TY - JOUR
T1 - Neuroanatomical and behavioral deficits in mice haploinsufficient for Pericentriolar material 1 (Pcm1)
AU - Zoubovsky, Sandra
AU - Oh, Edwin C.
AU - Cash-Padgett, Tyler
AU - Johnson, Alexander W.
AU - Hou, Zhipeng
AU - Mori, Susumu
AU - Gallagher, Michela
AU - Katsanis, Elias Nicholas
AU - Sawa, Akira
AU - Jaaro-Peled, Hanna
N1 - Funding Information:
This research was funded by MH-084018 , MH-094268 Silvo O. Conte Center , MH-069853 , MH-085226 , MH-088753 , MH-092443 , MH-105660 , as well as grants from Stanley , S-R , RUSK , NARSAD , and MSCRF .
Publisher Copyright:
© 2015 Elsevier Ireland Ltd and the Japan Neuroscience Society.
PY - 2015/9/1
Y1 - 2015/9/1
N2 - The pericentriolar material (PCM) is composed of proteins responsible for microtubule nucleation/anchoring at the centrosome, some of which have been associated with genetic susceptibility to schizophrenia. Here, we show that mice haploinsufficient for Pericentriolar material 1 (Pcm1+/-), which encodes a component of the PCM found to bear rare loss of function mutations in patients with psychiatric illness, manifest neuroanatomical phenotypes and behavioral abnormalities. Using ex vivo magnetic resonance imaging of the Pcm1+/- brain, we detect reduced whole brain volume. Pcm1 mutant mice show impairment in social interaction, specifically in the social novelty phase, but not in the sociability phase of the three-chamber social interaction test. In contrast, Pcm1+/- mice show normal preference for a novel object, suggesting specific impairment in response to novel social stimulus. In addition, Pcm1+/- mice display significantly reduced rearing activity in the open field. Pcm1+/- mice behave normally in the elevated plus maze, rotarod, prepulse inhibition, and progressive ratio tests. Together, our results suggest that haploinsufficiency at the Pcm1 locus can induce a range of neuroanatomical and behavioral phenotypes that support the candidacy of this locus in neuropsychiatric disorders.
AB - The pericentriolar material (PCM) is composed of proteins responsible for microtubule nucleation/anchoring at the centrosome, some of which have been associated with genetic susceptibility to schizophrenia. Here, we show that mice haploinsufficient for Pericentriolar material 1 (Pcm1+/-), which encodes a component of the PCM found to bear rare loss of function mutations in patients with psychiatric illness, manifest neuroanatomical phenotypes and behavioral abnormalities. Using ex vivo magnetic resonance imaging of the Pcm1+/- brain, we detect reduced whole brain volume. Pcm1 mutant mice show impairment in social interaction, specifically in the social novelty phase, but not in the sociability phase of the three-chamber social interaction test. In contrast, Pcm1+/- mice show normal preference for a novel object, suggesting specific impairment in response to novel social stimulus. In addition, Pcm1+/- mice display significantly reduced rearing activity in the open field. Pcm1+/- mice behave normally in the elevated plus maze, rotarod, prepulse inhibition, and progressive ratio tests. Together, our results suggest that haploinsufficiency at the Pcm1 locus can induce a range of neuroanatomical and behavioral phenotypes that support the candidacy of this locus in neuropsychiatric disorders.
KW - Behavior
KW - Mouse model
KW - Neuroanatomy
KW - Pcm1
KW - Schizophrenia
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U2 - 10.1016/j.neures.2015.02.002
DO - 10.1016/j.neures.2015.02.002
M3 - Article
C2 - 25697395
AN - SCOPUS:84938200417
SN - 0168-0102
VL - 98
SP - 45
EP - 49
JO - Neuroscience Research
JF - Neuroscience Research
ER -