Author
Listed:
- Victor Briz
(KU Leuven
VIB Center for Brain & Disease Research, Department of Neurosciences KU Leuven)
- Leonardo Restivo
(Institute of Cell Biology and Neurobiology, CNR
Hospital for Sick Children
University of Lausanne)
- Emanuela Pasciuto
(KU Leuven
VIB Center for Brain & Disease Research, Department of Neurosciences KU Leuven
KU Leuven)
- Konrad Juczewski
(Karolinska Institutet
National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health)
- Valentina Mercaldo
(KU Leuven
Hospital for Sick Children
University of Lausanne)
- Adrian C. Lo
(KU Leuven
VIB Center for Brain & Disease Research, Department of Neurosciences KU Leuven
University of Lausanne)
- Pieter Baatsen
(VIB Electron Microscopy Platform & Bio Imaging Core, VIB-KU Leuven Center for Brain & Disease Research, Department of Neurosciences KU Leuven)
- Natalia V. Gounko
(VIB Electron Microscopy Platform & Bio Imaging Core, VIB-KU Leuven Center for Brain & Disease Research, Department of Neurosciences KU Leuven)
- Antonella Borreca
(KU Leuven
VIB Center for Brain & Disease Research, Department of Neurosciences KU Leuven
Institute of Cell Biology and Neurobiology, CNR
University of Rome Tor Vergata)
- Tiziana Girardi
(VIB Center for Brain & Disease Research, Department of Neurosciences KU Leuven)
- Rossella Luca
(KU Leuven
VIB Center for Brain & Disease Research, Department of Neurosciences KU Leuven
Institute of Cell Biology and Neurobiology, CNR)
- Julie Nys
(KU Leuven
VIB Center for Brain & Disease Research, Department of Neurosciences KU Leuven
KU Leuven)
- Rogier B. Poorthuis
(VU University)
- Huibert D. Mansvelder
(VU University)
- Gilberto Fisone
(Karolinska Institutet)
- Martine Ammassari-Teule
(Institute of Cell Biology and Neurobiology, CNR)
- Lutgarde Arckens
(KU Leuven)
- Patrik Krieger
(Karolinska Institutet
Ruhr-University)
- Rhiannon Meredith
(VU University)
- Claudia Bagni
(KU Leuven
VIB Center for Brain & Disease Research, Department of Neurosciences KU Leuven
University of Lausanne
University of Rome Tor Vergata)
Abstract
The brain cytoplasmic (BC1) RNA is a non-coding RNA (ncRNA) involved in neuronal translational control. Absence of BC1 is associated with altered glutamatergic transmission and maladaptive behavior. Here, we show that pyramidal neurons in the barrel cortex of BC1 knock out (KO) mice display larger excitatory postsynaptic currents and increased spontaneous activity in vivo. Furthermore, BC1 KO mice have enlarged spine heads and postsynaptic densities and increased synaptic levels of glutamate receptors and PSD-95. Of note, BC1 KO mice show aberrant structural plasticity in response to whisker deprivation, impaired texture novel object recognition and altered social behavior. Thus, our study highlights a role for BC1 RNA in experience-dependent plasticity and learning in the mammalian adult neocortex, and provides insight into the function of brain ncRNAs regulating synaptic transmission, plasticity and behavior, with potential relevance in the context of intellectual disabilities and psychiatric disorders.
Suggested Citation
Victor Briz & Leonardo Restivo & Emanuela Pasciuto & Konrad Juczewski & Valentina Mercaldo & Adrian C. Lo & Pieter Baatsen & Natalia V. Gounko & Antonella Borreca & Tiziana Girardi & Rossella Luca & J, 2017.
"The non-coding RNA BC1 regulates experience-dependent structural plasticity and learning,"
Nature Communications, Nature, vol. 8(1), pages 1-16, December.
Handle:
RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_s41467-017-00311-2
DOI: 10.1038/s41467-017-00311-2
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