TY - JOUR
T1 - Brains, Genes, and Primates
AU - Izpisua Belmonte, Juan Carlos
AU - Callaway, Edward M.
AU - Churchland, Patricia
AU - Caddick, Sarah J.
AU - Feng, Guoping
AU - Homanics, Gregg E.
AU - Lee, Kuo Fen
AU - Leopold, David A.
AU - Miller, Cory T.
AU - Mitchell, Jude F.
AU - Mitalipov, Shoukhrat
AU - Moutri, Alysson R.
AU - Movshon, J. Anthony
AU - Okano, Hideyuki
AU - Reynolds, John H.
AU - Ringach, Dario
AU - Sejnowski, Terrence J.
AU - Silva, Afonso C.
AU - Strick, Peter L.
AU - Wu, Jun
AU - Zhang, Feng
N1 - Publisher Copyright:
© 2015 Elsevier Inc.
PY - 2015/5/6
Y1 - 2015/5/6
N2 - One of the great strengths of the mouse model is the wide array of genetic tools that have been developed. Striking examples include methods for directed modification of the genome, and for regulated expression or inactivation of genes. Within neuroscience, it is now routine to express reporter genes, neuronal activity indicators, and opsins in specific neuronal types in the mouse. However, there are considerable anatomical, physiological, cognitive, and behavioral differences between the mouse and the human that, in some areas of inquiry, limit the degree to which insights derived from the mouse can be applied to understanding human neurobiology. Several recent advances have now brought into reach the goal of applying these tools to understanding the primate brain. Here we describe these advances, consider their potential to advance our understanding of the human brain and brain disorders, discuss bioethical considerations, and describe what will be needed to move forward. Recent advances have brought into reach the goal of applying genetic tools to understanding the primate brain. Reynolds and colleagues describe these advances, their potential to deepen understanding of the human brain, and what will be needed to move forward.
AB - One of the great strengths of the mouse model is the wide array of genetic tools that have been developed. Striking examples include methods for directed modification of the genome, and for regulated expression or inactivation of genes. Within neuroscience, it is now routine to express reporter genes, neuronal activity indicators, and opsins in specific neuronal types in the mouse. However, there are considerable anatomical, physiological, cognitive, and behavioral differences between the mouse and the human that, in some areas of inquiry, limit the degree to which insights derived from the mouse can be applied to understanding human neurobiology. Several recent advances have now brought into reach the goal of applying these tools to understanding the primate brain. Here we describe these advances, consider their potential to advance our understanding of the human brain and brain disorders, discuss bioethical considerations, and describe what will be needed to move forward. Recent advances have brought into reach the goal of applying genetic tools to understanding the primate brain. Reynolds and colleagues describe these advances, their potential to deepen understanding of the human brain, and what will be needed to move forward.
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U2 - 10.1016/j.neuron.2015.03.021
DO - 10.1016/j.neuron.2015.03.021
M3 - Review article
C2 - 25950631
AN - SCOPUS:84928963567
SN - 0896-6273
VL - 86
SP - 617
EP - 631
JO - Neuron
JF - Neuron
IS - 3
ER -