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关于接触蛋白4、5和6的当前观点:对神经发育障碍的影响。

A current view on contactin-4, -5, and -6: Implications in neurodevelopmental disorders.

作者信息

Oguro-Ando Asami, Zuko Amila, Kleijer Kristel T E, Burbach J Peter H

机构信息

Department of Translational Neuroscience, Brain Center Rudolf Magnus, University Medical Center Utrecht, Universiteitsweg 100, 3584CG Utrecht, The Netherlands; University of Exeter Medical School, Wellcome Wolfson Centre for Medical Research, RILD Building, Barrack Road, Exeter EX2 5DW, UK.

Department of Translational Neuroscience, Brain Center Rudolf Magnus, University Medical Center Utrecht, Universiteitsweg 100, 3584CG Utrecht, The Netherlands; RIKEN Brain Science Institute, 2-1 Hirosawa, Wako, Saitama 351-0198, Japan.

出版信息

Mol Cell Neurosci. 2017 Jun;81:72-83. doi: 10.1016/j.mcn.2016.12.004. Epub 2017 Jan 5.

Abstract

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.

摘要

接触蛋白(Cntns)是免疫球蛋白细胞粘附分子超家族(IgCAMs)的一个包含六个成员的亚组,在大脑中表达显著且具有重要功能。最近针对神经精神疾病的遗传学研究已将接触蛋白4(CNTN4)、接触蛋白5(CNTN5)和接触蛋白6(CNTN6)确定为神经发育障碍的候选基因,尤其是在自闭症谱系障碍(ASD)中,同时在智力障碍、精神分裂症(SCZ)、注意力缺陷多动障碍(ADHD)、双相情感障碍(BD)、酒精使用障碍(AUD)和神经性厌食症(AN)中也是如此。这表明它们在神经发育过程中具有重要功能。有数据显示这些基因的破坏会影响神经突生长、细胞存活和神经回路形成,这支持了上述观点。在此,我们综述了有关它们参与神经精神疾病的当前遗传学数据,并探讨了关于无效突变如何影响小鼠行为的研究。最后,我们强调了蛋白质 - 蛋白质相互作用在Cntn4、-5和-6潜在作用机制中的作用,并强调与其他膜蛋白形成的复合物可能在神经元发育功能中发挥作用。

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