Truncating Neurotrypsin Mutation in Autosomal Recessive Nonsyndromic Mental Retardation - Archive ouverte HAL
Article Dans Une Revue Science Année : 2002

Truncating Neurotrypsin Mutation in Autosomal Recessive Nonsyndromic Mental Retardation

Truncating neurotrypsin mutation in autosomal recessive nonsyndromic mental retardation.

Résumé

A 4-base pair deletion in the neuronal serine protease neurotrypsin gene was associated with autosomal recessive nonsyndromic mental retardation (MR). In situ hybridization experiments on human fetal brains showed that neurotrypsin was highly expressed in brain structures involved in learning and memory. Immuno-electron microscopy on adult human brain sections revealed that neurotrypsin is located in presynaptic nerve endings, particularly over the presynaptic membrane lining the synaptic cleft. These findings suggest that neurotrypsin-mediated proteolysis is required for normal synaptic function and suggest potential insights into the pathophysiological bases of mental retardation.
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Dates et versions

hal-02124683 , version 1 (09-05-2019)

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Florence Molinari, Marlène Rio, Virginia Meskenaite, Férechté Encha-Razavi, Joelle Augé, et al.. Truncating Neurotrypsin Mutation in Autosomal Recessive Nonsyndromic Mental Retardation. Science, 2002, 298 (5599), pp.1779-1781. ⟨10.1126/science.1076521⟩. ⟨hal-02124683⟩
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