TY - JOUR
T1 - A current view on contactin-4, -5, and -6
T2 - Implications in neurodevelopmental disorders
AU - Oguro-Ando, Asami
AU - Zuko, Amila
AU - Kleijer, Kristel T.E.
AU - Burbach, J. Peter H.
N1 - Publisher Copyright:
© 2016
PY - 2017/6/1
Y1 - 2017/6/1
N2 - Contactins (Cntns) are a six-member subgroup of the immunoglobulin cell adhesion molecule superfamily (IgCAMs) with pronounced brain expression and function. Recent genetic studies of neuropsychiatric disorders have pinpointed contactin-4 (CNTN4), contactin-5 (CNTN5) and contactin-6 (CNTN6) as candidate genes in neurodevelopmental disorders, particularly in autism spectrum disorders (ASDs), but also in intellectual disability, schizophrenia (SCZ), attention-deficit hyperactivity disorder (ADHD), bipolar disorder (BD), alcohol use disorder (AUD) and anorexia nervosa (AN). This suggests that they have important functions during neurodevelopment. This suggestion is supported by data showing that neurite outgrowth, cell survival and neural circuit formation can be affected by disruption of these genes. Here, we review the current genetic data about their involvement in neuropsychiatric disorders and explore studies on how null mutations affect mouse behavior. Finally, we highlight to role of protein–protein interactions in the potential mechanism of action of Cntn4, -5 and -6 and emphasize that complexes with other membrane proteins may play a role in neuronal developmental functions.
AB - Contactins (Cntns) are a six-member subgroup of the immunoglobulin cell adhesion molecule superfamily (IgCAMs) with pronounced brain expression and function. Recent genetic studies of neuropsychiatric disorders have pinpointed contactin-4 (CNTN4), contactin-5 (CNTN5) and contactin-6 (CNTN6) as candidate genes in neurodevelopmental disorders, particularly in autism spectrum disorders (ASDs), but also in intellectual disability, schizophrenia (SCZ), attention-deficit hyperactivity disorder (ADHD), bipolar disorder (BD), alcohol use disorder (AUD) and anorexia nervosa (AN). This suggests that they have important functions during neurodevelopment. This suggestion is supported by data showing that neurite outgrowth, cell survival and neural circuit formation can be affected by disruption of these genes. Here, we review the current genetic data about their involvement in neuropsychiatric disorders and explore studies on how null mutations affect mouse behavior. Finally, we highlight to role of protein–protein interactions in the potential mechanism of action of Cntn4, -5 and -6 and emphasize that complexes with other membrane proteins may play a role in neuronal developmental functions.
KW - ADHD
KW - Alcohol use disorder
KW - Anorexia nervosa
KW - Autism
KW - Bipolar disorder
KW - Cell adhesion molecules
KW - Contactin
KW - IgCAMs
KW - Neurodevelopmental disorder
KW - Neuropsychiatric disorder
KW - Schizophrenia
UR - http://www.scopus.com/inward/record.url?scp=85009781791&partnerID=8YFLogxK
U2 - 10.1016/j.mcn.2016.12.004
DO - 10.1016/j.mcn.2016.12.004
M3 - Review article
C2 - 28064060
SN - 1044-7431
VL - 81
SP - 72
EP - 83
JO - Molecular and Cellular Neuroscience
JF - Molecular and Cellular Neuroscience
ER -