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

dc.contributor.authorBilguvar, Kaya
dc.contributor.authorTyagi, Navneet K.
dc.contributor.authorOzkara, Cigdem
dc.contributor.authorTuysuz, Beyhan
dc.contributor.authorBakircioglu, Mehmet
dc.contributor.authorChoi, Murim
dc.contributor.authorDelil, Sakir
dc.contributor.authorCaglayan, Ahmet O.
dc.contributor.authorBaranoski, Jacob F.
dc.contributor.authorErturk, Ozdem
dc.contributor.authorYalcinkaya, Cengiz
dc.contributor.authorKaracorlu, Murat
dc.contributor.authorDincer, Alp
dc.contributor.authorJohnson, Michele H.
dc.contributor.authorMane, Shrikant
dc.contributor.authorChandra, Sreeganga S.
dc.contributor.authorLouvi, Angeliki
dc.contributor.authorBoggon, Titus J.
dc.contributor.authorLifton, Richard P.
dc.contributor.authorHorwich, Arthur L.
dc.contributor.authorGunel, Murat
dc.date.accessioned2023-02-21T12:38:29Z
dc.date.available2023-02-21T12:38:29Z
dc.date.issued2013-01-01
dc.description.abstractUbiquitin C-terminal hydrolase-L1 (UCHL1), a neuron-specific deubiquitinating 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.
dc.description.issue9
dc.description.issueFEB 26
dc.description.pages3489-3494
dc.description.volume110
dc.identifier.doi10.1073/pnas.1222732110
dc.identifier.urihttps://hdl.handle.net/11443/2389
dc.identifier.urihttp://dx.doi.org/10.1073/pnas.1222732110
dc.identifier.wosWOS:000315841900060
dc.publisherNATL ACAD SCIENCES
dc.relation.ispartofPROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
dc.subjectprotein quality control
dc.subjectrecessive inherited neurodegeneration
dc.titleRecessive loss of function of the neuronal ubiquitin hydrolase UCHL1 leads to early-onset progressive neurodegeneration
dc.typeArticle

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