Motor deficits on a ladder rung task in male and female adolescent and adult CGG knock-in mice

MR Hunsaker, RE von Leden, BT Ta, NJ Goodrich-Hunsaker, G Argue, K Kim, Rob Willemsen, RF Berman

Research output: Contribution to journalArticleAcademicpeer-review

38 Citations (Scopus)

Abstract

The fragile X premutation is a tandem CGG trinucleotide repeat expansion on the FMR1 gene between 55 and 200 repeats in length. A CGG knock-in (CGG KI) mouse with CGG trinucleotide repeat lengths between 70 and 350 has been developed and used to model the histopathology and cognitive deficits reported in carriers of the fragile X premutation. Previous studies have shown that CGG KI mice show progressive deficits in processing spatial and temporal information. To characterize the motor deficits associated with the fragile X premutation, male and female CGG KI mice ranging from 2 to 16 months of age with trinucleotide repeats ranging from 72 to 240 CGG in length were tested for their ability to perform a skilled ladder rung walking test. The results demonstrate that both male and female CGG KI mice showed a greater number of foot slips as a function of increased CGG repeat length, independent of the age of the animal or general activity level. (C) 2011 Elsevier B.V. All rights reserved.
Original languageUndefined/Unknown
Pages (from-to)117-121
Number of pages5
JournalBehavioural Brain Research
Volume222
Issue number1
DOIs
Publication statusPublished - 2011

Research programs

  • EMC MGC-02-96-01

Cite this