A polymorphism in New Zealand inbred mouse strains that inactivates phosphatidylcholine transfer protein

FEBS Lett. 2006 Oct 30;580(25):5953-8. doi: 10.1016/j.febslet.2006.09.066. Epub 2006 Oct 6.

Abstract

New Zealand obese (NZO/HlLt) male mice develop polygenic diabetes and altered phosphatidylcholine metabolism. The gene encoding phosphatidylcholine transfer protein (PC-TP) is sited within the support interval for Nidd3, a recessive NZO-derived locus on Chromosome 11 identified by prior segregation analysis between NZO/HlLt and NON/Lt. Sequence analysis revealed that the NZO-derived PC-TP contained a non-synonymous point mutation that resulted in an Arg120His substitution, which was shared by the related NZB/BlNJ and NZW/LacJ mouse strains. Consistent with the structure-based predictions, functional studies demonstrated that Arg120His PC-TP was inactive, suggesting that this mutation contributes to the deficiencies in phosphatidylcholine metabolism observed in NZO mice.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Substitution
  • Animals
  • Base Sequence
  • Chromosome Mapping
  • DNA, Complementary / genetics
  • Male
  • Mice
  • Mice, Inbred NZB / genetics*
  • Mice, Inbred Strains
  • Mice, Obese / genetics*
  • Mice, Obese / metabolism
  • Models, Molecular
  • Phosphatidylcholines / metabolism
  • Phospholipid Transfer Proteins / antagonists & inhibitors*
  • Phospholipid Transfer Proteins / chemistry
  • Phospholipid Transfer Proteins / genetics*
  • Point Mutation
  • Polymorphism, Genetic*
  • Protein Conformation
  • Species Specificity

Substances

  • DNA, Complementary
  • Phosphatidylcholines
  • Phospholipid Transfer Proteins