Effect of the rd1 mutation on motor performance in R6/2 and wild type mice

• Published in: PLoS currents 2012-02, Vol.4, p.RRN1303-RRN1303
• Main Authors: Menalled, Liliana, El-Khodor, Bassem F, Hornberger, Monica, Park, Larry, Howland, David, Brunner, Dani
• Format: Article
• Language: English
• Subjects: Huntington Disease
• ISSN: 2157-3999; 2157-3999
• DOI: 10.1371/currents.rrn1303

Homozygosis for the rd1 mutation in the Pbe6b gene results in the loss of the rod b-subunit of the cyclic GMP phosphodiesterase and, eventually, of all rod and cone photoreceptors. The R6/2 mouse line is a widely used model of Huntington's disorder (HD). The original line was made available on a mixed background obtained by crossing, via ovarian transplant, female R6/2 (on a B6CBA mixed background) with male B6CBAF1/J mice. As the CBA/J strain used in the US is homozygous for the rd1 mutation and the breeding scheme does not ensure heterozygosis for the mutation, a significant percentage of the offspring on this mixed background is expected to be homozygous for the rd1 mutation. We investigate here the effect of rd1 homozygosis on motor function and examined the effects of the mutation on the R6/2 phenotype. Homozygosis for the rd1 mutation resulted in increased activity in the open field test and reduced rotarod test performance. In addition, rd1 mutation absence or heterozygosis reduced the differences between the R6/2 and the WT mice. Our recommendation for the neurodegeneration field, and for all mouse studies in general, is to carefully control homozygosis for retinal degeneration mutation, even when using tests of motor function.