Sakamoto Kensuke, Crowley James J
Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
Am J Med Genet B Neuropsychiatr Genet. 2018 Mar;177(2):242-256. doi: 10.1002/ajmg.b.32554. Epub 2017 Jun 14.
Since it was first associated with schizophrenia (SCZ) in a 2011 genome-wide association study (GWAS), there have been over 100 publications focused on MIR137, the gene encoding microRNA-137. These studies have examined everything from its fundamental role in the development of mice, flies, and fish to the intriguing enrichment of its target gene network in SCZ. Indeed, much of the excitement surrounding MIR137 is due to the distinct possibility that it could regulate a gene network involved in SCZ etiology, a disease which we now recognize is highly polygenic. Here we comprehensively review, to the best of our ability, all published genetic and biological evidence that could support or refute a role for MIR137 in the etiology of SCZ. Through a careful consideration of the literature, we conclude that the data gathered to date continues to strongly support the involvement of MIR137 and its target gene network in neuropsychiatric traits, including SCZ risk. There remain, however, more unanswered than answered questions regarding the mechanisms linking MIR137 genetic variation with behavior. These questions need answers before we can determine whether there are opportunities for diagnostic or therapeutic interventions based on MIR137. We conclude with a number of suggestions for future research on MIR137 that could help to provide answers and hope for a greater understanding of this devastating disorder.
自2011年全基因组关联研究(GWAS)首次将其与精神分裂症(SCZ)联系起来后,已有100多篇论文聚焦于编码微小RNA - 137的基因MIR137。这些研究涵盖了从其在小鼠、果蝇和鱼类发育中的基本作用,到其靶基因网络在精神分裂症中有趣的富集情况等方方面面。事实上,围绕MIR137的诸多兴奋点在于,它极有可能调控一个与精神分裂症病因相关的基因网络,而我们现在认识到精神分裂症是一种高度多基因的疾病。在此,我们尽最大能力全面回顾了所有已发表的、能支持或反驳MIR137在精神分裂症病因中作用的遗传和生物学证据。通过仔细研读文献,我们得出结论,迄今收集到的数据继续有力支持MIR137及其靶基因网络参与神经精神性状,包括精神分裂症风险。然而,关于将MIR137基因变异与行为联系起来的机制,未解之谜仍多于已解答的问题。在我们能够确定是否有基于MIR137进行诊断或治疗干预的机会之前,这些问题需要得到解答。我们最后针对MIR137未来的研究提出了一些建议,这些研究可能有助于提供答案,并有望更深入地了解这种毁灭性疾病。