Targeted inactivation of the insulin receptor gene in mouse 3T3-L1 fibroblasts via homologous recombination

Proc Natl Acad Sci U S A. 1991 Jun 1;88(11):4708-12. doi: 10.1073/pnas.88.11.4708.

Abstract

To study the role of the insulin receptor in determining adipocyte differentiation of the mouse cell line 3T3-L1, we have introduced a mutation that inactivates the insulin receptor gene by homologous recombination. In two independent clones, inactivation of one allele of the insulin receptor gene was associated with a 50-70% reduction in the number of insulin receptors. In addition, both clones were markedly impaired in their ability to differentiate into adipocytes. The defect in adipocyte-specific differentiation was corrected by expression of transfected human insulin receptor cDNA. These data suggest that the insulin receptor may play an important role in promoting differentiation of 3T3-L1 cells into adipocytes in vitro.

MeSH terms

  • Animals
  • Base Sequence
  • Blotting, Southern
  • Cell Differentiation
  • Cell Line
  • DNA / genetics
  • DNA / isolation & purification
  • Gene Expression Regulation
  • Gene Rearrangement
  • Genetic Vectors
  • Humans
  • L Cells / cytology
  • L Cells / physiology
  • Mice
  • Molecular Sequence Data
  • Oligonucleotide Probes
  • RNA, Messenger / genetics
  • Receptor, Insulin / genetics*
  • Recombination, Genetic*
  • Restriction Mapping
  • Transfection

Substances

  • Oligonucleotide Probes
  • RNA, Messenger
  • DNA
  • Receptor, Insulin