Departament de Genètica, Microbiologia i Estadística, Facultat de Biologia, Universitat de Barcelona, Barcelona, Catalonia, Spain; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III, Spain; Institut de Biomedicina de la Universitat de Barcelona (IBUB), Barcelona, Catalonia, Spain; Institut de Recerca Sant Joan de Déu (IR-SJD), Esplugues de Llobregat, Catalonia, Spain.
Department of Psychiatry and Psychotherapy, Central Institute of Mental Health, Medical Faculty Mannheim/Heidelberg University, Mannheim, Germany.
Eur Neuropsychopharmacol. 2020 Jan;30:44-55. doi: 10.1016/j.euroneuro.2017.11.012. Epub 2017 Nov 23.
The RBFOX1 gene (or A2BP1) encodes a splicing factor important for neuronal development that has been related to autism spectrum disorder and other neurodevelopmental phenotypes. Evidence from complementary sources suggests that this gene contributes to aggressive behavior. Suggestive associations with RBFOX1 have been identified in genome-wide association studies (GWAS) of anger, conduct disorder, and aggressive behavior. Nominal association signals in RBFOX1 were also found in an epigenome-wide association study (EWAS) of aggressive behavior. Also, variants in this gene affect temporal lobe volume, a brain area that is altered in several aggression-related phenotypes. In animals, this gene has been shown to modulate aggressive behavior in Drosophila. RBFOX1 has also been associated with canine aggression and is upregulated in mice that show increased aggression after frustration of an expected reward. Associated common genetic variants as well as rare duplications and deletions affecting RBFOX1 have been identified in several psychiatric and neurodevelopmental disorders that are often comorbid with aggressive behaviors. In this paper, we comprehensively review the cumulative evidence linking RBFOX1 to aggression behavior and provide new results implicating RBFOX1 in this phenotype. Most of these studies (genetic and epigenetic analyses in humans, neuroimaging genetics, gene expression and animal models) are hypothesis-free, which strengthens the validity of the findings, although all the evidence is nominal and should therefore be taken with caution. Further studies are required to clarify in detail the role of this gene in this complex phenotype.
RBFOX1 基因(或 A2BP1)编码一种对神经元发育很重要的剪接因子,与自闭症谱系障碍和其他神经发育表型有关。来自补充来源的证据表明,该基因与攻击行为有关。全基因组关联研究(GWAS)发现了与 RBFOX1 相关的提示性关联,在攻击性行为的全基因组关联研究(EWAS)中也发现了 RBFOX1 的名义关联信号。此外,该基因的变异影响颞叶体积,颞叶是与攻击行为相关表型改变的脑区。在动物中,该基因已被证明可以调节果蝇的攻击行为。RBFOX1 也与犬类攻击行为有关,在预期奖励受挫后表现出攻击性增加的小鼠中,该基因的表达上调。在几种常与攻击行为共病的精神和神经发育障碍中,已经发现了影响 RBFOX1 的常见遗传变异体以及罕见的重复和缺失。在本文中,我们全面综述了将 RBFOX1 与攻击行为联系起来的累积证据,并提供了新的结果,表明 RBFOX1 与这种表型有关。这些研究(人类的遗传和表观遗传分析、神经影像学遗传学、基因表达和动物模型)大多是无假设的,这增强了研究结果的有效性,尽管所有的证据都是名义上的,因此应该谨慎对待。需要进一步的研究来详细阐明该基因在这种复杂表型中的作用。