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Title: Deletion of PREPL, a gene encoding a putative serine oligopeptidase, in patients with hypotonia-cystinuria syndrome
Authors: Jaeken, Jacques
Martens, K
Francois, Inge
Eyskens, F
Lecointre, C
Derua, Rita
Meulemans, S
Slootstra, JW
Waelkens, Etienne
de Zegher, Francis
Creemers, John ×
Matthijs, Gert #
Issue Date: Jan-2006
Publisher: Univ chicago press
Series Title: American Journal of Human Genetics vol:78 issue:1 pages:38-51
Abstract: In 11 patients with a recessive congenital disorder, which we refer to as "the hypotonia-cystinuria syndrome," microdeletion of part of the SLC3A1 and PREPL genes on chromosome 2p21 was found. Patients present with generalized hypotonia at birth, nephrolithiasis, growth hormone deficiency, minor facial dysmorphism, and failure to thrive, followed by hyperphagia and rapid weight gain in late childhood. Since loss-of-function mutations in SLC3A1 are known to cause isolated cystinuria type I, and since the expression of the flanking genes, C2orf34 and PPM1B, was normal, the extended phenotype can be attributed to the deletion of PREPL. PREPL is localized in the cytosol and shows homology with prolyl endopeptidase and oligopeptidase B. Substitution of the predicted catalytic residues (Ser470, Asp556, and His601) by alanines resulted in loss of reactivity with a serine hydrolase-specific probe. In sharp contrast to prolyl oligopeptidase and oligopeptidase B, which require both aminoterminal and carboxyterminal sequences for activity, PREPL activity appears to depend only on the carboxyterminal domain. Taken together, these results suggest that PREPL is a novel oligopeptidase, with unique structural and functional characteristics, involved in hypotonia-cystinuria syndrome.
ISSN: 0002-9297
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Associated Laboratories - miscellaneous (-)
Clinical Genetics Section (-)
Department of Human Genetics - miscellaneous
Section Child - Miscellaneous (-)
Section Newborn (-)
Molecular Genetics Section (-)
Laboratory of Protein Phosphorylation and Proteomics
Pediatric Hematology & Oncology Section (-)
Laboratory of Phosphoproteomics (-)
× corresponding author
# (joint) last author

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