHL1), a neuron-specific de-ubiquitinating enzyme, is one of the most abundant proteins in the brain. We describe three siblings from a consanguineous union with a previously unreported early-onset progressive neurodegenerative syndrome featuring childhood onset blindness, cerebellar ataxia, nystagmus, dorsal column dysfuction, and spasticity with upper motor neuron dysfunction. Through homozygosity mapping of the affected individuals followed by whole-exome sequencing of the index case, we identified a previously undescribed homozygous missense mutation within the ubiquitin binding domain of UCHL1 (UCHL1(GLU7ALA)), shared by all affected subjects. As demonstrated by isothermal titration calorimetry, purified UCHL1(GLU7ALA), compared with WT, exhibited at least sevenfold reduced affinity for ubiquitin. In vitro, the mutation led to a near complete loss of UCHL1 hydrolase activity. The GLU7ALA variant is predicted to interfere with the substrate binding by restricting the proper positioning of the substrate for tunneling underneath the cross-over loop spanning the catalytic cleft of UCHL1. This interference with substrate binding, combined with near complete loss of hydrolase activity, resulted in a >100-fold reduction in the efficiency of UCHL1(GLU7ALA) relative to WT. These findings demonstrate a broad requirement of UCHL1 in the maintenance of the nervous system.

Alternate JournalProc. Natl. Acad. Sci. U.S.A.
PubMed ID23359680
PubMed Central IDPMC3587195
Grant ListUL1 RR024139 / RR / NCRR NIH HHS / United States
U24 NS051869 / NS / NINDS NIH HHS / United States
U24 NS051869-02S1 / NS / NINDS NIH HHS / United States
RC2 NS070477 / NS / NINDS NIH HHS / United States
U54HG006504 / HG / NHGRI NIH HHS / United States
U54 HG006504 / HG / NHGRI NIH HHS / United States
/ / Howard Hughes Medical Institute / United States