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Overexpression of Down Syndrome Cell Adhesion Molecule impairs precise synaptic targeting

Fragile X syndrome is caused by loss of Fragile X Mental Retardation Protein (FMRP), an RNA binding protein that suppresses protein translation. Here, we identified Down Syndrome Cell Adhesion Molecule (Dscam) RNA, a molecule involved in neural development and implicated in Down syndrome, bound to F...

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Detalles Bibliográficos
Autores principales: Cvetkovska, Vedrana, Hibbert, Alexa D., Emran, Farida, Chen, Brian E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3954815/
https://www.ncbi.nlm.nih.gov/pubmed/23666178
http://dx.doi.org/10.1038/nn.3396
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author Cvetkovska, Vedrana
Hibbert, Alexa D.
Emran, Farida
Chen, Brian E.
author_facet Cvetkovska, Vedrana
Hibbert, Alexa D.
Emran, Farida
Chen, Brian E.
author_sort Cvetkovska, Vedrana
collection PubMed
description Fragile X syndrome is caused by loss of Fragile X Mental Retardation Protein (FMRP), an RNA binding protein that suppresses protein translation. Here, we identified Down Syndrome Cell Adhesion Molecule (Dscam) RNA, a molecule involved in neural development and implicated in Down syndrome, bound to FMRP. Elevated Dscam protein levels in Drosophila FMRP null animals and in animals with three copies of the Dscam gene both produced specific and similar synaptic targeting errors in a hard-wired neural circuit which impaired the animal’s sensory perception. Reducing Dscam levels in FMRP null animals reduced synaptic targeting errors and rescued behavioral responses. Our results demonstrate that excess Dscam protein may be a common molecular mechanism underlying altered neural wiring in major causes of intellectual disability.
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spelling pubmed-39548152014-03-14 Overexpression of Down Syndrome Cell Adhesion Molecule impairs precise synaptic targeting Cvetkovska, Vedrana Hibbert, Alexa D. Emran, Farida Chen, Brian E. Nat Neurosci Article Fragile X syndrome is caused by loss of Fragile X Mental Retardation Protein (FMRP), an RNA binding protein that suppresses protein translation. Here, we identified Down Syndrome Cell Adhesion Molecule (Dscam) RNA, a molecule involved in neural development and implicated in Down syndrome, bound to FMRP. Elevated Dscam protein levels in Drosophila FMRP null animals and in animals with three copies of the Dscam gene both produced specific and similar synaptic targeting errors in a hard-wired neural circuit which impaired the animal’s sensory perception. Reducing Dscam levels in FMRP null animals reduced synaptic targeting errors and rescued behavioral responses. Our results demonstrate that excess Dscam protein may be a common molecular mechanism underlying altered neural wiring in major causes of intellectual disability. 2013-05-12 2013-06 /pmc/articles/PMC3954815/ /pubmed/23666178 http://dx.doi.org/10.1038/nn.3396 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Cvetkovska, Vedrana
Hibbert, Alexa D.
Emran, Farida
Chen, Brian E.
Overexpression of Down Syndrome Cell Adhesion Molecule impairs precise synaptic targeting
title Overexpression of Down Syndrome Cell Adhesion Molecule impairs precise synaptic targeting
title_full Overexpression of Down Syndrome Cell Adhesion Molecule impairs precise synaptic targeting
title_fullStr Overexpression of Down Syndrome Cell Adhesion Molecule impairs precise synaptic targeting
title_full_unstemmed Overexpression of Down Syndrome Cell Adhesion Molecule impairs precise synaptic targeting
title_short Overexpression of Down Syndrome Cell Adhesion Molecule impairs precise synaptic targeting
title_sort overexpression of down syndrome cell adhesion molecule impairs precise synaptic targeting
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3954815/
https://www.ncbi.nlm.nih.gov/pubmed/23666178
http://dx.doi.org/10.1038/nn.3396
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