A Genetic Variant BDNF Polymorphism Alters Extinction Learning in Both Mouse and Human

Author:

Soliman Fatima12,Glatt Charles E.2,Bath Kevin G.2,Levita Liat12,Jones Rebecca M.12,Pattwell Siobhan S.2,Jing Deqiang2,Tottenham Nim12,Amso Dima12,Somerville Leah H.12,Voss Henning U.3,Glover Gary4,Ballon Douglas J.3,Liston Conor12,Teslovich Theresa12,Van Kempen Tracey12,Lee Francis S.2,Casey B. J.12

Affiliation:

1. The Sackler Institute for Developmental Psychobiology, Weill Cornell Medical College, New York, NY 10065, USA.

2. Department of Psychiatry, Weill Cornell Medical College, New York, NY 10065, USA.

3. Citigroup Biomedical Imaging Center, Department of Radiology, Weill Cornell Medical College, New York, NY 10065, USA.

4. Lucas Center for Imaging, Department of Radiology, Stanford University, Stanford, CA 94305, USA.

Abstract

Of Mice and Men Just how closely must mouse models replicate the known features of human disorders to be accepted as useful for mechanistic and therapeutic studies? Soliman et al. (p. 863 , published online 14 January) compared mice that vary only in their allelic composition at one position within the gene encoding brain-derived neurotrophic factor (BDNF) with humans exhibiting the same range of allelic variation. Individuals (mice and humans) carrying the allele that codes for a methionine-containing variant of BDNF retained a fearful response to a threatening stimulus even after its removal in comparison to those with the valine variant. Furthermore, in both cases, this linkage was mediated by diminished activity in the ventral-medial region of the prefrontal cortex. This deficit in extinction learning may contribute to differential responses to extinction-based therapies for anxiety disorders.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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