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MECP2 Duplication Causes Aberrant GABA Pathways, Circuits and Behaviors in Transgenic Monkeys: Neural Mappings to Patients with Autism.
Cai, Dan-Chao; Wang, Zhiwei; Bo, Tingting; Yan, Shengyao; Liu, Yilin; Liu, Zhaowen; Zeljic, Kristina; Chen, Xiaoyu; Zhan, Yafeng; Xu, Xiu; Du, Yasong; Wang, Yingwei; Cang, Jing; Wang, Guang-Zhong; Zhang, Jie; Sun, Qiang; Qiu, Zilong; Ge, Shengjin; Ye, Zheng; Wang, Zheng.
Afiliação
  • Cai DC; Institute of Neuroscience, CAS Center for Excellence in Brain Science and Intelligence Technology, State Key Laboratory of Neuroscience, CAS Key Laboratory of Primate Neurobiology, Chinese Academy of Sciences, Shanghai 200031, People's Republic of China.
  • Wang Z; Institute of Neuroscience, CAS Center for Excellence in Brain Science and Intelligence Technology, State Key Laboratory of Neuroscience, CAS Key Laboratory of Primate Neurobiology, Chinese Academy of Sciences, Shanghai 200031, People's Republic of China.
  • Bo T; University of Chinese Academy of Sciences, Shanghai 200031, People's Republic of China.
  • Yan S; Institute of Neuroscience, CAS Center for Excellence in Brain Science and Intelligence Technology, State Key Laboratory of Neuroscience, CAS Key Laboratory of Primate Neurobiology, Chinese Academy of Sciences, Shanghai 200031, People's Republic of China.
  • Liu Y; University of Chinese Academy of Sciences, Shanghai 200031, People's Republic of China.
  • Liu Z; Institute of Neuroscience, CAS Center for Excellence in Brain Science and Intelligence Technology, State Key Laboratory of Neuroscience, CAS Key Laboratory of Primate Neurobiology, Chinese Academy of Sciences, Shanghai 200031, People's Republic of China.
  • Zeljic K; University of Chinese Academy of Sciences, Shanghai 200031, People's Republic of China.
  • Chen X; Institute of Neuroscience, CAS Center for Excellence in Brain Science and Intelligence Technology, State Key Laboratory of Neuroscience, CAS Key Laboratory of Primate Neurobiology, Chinese Academy of Sciences, Shanghai 200031, People's Republic of China.
  • Zhan Y; University of Chinese Academy of Sciences, Shanghai 200031, People's Republic of China.
  • Xu X; Life Science Research Center, Engineering Research Center of Molecular and Neuro Imaging of Ministry of Education, School of Life Science and Technology, Xidian University, Xi'an 710126, People's Republic of China.
  • Du Y; Institute of Science and Technology for Brain Inspired Intelligence, Key Laboratory of Computational Neuroscience and Brain Inspired Intelligence, Fudan University, Shanghai 200433, People's Republic of China.
  • Wang Y; Institute of Neuroscience, CAS Center for Excellence in Brain Science and Intelligence Technology, State Key Laboratory of Neuroscience, CAS Key Laboratory of Primate Neurobiology, Chinese Academy of Sciences, Shanghai 200031, People's Republic of China.
  • Cang J; University of Chinese Academy of Sciences, Shanghai 200031, People's Republic of China.
  • Wang GZ; Institute of Neuroscience, CAS Center for Excellence in Brain Science and Intelligence Technology, State Key Laboratory of Neuroscience, CAS Key Laboratory of Primate Neurobiology, Chinese Academy of Sciences, Shanghai 200031, People's Republic of China.
  • Zhang J; University of Chinese Academy of Sciences, Shanghai 200031, People's Republic of China.
  • Sun Q; Institute of Neuroscience, CAS Center for Excellence in Brain Science and Intelligence Technology, State Key Laboratory of Neuroscience, CAS Key Laboratory of Primate Neurobiology, Chinese Academy of Sciences, Shanghai 200031, People's Republic of China.
  • Qiu Z; University of Chinese Academy of Sciences, Shanghai 200031, People's Republic of China.
  • Ge S; Department of Child Healthcare, Children's Hospital of Fudan University, Shanghai 201102, People's Republic of China.
  • Ye Z; Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai 200030, People's Republic of China.
  • Wang Z; Department of Anesthesiology, Huashan Hospital of Fudan University, Shanghai 200040, People's Republic of China.
J Neurosci ; 40(19): 3799-3814, 2020 05 06.
Article em En | MEDLINE | ID: mdl-32269107
ABSTRACT
MECP2 gain-of-function and loss-of-function in genetically engineered monkeys recapitulates typical phenotypes in patients with autism, yet where MECP2 mutation affects the monkey brain and whether/how it relates to autism pathology remain unknown. Here we report a combination of gene-circuit-behavior analyses including MECP2 coexpression network, locomotive and cognitive behaviors, and EEG and fMRI findings in 5 MECP2 overexpressed monkeys (Macaca fascicularis; 3 females) and 20 wild-type monkeys (Macaca fascicularis; 11 females). Whole-genome expression analysis revealed MECP2 coexpressed genes significantly enriched in GABA-related signaling pathways, whereby reduced ß-synchronization within fronto-parieto-occipital networks was associated with abnormal locomotive behaviors. Meanwhile, MECP2-induced hyperconnectivity in prefrontal and cingulate networks accounted for regressive deficits in reversal learning tasks. Furthermore, we stratified a cohort of 49 patients with autism and 72 healthy controls of 1112 subjects using functional connectivity patterns, and identified dysconnectivity profiles similar to those in monkeys. By establishing a circuit-based construct link between genetically defined models and stratified patients, these results pave new avenues to deconstruct clinical heterogeneity and advance accurate diagnosis in psychiatric disorders.SIGNIFICANCE STATEMENT Autism spectrum disorder (ASD) is a complex disorder with co-occurring symptoms caused by multiple genetic variations and brain circuit abnormalities. To dissect the gene-circuit-behavior causal chain underlying ASD, animal models are established by manipulating causative genes such as MECP2 However, it is unknown whether such models have captured any circuit-level pathology in ASD patients, as demonstrated by human brain imaging studies. Here, we use transgenic macaques to examine the causal effect of MECP2 overexpression on gene coexpression, brain circuits, and behaviors. For the first time, we demonstrate that the circuit abnormalities linked to MECP2 and autism-like traits in the monkeys can be mapped to a homogeneous ASD subgroup, thereby offering a new strategy to deconstruct clinical heterogeneity in ASD.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encéfalo / Proteína 2 de Ligação a Metil-CpG / Transtorno do Espectro Autista / Locomoção / Vias Neurais Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Animals / Female / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encéfalo / Proteína 2 de Ligação a Metil-CpG / Transtorno do Espectro Autista / Locomoção / Vias Neurais Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Animals / Female / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article