Motor coordination deficits in Alpk1 mutant mice with the inserted piggyBac transposon

BMC Neurosci. 2011 Jan 5;12:1. doi: 10.1186/1471-2202-12-1.


Background: ALPK1 (α-kinase 1) is a member of an unconventional alpha-kinase family, and its biological function remains largely unknown. Here we report the phenotypic characterization of one mutant line, in which the piggyBac (PB) transposon is inserted into the Alpk1 gene.

Results: The piggyBac(PB) insertion site in mutants was mapped to the first intron of the Alpk1 gene, resulting in the effective disruption of the intact Alpk1 transcript expression. The transposon-inserted Alpk1 homozygous mutants (Alpk1PB/PB) displayed severe defects in motor coordination in a series of behavioral analysis, including dowel test, hanging wire test, rotarod analysis and footprint analysis. However, the cerebellar architecture, Purkinje cell morphology and electrophysiology of the Purkinje cells appeared normal in mutants. The motor coordination deficits in the Alpk1PB/PB mice were rescued by transgenic mice expressing the full-length Alpk1-coding sequence under the control of the ubiquitous expression promoter.

Conclusions: Our results indicate that ALPK1 plays an important role in the regulation of motor coordination. Alpk1PB/PB mice would be a useful model to provide a clue to the better understanding of the cellular and molecular mechanisms of ALPK1 in the control of fine motor activities.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcium-Calmodulin-Dependent Protein Kinases / genetics*
  • Chromosomes, Artificial, Bacterial / genetics*
  • DNA Transposable Elements / genetics*
  • Male
  • Mice
  • Mice, Transgenic
  • Motor Skills Disorders / enzymology*
  • Motor Skills Disorders / genetics*
  • Motor Skills Disorders / pathology
  • Mutagenesis, Insertional / methods*
  • Mutation / genetics*


  • DNA Transposable Elements
  • Calcium-Calmodulin-Dependent Protein Kinases