A new locus regulating MICALL2 expression was identified for association with executive inhibition in children with attention deficit hyperactivity disorder.

作者: L Yang , S Chang , Q Lu , Y Zhang , Z Wu

DOI: 10.1038/MP.2017.74

关键词:

摘要: Impaired executive inhibition is a core deficit of attention hyperactivity disorder (ADHD), which common childhood-onset psychiatric with high heritability. In this study, we performed two-stage genome-wide association study in ADHD Han Chinese. We used the Stroop color-word interference test to evaluate inhibition. After quality control, 780 samples phenotype and covariate data were included discovery stage, whereas 922 replication stage. identified one new significant locus at 7p22.3 for word time (rs11514810, P=3.42E-09 discovery, P=0.01176 combined P=5.249E-09). Regulatory feature analysis expression quantitative trait loci (eQTL) showed that contributes MICALL2 human brain. Most genes network interacting associated disorders. Furthermore, hyperactive-impulsive-like behavior was induced by reducing zebrafish gene homologous MICALL2, could be rescued tomoxetine (atomoxetine), clinical medication ADHD. Our results suggested susceptibility deficiency related hyperactive-impulsive ADHD, further emphasizing possible role neurodevelopmental pathogenic mechanism

参考文章(60)
Noriyuki Nishimura, Takuya Sasaki, Cell-surface biotinylation to study endocytosis and recycling of occludin. Methods of Molecular Biology. ,vol. 440, pp. 89- 96 ,(2008) , 10.1007/978-1-59745-178-9_7
Noriyuki Nishimura, Takuya Sasaki, Identification and Characterization of JRAB/MICAL-L2, a Junctional Rab13-Binding Protein Methods in Enzymology. ,vol. 438, pp. 141- 153 ,(2008) , 10.1016/S0076-6879(07)38010-5
Valentina Mione, Sonia Canterini, Emiliano Brunamonti, Pierpaolo Pani, Federica Donno, Maria Teresa Fiorenza, Stefano Ferraina, Both the COMT Val158Met single-nucleotide polymorphism and sex-dependent differences influence response inhibition Frontiers in Behavioral Neuroscience. ,vol. 9, pp. 127- 127 ,(2015) , 10.3389/FNBEH.2015.00127
Stephanie H.M. Goozen, Kate Langley, Clare Northover, Kelly Hubble, Katya Rubia, Karen Schepman, Michael C. O'Donovan, Anita Thapar, Identifying mechanisms that underlie links between COMT genotype and aggression in male adolescents with ADHD Journal of Child Psychology and Psychiatry. ,vol. 57, pp. 472- 480 ,(2016) , 10.1111/JCPP.12464
Dirk Beuchle, Heinz Schwarz, Maria Langegger, Iris Koch, Hermann Aberle, Drosophila MICAL regulates myofilament organization and synaptic structure Mechanisms of Development. ,vol. 124, pp. 390- 406 ,(2007) , 10.1016/J.MOD.2007.01.006
Yongzhe Li, Kunlin Zhang, Hua Chen, Fei Sun, Juanjuan Xu, Ziyan Wu, Ping Li, Liuyan Zhang, Yang Du, Haixia Luan, Xi Li, Lijun Wu, Hongbin Li, Huaxiang Wu, Xiangpei Li, Xiaomei Li, Xiao Zhang, Lu Gong, Lie Dai, Lingyun Sun, Xiaoxia Zuo, Jianhua Xu, Huiping Gong, Zhijun Li, Shengquan Tong, Min Wu, Xiaofeng Li, Weiguo Xiao, Guochun Wang, Ping Zhu, Min Shen, Shengyun Liu, Dongbao Zhao, Wei Liu, Yi Wang, Cibo Huang, Quan Jiang, Guijian Liu, Bin Liu, Shaoxian Hu, Wen Zhang, Zhuoli Zhang, Xin You, Mengtao Li, Weixin Hao, Cheng Zhao, Xiaomei Leng, Liqi Bi, Yongfu Wang, Fengxiao Zhang, Qun Shi, Wencheng Qi, Xuewu Zhang, Yuan Jia, Jinmei Su, Qin Li, Yong Hou, Qingjun Wu, Dong Xu, Wenjie Zheng, Miaojia Zhang, Qian Wang, Yunyun Fei, Xuan Zhang, Jing Li, Ying Jiang, Xinping Tian, Lidan Zhao, Li Wang, Bin Zhou, Yang Li, Yan Zhao, Xiaofeng Zeng, Jurg Ott, Jing Wang, Fengchun Zhang, A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjögren's syndrome at 7q11.23 Nature Genetics. ,vol. 45, pp. 1361- 1365 ,(2013) , 10.1038/NG.2779
David Warde-Farley, Sylva L. Donaldson, Ovi Comes, Khalid Zuberi, Rashad Badrawi, Pauline Chao, Max Franz, Chris Grouios, Farzana Kazi, Christian Tannus Lopes, Anson Maitland, Sara Mostafavi, Jason Montojo, Quentin Shao, George Wright, Gary D. Bader, Quaid Morris, The GeneMANIA prediction server: biological network integration for gene prioritization and predicting gene function. Nucleic Acids Research. ,vol. 38, pp. 214- 220 ,(2010) , 10.1093/NAR/GKQ537