Cargando…
Brain Phenotype of Transgenic Mice Overexpressing Cystathionine β-Synthase
BACKGROUND: The cystathionine β-synthase (CBS) gene, located on human chromosome 21q22.3, is a good candidate for playing a role in the Down Syndrome (DS) cognitive profile: it is overexpressed in the brain of individuals with DS, and it encodes a key enzyme of sulfur-containing amino acid (SAA) met...
Autores principales: | , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3257219/ https://www.ncbi.nlm.nih.gov/pubmed/22253703 http://dx.doi.org/10.1371/journal.pone.0029056 |
_version_ | 1782221122568192000 |
---|---|
author | Régnier, Vinciane Billard, Jean-Marie Gupta, Sapna Potier, Brigitte Woerner, Stéphanie Paly, Evelyne Ledru, Aurélie David, Sabrina Luilier, Sabrina Bizot, Jean-Charles Vacano, Guido Kraus, Jan P. Patterson, David Kruger, Warren D. Delabar, Jean M. London, Jaqueline |
author_facet | Régnier, Vinciane Billard, Jean-Marie Gupta, Sapna Potier, Brigitte Woerner, Stéphanie Paly, Evelyne Ledru, Aurélie David, Sabrina Luilier, Sabrina Bizot, Jean-Charles Vacano, Guido Kraus, Jan P. Patterson, David Kruger, Warren D. Delabar, Jean M. London, Jaqueline |
author_sort | Régnier, Vinciane |
collection | PubMed |
description | BACKGROUND: The cystathionine β-synthase (CBS) gene, located on human chromosome 21q22.3, is a good candidate for playing a role in the Down Syndrome (DS) cognitive profile: it is overexpressed in the brain of individuals with DS, and it encodes a key enzyme of sulfur-containing amino acid (SAA) metabolism, a pathway important for several brain physiological processes. METHODOLOGY/PRINCIPAL FINDINGS: Here, we have studied the neural consequences of CBS overexpression in a transgenic mouse line (60.4P102D1) expressing the human CBS gene under the control of its endogenous regulatory regions. These mice displayed a ∼2-fold increase in total CBS proteins in different brain areas and a ∼1.3-fold increase in CBS activity in the cerebellum and the hippocampus. No major disturbance of SAA metabolism was observed, and the transgenic mice showed normal behavior in the rotarod and passive avoidance tests. However, we found that hippocampal synaptic plasticity is facilitated in the 60.4P102D1 line. CONCLUSION/SIGNIFICANCE: We demonstrate that CBS overexpression has functional consequences on hippocampal neuronal networks. These results shed new light on the function of the CBS gene, and raise the interesting possibility that CBS overexpression might have an advantageous effect on some cognitive functions in DS. |
format | Online Article Text |
id | pubmed-3257219 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-32572192012-01-17 Brain Phenotype of Transgenic Mice Overexpressing Cystathionine β-Synthase Régnier, Vinciane Billard, Jean-Marie Gupta, Sapna Potier, Brigitte Woerner, Stéphanie Paly, Evelyne Ledru, Aurélie David, Sabrina Luilier, Sabrina Bizot, Jean-Charles Vacano, Guido Kraus, Jan P. Patterson, David Kruger, Warren D. Delabar, Jean M. London, Jaqueline PLoS One Research Article BACKGROUND: The cystathionine β-synthase (CBS) gene, located on human chromosome 21q22.3, is a good candidate for playing a role in the Down Syndrome (DS) cognitive profile: it is overexpressed in the brain of individuals with DS, and it encodes a key enzyme of sulfur-containing amino acid (SAA) metabolism, a pathway important for several brain physiological processes. METHODOLOGY/PRINCIPAL FINDINGS: Here, we have studied the neural consequences of CBS overexpression in a transgenic mouse line (60.4P102D1) expressing the human CBS gene under the control of its endogenous regulatory regions. These mice displayed a ∼2-fold increase in total CBS proteins in different brain areas and a ∼1.3-fold increase in CBS activity in the cerebellum and the hippocampus. No major disturbance of SAA metabolism was observed, and the transgenic mice showed normal behavior in the rotarod and passive avoidance tests. However, we found that hippocampal synaptic plasticity is facilitated in the 60.4P102D1 line. CONCLUSION/SIGNIFICANCE: We demonstrate that CBS overexpression has functional consequences on hippocampal neuronal networks. These results shed new light on the function of the CBS gene, and raise the interesting possibility that CBS overexpression might have an advantageous effect on some cognitive functions in DS. Public Library of Science 2012-01-12 /pmc/articles/PMC3257219/ /pubmed/22253703 http://dx.doi.org/10.1371/journal.pone.0029056 Text en Régnier et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Régnier, Vinciane Billard, Jean-Marie Gupta, Sapna Potier, Brigitte Woerner, Stéphanie Paly, Evelyne Ledru, Aurélie David, Sabrina Luilier, Sabrina Bizot, Jean-Charles Vacano, Guido Kraus, Jan P. Patterson, David Kruger, Warren D. Delabar, Jean M. London, Jaqueline Brain Phenotype of Transgenic Mice Overexpressing Cystathionine β-Synthase |
title | Brain Phenotype of Transgenic Mice Overexpressing Cystathionine β-Synthase |
title_full | Brain Phenotype of Transgenic Mice Overexpressing Cystathionine β-Synthase |
title_fullStr | Brain Phenotype of Transgenic Mice Overexpressing Cystathionine β-Synthase |
title_full_unstemmed | Brain Phenotype of Transgenic Mice Overexpressing Cystathionine β-Synthase |
title_short | Brain Phenotype of Transgenic Mice Overexpressing Cystathionine β-Synthase |
title_sort | brain phenotype of transgenic mice overexpressing cystathionine β-synthase |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3257219/ https://www.ncbi.nlm.nih.gov/pubmed/22253703 http://dx.doi.org/10.1371/journal.pone.0029056 |
work_keys_str_mv | AT regniervinciane brainphenotypeoftransgenicmiceoverexpressingcystathioninebsynthase AT billardjeanmarie brainphenotypeoftransgenicmiceoverexpressingcystathioninebsynthase AT guptasapna brainphenotypeoftransgenicmiceoverexpressingcystathioninebsynthase AT potierbrigitte brainphenotypeoftransgenicmiceoverexpressingcystathioninebsynthase AT woernerstephanie brainphenotypeoftransgenicmiceoverexpressingcystathioninebsynthase AT palyevelyne brainphenotypeoftransgenicmiceoverexpressingcystathioninebsynthase AT ledruaurelie brainphenotypeoftransgenicmiceoverexpressingcystathioninebsynthase AT davidsabrina brainphenotypeoftransgenicmiceoverexpressingcystathioninebsynthase AT luiliersabrina brainphenotypeoftransgenicmiceoverexpressingcystathioninebsynthase AT bizotjeancharles brainphenotypeoftransgenicmiceoverexpressingcystathioninebsynthase AT vacanoguido brainphenotypeoftransgenicmiceoverexpressingcystathioninebsynthase AT krausjanp brainphenotypeoftransgenicmiceoverexpressingcystathioninebsynthase AT pattersondavid brainphenotypeoftransgenicmiceoverexpressingcystathioninebsynthase AT krugerwarrend brainphenotypeoftransgenicmiceoverexpressingcystathioninebsynthase AT delabarjeanm brainphenotypeoftransgenicmiceoverexpressingcystathioninebsynthase AT londonjaqueline brainphenotypeoftransgenicmiceoverexpressingcystathioninebsynthase |