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Targeted ANP32E mutant mice do not demonstrate obvious movement defects.


ABSTRACT: BACKGROUND: The ANP32 family of proteins have been implicated in neuronal function through biochemical and cellular biology studies in neurons, as well as by recent behavioural studies of a gene-trapped loss-of-function mutation of Anp32e in mice, particularly with respect to fine motor function. A second targeted allele of the Anp32e, however, did not appear to demonstrate neurological phenotypes. METHODOLOGY/PRINCIPAL FINDINGS: Using a stringently controlled cohort of ten-generation backcrossed, co-caged, sex-matched, littermate pairs, we assayed for potential motor defects in the targeted ANP32E-deficient mice. We found no phenotypic difference in any assays. CONCLUSION: Since it is unlikely that the gene-trap is a more complete loss-of-function, our results suggest that ANP32E has no appreciable effect on motor functions and that genetic background differences most likely account for the gene-trap phenomena.

SUBMITTER: Wong P 

PROVIDER: S-EPMC3652840 | biostudies-literature | 2013

REPOSITORIES: biostudies-literature

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Targeted ANP32E mutant mice do not demonstrate obvious movement defects.

Wong Peiyan P   Leo Vonny I VI   Low Meijun M   Mak Tak W TW   Zhang Xiaodong X   Reilly Patrick T PT  

PloS one 20130513 5


<h4>Background</h4>The ANP32 family of proteins have been implicated in neuronal function through biochemical and cellular biology studies in neurons, as well as by recent behavioural studies of a gene-trapped loss-of-function mutation of Anp32e in mice, particularly with respect to fine motor function. A second targeted allele of the Anp32e, however, did not appear to demonstrate neurological phenotypes.<h4>Methodology/principal findings</h4>Using a stringently controlled cohort of ten-generati  ...[more]

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