Literature DB >> 17083330

FVB.129P2-Pde6b(+) Tyr(c-ch)/Ant, a sighted variant of the FVB/N mouse strain suitable for behavioral analysis.

V Errijgers1, D Van Dam, I Gantois, C J Van Ginneken, A W Grossman, R D'Hooge, P P De Deyn, R F Kooy.   

Abstract

Mice of the FVB/N strain are severely visual impaired as a result of tyrosinase gene defects, leading to a deficiency of the key enzyme for melanin synthesis in skin and eye and of cyclic guanosine monophosphate phosphodiesterase gene defects, which results in albinism (Tyr(c/c)) and retinal degeneration (Pde6b(rd1/rd1)), respectively. Nevertheless, FVB/N mice are commonly used for the generation of transgenic animals because of their large, strong pronuclei and high breeding performance. However, due to visual impairment of the FVB/N animals, the resulting transgenic animals cannot be used in tests that depend on vision, including tests of cognitive behavior. Therefore, we have bred a sighted version of the FVB/N strain by an outcross between FVB/N and 129P2/OlaHsd, followed by repeated backcrosses to FVB/N mice while selecting against albinism and homozygosity of the retinal degeneration mutation. After 11 generations of backcrossing, sighted animals were intercrossed to generate the congenic FVB.129P2-Pde6b(+) Tyr(c-ch)/Ant strain, which is pigmented (Tyr(c-ch)/(c-ch)) and devoid of the genetic predisposition to retinal degeneration. The accurate visual abilities of the FVB.129P2-Pde6b(+) Tyr(c-ch)/Ant mice, for which we propose the name FVBS/Ant, demonstrated a clear visual evoked potential in the presence of normal eye histology and improved performance in the Morris water maze test.

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Year:  2006        PMID: 17083330     DOI: 10.1111/j.1601-183X.2006.00282.x

Source DB:  PubMed          Journal:  Genes Brain Behav        ISSN: 1601-183X            Impact factor:   3.449


  25 in total

1.  Reevaluating hippocampus-dependent learning in FVB/N mice.

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Review 2.  The importance of considering all attributes of memory in behavioral endophenotyping of mouse models of genetic disease.

Authors:  Michael R Hunsaker
Journal:  Behav Neurosci       Date:  2012-06       Impact factor: 1.912

3.  Neuroanatomical analysis of the BTBR mouse model of autism using magnetic resonance imaging and diffusion tensor imaging.

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4.  Low sociability in BTBR T+tf/J mice is independent of partner strain.

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Journal:  Physiol Behav       Date:  2012-01-08

5.  Early social enrichment rescues adult behavioral and brain abnormalities in a mouse model of fragile X syndrome.

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Journal:  Neuropsychopharmacology       Date:  2015-03-13       Impact factor: 7.853

6.  Differences in memory development among C57BL/6NCrl, 129S2/SvPasCrl, and FVB/NCrl mice after delay and trace fear conditioning.

Authors:  Amelia March; David Borchelt; Todd Golde; Christopher Janus
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7.  Effects of stimulus salience on touchscreen serial reversal learning in a mouse model of fragile X syndrome.

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Journal:  Brain Behav Immun       Date:  2016-09-10       Impact factor: 7.217

9.  Rescue of fragile X syndrome phenotypes in Fmr1 KO mice by the small-molecule PAK inhibitor FRAX486.

Authors:  Bridget M Dolan; Sergio G Duron; David A Campbell; Benedikt Vollrath; B S Shankaranarayana Rao; Hui-Yeon Ko; Gregory G Lin; Arvind Govindarajan; Se-Young Choi; Susumu Tonegawa
Journal:  Proc Natl Acad Sci U S A       Date:  2013-03-18       Impact factor: 11.205

10.  Social approach in genetically engineered mouse lines relevant to autism.

Authors:  S S Moy; J J Nadler; N B Young; R J Nonneman; A W Grossman; D L Murphy; A J D'Ercole; J N Crawley; T R Magnuson; J M Lauder
Journal:  Genes Brain Behav       Date:  2008-11-11       Impact factor: 3.449

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