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Comprehensive behavioral phenotyping of calpastatin-knockout mice

Ryuichi Nakajima1,5 email, Keizo Takao2,3,4 email, Shu-Ming Huang1,6 email, Jiro Takano1 email, Nobuhisa Iwata1 email, Tsuyoshi Miyakawa2,3,4 email and Takaomi C Saido1 email

Laboratory for Proteolytic Neuroscience, RIKEN Brain Science Institute, Saitama, Japan

Genetic Engineering and Functional Genomics Group, Frontier Technology Center, Graduate School of Medicine, Kyoto University, Kyoto, Japan

Division of Systems Medicine, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Japan

JST, CREST, Hon-chou, Kawaguchi, Saitama, Japan

Current Address: Department of Physiology & Biophysics, Dalhousie University Faculty of Medicine, Halifax, Nova Scotia, Canada

Current Address: Department of Neuroscience, Institute for Chinese Medicine, Heilongjiang University of Chinese Medicine, Harbin, PR China

author email corresponding author email

Molecular Brain 2008, 1:7doi:10.1186/1756-6606-1-7

Published: 15 September 2008

Additional files

Additional file 1:

Crawley's Sociability and social novelty preference test. We could not detect any significant difference between genotypes in exploratory behavior within either the first trial with one stranger mouse (F1,34 = 1.496, P = 0.2297 in the empty side; F1,34 = 0.242, P = 0.6256 in the stranger side; A), nor the following trial with an additional stranger mouse (F1,34 = 0.797, P = 0.3781 in the stranger 1 side; F1,34 = 0.105, P = 0.7483 in the stranger 2 side; B). The colors of mice in A and B, and the colors of lines under the bar graphs are corresponding to each other (white: empty side, light gray: stranger 1 side, dark gray: stranger 2 side).

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Additional file 2:

Social interaction in home cage. Social interactions in home cage were normal in clustering (F1,17 = 0.54, P = 0.820; A). Activity level was not significantly different between genotypes either (F1,17 = 0.38, P = 0.547; B).

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Additional file 3:

Light and dark transition test. CS-KO mice showed no significant differences in the light/dark transition test in distance traveled (F1,36 = 0.011, P = 0.917 in light camber, F1,36 = 0.293, P = 0.592 in the dark chamber; Aa), in stay time in the light chamber (F1,36 = 0.158, P = 0.694; Ab), in the number of transitions (F1,36 = 0.448, P = 0.508; Ac), or in latency to first entry into the light chamber (F1,36 = 0.006, P = 0.936; Figure Ad).

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Additional file 4:

Comparison of mRNA expression levels of μ-calpain, m-calpain and calpastatin. Using Allen Brain Atlas, an in situ hybridization database of mouse brain, mRNA expression levels were compared among μ-calpain, m-calpain and calpastatin (Arranged to a bar chart by authors). Allen Brain Atlas [Internet]. Seattle (WA): Allen Institute for Brain Science. © 2008. Available from: http://www.brain-map.org webcite.

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