CPD-1 null mice display a subtle neurological phenotype

Rupinder K. Kular, Rocky G. Gogliotti, Puneet Opal*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

6 Scopus citations


Background: CPD1 (also known as ANP32-E) belongs to a family of evolutionarily conserved acidic proteins with leucine rich repeats implicated in a variety of cellular processes regulating gene expression, vesicular trafficking, intracellular signaling and apoptosis. Because of its spatiotemporal expression pattern, CPD1 has been proposed to play an important role in brain morphogenesis and synaptic development. Methodology/Principal Findings: We have generated CPD1 knock-out mice that we have subsequently characterized. These mice are viable and fertile. However, they display a subtle neurological clasping phenotype and mild motor deficits. Conclusions/Significance: CPD1 is not essential for normal development; however, it appears to play a role in the regulation of fine motor functions. The minimal phenotype suggests compensatory biological mechanisms.

Original languageEnglish (US)
Article numbere12649
Pages (from-to)1-7
Number of pages7
JournalPloS one
Issue number9
StatePublished - 2010

ASJC Scopus subject areas

  • Agricultural and Biological Sciences(all)
  • General
  • Biochemistry, Genetics and Molecular Biology(all)


Dive into the research topics of 'CPD-1 null mice display a subtle neurological phenotype'. Together they form a unique fingerprint.

Cite this