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Cognitive impairments in adult mice with constitutive inactivation of RIP140 gene expression.
Duclot F., Lapierre M., Fritsch S., White R., Parker M. G., Maurice T., Cavaillès V.
Genes, Brain and Behavior 11, 1 (2012) 69-78 - http://www.hal.inserm.fr/inserm-00631363
(21906262)
Cognitive impairments in adult mice with constitutive inactivation of RIP140 gene expression.
Florian Duclot1, Marion Lapierre2, Samuel Fritsch2, Roger White3, Malcolm Parker3, Tangui Maurice1, Vincent Cavaillès () 2
1 :  MMDN - Mécanismes moléculaires dans les démences neurodégénératives
INSERM : U710 – Université Montpellier II - Sciences et techniques – Ecole Pratique des Hautes Etudes
Universite Montpellier II Place Eugene Bataillon 34095 Montpellier Cedex 5
France
2 :  IRCM - Institut de recherche en cancérologie de Montpellier
INSERM : U896 – Université Montpellier I – CRLCC Val d'Aurelle - Paul Lamarque
208 rue des Apothicaires F-34298 Montpellier
France
3 :  IRDB - Institute for Reproductive and Developmental Biology
http://www1.imperial.ac.uk/medicine/about/institutes/irdb/
Imperial College London
Campus Du Cane Road London, W12 0NN
Royaume-Uni
Behavioral phenotype of RIP140-/- mice
Receptor-interacting protein 140 (RIP140) is a negative transcriptional coregulator of nuclear receptors such as estrogen, retinoic acid or glucocorticoid receptors. Recruitment of RIP140 results in an inhibition of target gene expression through different repressive domains interacting with histone deacetylases or C-terminal binding proteins. In this study, we analyzed the role of RIP140 activity in memory processes using RIP140-deficient transgenic mice. Although the RIP140 protein was clearly expressed in the brain (cortical and hippocampus areas), the morphological examination of RIP140(-/-) mouse brain failed to show grossly observable alterations. Using male 2-month-old RIP140(-/-) , RIP140(+/-) or RIP140(+/+) mice, we did not observe any significant differences in the open-field test, rotarod test and in terms of spontaneous alternation in the Y-maze. By contrast, RIP140(-/-) mice showed long-term memory deficits, with an absence of decrease in escape latencies when animals were tested using a fixed platform position procedure in the water maze and in the passive avoidance test. Noteworthy, RIP140(-/-) mice showed decreased swimming speed, suggesting swimming alterations that may in part account for the marked alterations measured in the water maze. Moreover, RIP140(+/-) and RIP140(-/-) mice showed a significant increase in immobility time in the forced swimming test as compared with wild-type animals. These observations showed that RIP140 gene depletion results in learning and memory deficits as well as stress response, bringing to light a major role for this transcriptional coregulator in the neurophysiological developmental mechanisms underlying cognitive functions.
Sciences du Vivant/Neurosciences
Anglais
1601-1848

Articles dans des revues avec comité de lecture
10.1111/j.1601-183X.2011.00731.x
Genes, Brain and Behavior (Genes Brain Behav)
Publisher Wiley-Blackwell
ISSN 1601-1848 (eISSN : 1601-183X)
internationale
02/2012
19/10/2011
11
1
69-78

RIP140 – transcriptional regulator – learning and memory – behavioral phenotype
Adaptation – Physiological – Adaptor Proteins – Signal Transducing – Animals – Brain – Cognition – Escape Reaction – Exploratory Behavior – Gene Expression Regulation – Gene Silencing – Immobility Response – Tonic – Male – Maze Learning – Memory – Long-Term – Mice – Transgenic – Nuclear Proteins – Rotarod Performance Test – Stress – Psychological – Swimming – Tissue Distribution
This work was supported by CNRS, INSERM and Fondation Jérôme Lejeune (Paris, France).
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