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Novel pathogenic mechanisms of congenital insensitivity to pain with anhidrosis genetic disorder unveiled by functional analysis of neurotrophic tyrosine receptor kinase type 1/nerve growth factor receptor mutations

Item Type:Article
Title:Novel pathogenic mechanisms of congenital insensitivity to pain with anhidrosis genetic disorder unveiled by functional analysis of neurotrophic tyrosine receptor kinase type 1/nerve growth factor receptor mutations
Creators Name:Miranda, C. and Di Virgilio, M. and Selleri, S. and Zanotti, G. and Pagliardini, S. and Pierotti, M.A. and Greco, A.
Abstract:Congenital insensitivity to pain with anhidrosis (CIPA) is a rare genetic disease characterized by absence of reaction to noxious stimuli and anhidrosis. The genetic bases of CIPA have remained long unknown. A few years ago, point mutations affecting both coding and noncoding regions of the neurotrophic tyrosine receptor kinase type 1 (NTRK1)/nerve growth factor receptor gene have been detected in CIPA patients, demonstrating the implication of the nerve growth factor/NTRK1 pathway in the pathogenesis of the disease. We have previously shown that two CIPA mutations, the G571R and the R774P, inactivate the NTRK1 receptor by interfering with the autophosphorylation process. We have extended our functional analysis to seven additional NTRK1 mutations associated with CIPA recently reported by others. Through a combination of biochemical and biological assays, we have identified polymorphisms and pathogenic mutations. In addition to the identification of residues important for NTRK1 activity, our analysis suggests the existence of two novel pathogenic mechanisms in CIPA: one based on the NTRK1 receptor processing and the other acting through the reduction of the receptor activity.
Keywords:Amino Acid Substitution, Congenital Pain Insensitivity, COS Cells, Hypohidrosis, Kinetics, Missense Mutation, Mutation, Nerve Growth Factor, Nerve Growth Factor Receptor , Recombinant Proteins, Signal Transduction, Transfection, trkA Receptor , Animals, Cercopithecus aethiops
Source:Journal of Biological Chemistry
ISSN:0021-9258
Publisher:American Society for Biochemistry and Molecular Biology
Volume:277
Number:8
Page Range:6455-6462
Date:22 February 2002
Official Publication:https://doi.org/10.1074/jbc.M110016200
PubMed:View item in PubMed

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