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Generation of Genetically Engineered Non-human Primate Models of Brain Function and Neurological Disorders

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Journal Am J Primatol
Date 2018 Dec 27
PMID 30585654
Citations 16
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Abstract

Research with non-human primates (NHP) has been essential and effective in increasing our ability to find cures for a large number of diseases that cause human suffering and death. Extending the availability and use of genetic engineering techniques to NHP will allow the creation and study of NHP models of human disease, as well as broaden our understanding of neural circuits in the primate brain. With the recent development of efficient genetic engineering techniques that can be used for NHP, there's increased hope that NHP will significantly accelerate our understanding of the etiology of human neurological and neuropsychiatric disorders. In this article, we review the present state of genetic engineering tools used in NHP, from the early efforts to induce exogeneous gene expression in macaques and marmosets, to the latest results in producing germline transmission of different transgenes and the establishment of knockout lines of specific genes. We conclude with future perspectives on the further development and employment of these tools to generate genetically engineered NHP.

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References
1.
Gaudelli N, Komor A, Rees H, Packer M, Badran A, Bryson D . Programmable base editing of A•T to G•C in genomic DNA without DNA cleavage. Nature. 2017; 551(7681):464-471. PMC: 5726555. DOI: 10.1038/nature24644. View

2.
Tan W, Proudfoot C, Lillico S, Whitelaw C . Gene targeting, genome editing: from Dolly to editors. Transgenic Res. 2016; 25(3):273-87. PMC: 4882362. DOI: 10.1007/s11248-016-9932-x. View

3.
Chen Y, Niu Y, Li Y, Ai Z, Kang Y, Shi H . Generation of Cynomolgus Monkey Chimeric Fetuses using Embryonic Stem Cells. Cell Stem Cell. 2015; 17(1):116-24. DOI: 10.1016/j.stem.2015.06.004. View

4.
Moran S, Chi T, Prucha M, Ahn K, Connor-Stroud F, Jean S . Germline transmission in transgenic Huntington's disease monkeys. Theriogenology. 2015; 84(2):277-85. PMC: 4631054. DOI: 10.1016/j.theriogenology.2015.03.016. View

5.
Bak R, Gomez-Ospina N, Porteus M . Gene Editing on Center Stage. Trends Genet. 2018; 34(8):600-611. DOI: 10.1016/j.tig.2018.05.004. View