Literature DB >> 18379869

Behavioural analysis of congenic mouse strains confirms stress-responsive Loci on chromosomes 1 and 12.

M C Jawahar1, T C Brodnicki, F Quirk, Y M Wilson, M Murphy.   

Abstract

The way in which animals respond to stressful environments correlates with anxiety-related behaviour. To begin identifying the genetic factors that influence anxiety, we have studied the stress-responsiveness of inbred mouse strains using a modified form of the open field activity test (OFA), termed the elevated (e) OFA. In particular, two strains show high (DBA/2J) or low (C57BL/6J) stress-responsiveness in the eOFA. Genetic studies of an F(2) intercross between these two strains previously identified two regions, on chromosomes (Chr) 1 and 12, linked to anxiety-related behaviour. To confirm that these regions contain loci for stress-responsiveness, we established separate congenic mouse strains for the linked Chr1 and Chr12 regions. Each congenic strain harbours a DBA/2J-derived interval encompassing the linked region on the C57BL/6J genetic background: the congenic intervals are between, but not including approximately 48.6 Mb and approximately 194.8 Mb on Chr1, and approximately 36.2 Mb and the distal end of Chr12. Cohorts of DBA/2J, C57BL/6J and congenic mice were analysed for a series of stress-responsive phenotypes using the eOFA test. Both congenic strains had significantly different stress-responsive phenotypes compared to the low-stress C57BL/6J parental strain, but the DBA/2J-derived Chr12 interval had a greater genetic effect than the DBA/2J-derived Chr1 interval for changing the behavioral phenotype of the parental C57BL/6J mouse strain. These results confirmed the presence of stress-responsive loci on Chr1 and Chr12. New stress-related phenotypes were also identified, which aided in comparing and differentiating DBA/2J, C57BL/6J and congenic mice.

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Year:  2008        PMID: 18379869     DOI: 10.1007/s10519-008-9206-3

Source DB:  PubMed          Journal:  Behav Genet        ISSN: 0001-8244            Impact factor:   2.805


  4 in total

1.  Experimental sleep fragmentation and sleep deprivation in rats increases exploration in an open field test of anxiety while increasing plasma corticosterone levels.

Authors:  Jaime L Tartar; Christopher P Ward; Joshua W Cordeira; Steven L Legare; Amy J Blanchette; Robert W McCarley; Robert E Strecker
Journal:  Behav Brain Res       Date:  2008-09-02       Impact factor: 3.332

2.  Audiogenic seizure proneness requires the contribution of two susceptibility loci in mice.

Authors:  M Catharine Jawahar; Carolina I Sari; Yvette M Wilson; Andrew J Lawrence; Thomas Brodnicki; Mark Murphy
Journal:  Neurogenetics       Date:  2011-06-18       Impact factor: 2.660

3.  Melanopsin-expressing retinal ganglion cell loss and behavioral analysis in the Thy1-CFP-DBA/2J mouse model of glaucoma.

Authors:  Qi Zhang; Helen Vuong; Xin Huang; YanLing Wang; Nicholas C Brecha; MingLiang Pu; Jie Gao
Journal:  Sci China Life Sci       Date:  2013-06-01       Impact factor: 6.038

4.  The β-Secretase Substrate Seizure 6-Like Protein (SEZ6L) Controls Motor Functions in Mice.

Authors:  Emma Ong-Pålsson; Jasenka Rudan Njavro; Yvette Wilson; Martina Pigoni; Andree Schmidt; Stephan A Müller; Michael Meyer; Jana Hartmann; Marc Aurel Busche; Jenny M Gunnersen; Kathryn M Munro; Stefan F Lichtenthaler
Journal:  Mol Neurobiol       Date:  2021-12-27       Impact factor: 5.590

  4 in total

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