中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Modeling Rett Syndrome Using TALEN-Edited MECP2 Mutant Cynomolgus Monkeys

文献类型:期刊论文

作者Chen, Yongchang1,3,14; Yu, Juehua2; Niu, Yuyu1,3,14; Qin, Dongdong5; Liu, Hailiang2; Li, Gang6,7; Hu, Yingzhou5; Wang, Jiaojian8; Lu, Yi9; Kang, Yu1,3,14
刊名CELL
出版日期2017-05-18
卷号169期号:5页码:945-+
DOI10.1016/j.cell.2017.04.035
文献子类Article
英文摘要Gene-editing technologies have made it feasible to create nonhuman primate models for human genetic disorders. Here, we report detailed genotypes and phenotypes of TALEN-edited MECP2 mutant cynomolgus monkeys serving as a model for a neurodevelopmental disorder, Rett syndrome (RTT), which is caused by loss-of-function mutations in the human MECP2 gene. Male mutant monkeys were embryonic lethal, reiterating that RTT is a disease of females. Through a battery of behavioral analyses, including primate-unique eye-tracking tests, in combination with brain imaging via MRI, we found a series of physiological, behavioral, and structural abnormalities resembling clinical manifestations of RTT. Moreover, blood transcriptome profiling revealed that mutant monkeys resembled RTT patients in immune gene dysregulation. Taken together, the stark similarity in phenotype and/or endophenotype between monkeys and patients suggested that gene-edited RTT founder monkeys would be of value for disease mechanistic studies as well as development of potential therapeutic interventions for RTT.
WOS关键词CPG-BINDING PROTEIN-2 ; NETWORK ANALYSIS ; MICE ; PRIMATES ; AUTISM ; GIRLS ; ABNORMALITIES ; NEUROANATOMY ; DEFICIENCY ; REGRESSION
WOS研究方向Biochemistry & Molecular Biology ; Cell Biology
语种英语
WOS记录号WOS:000401515900018
资助机构National Key Research and Development Program(2016YFA0101401 ; National & Provincial Natural Science Foundation of China(U1602224 ; National Institute of Child Health Development of the NIH(U54HD087101-01) ; 2016YFA0100800) ; U1302227 ; 31571534 ; 2015FA037 ; 91319309 ; 31450110428 ; 31620103904 ; 2013HB133 ; 13JC1407102)
源URL[http://ir.ia.ac.cn/handle/173211/15097]  
专题自动化研究所_脑网络组研究中心
作者单位1.Kunming Univ Sci & Technol, Inst Primate Translat Med, Yunnan Key Lab Primate Biomed Res, Kunming 650500, Peoples R China
2.Tongji Univ, Sch Med, Tongji Hosp, Translat Stem Cell Res Ctr, Shanghai 200065, Peoples R China
3.Yunnan Prov Acad Sci & Technol, Kunming 650051, Peoples R China
4.Univ Calif Los Angeles, Sch Med, Dept Psychiat & Biobehav Sci, Los Angeles, CA 90095 USA
5.Chinese Acad Sci, Kunming Inst Zool, Chinese Acad Sci & Yunnan Prov, Key Lab Anim Models & Human Dis Mech, Kunming 650223, Peoples R China
6.Univ North Carolina Chapel Hill, Dept Radiol, Chapel Hill, NC 27599 USA
7.Univ North Carolina Chapel Hill, BRIC, Chapel Hill, NC 27599 USA
8.Univ Elect Sci & Technol China, Sch Life Sci & Technol, Minist Educ, Key Lab NeuroInformat, Chengdu 625014, Peoples R China
9.Kunming Med Univ, Affiliated Hosp 1, Dept Med Imaging, Kunming 650032, Peoples R China
10.Kunming Univ Sci & Technol, Peoples Hosp Yunnan Prov 1, Kunming 650032, Peoples R China
推荐引用方式
GB/T 7714
Chen, Yongchang,Yu, Juehua,Niu, Yuyu,et al. Modeling Rett Syndrome Using TALEN-Edited MECP2 Mutant Cynomolgus Monkeys[J]. CELL,2017,169(5):945-+.
APA Chen, Yongchang.,Yu, Juehua.,Niu, Yuyu.,Qin, Dongdong.,Liu, Hailiang.,...&Sun, Yi Eve.(2017).Modeling Rett Syndrome Using TALEN-Edited MECP2 Mutant Cynomolgus Monkeys.CELL,169(5),945-+.
MLA Chen, Yongchang,et al."Modeling Rett Syndrome Using TALEN-Edited MECP2 Mutant Cynomolgus Monkeys".CELL 169.5(2017):945-+.

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来源:自动化研究所

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