Highly B lymphocyte-specific tamoxifen inducible transgene expression of CreER T2 by using the LC-1 locus BAC vector

Genesis. 2009 Nov;47(11):729-35. doi: 10.1002/dvg.20549.

Abstract

The generation of cell type specific inducible Cre transgenic mice is the most challenging and limiting part in the development of spatio-temporally controlled knockout mouse models. Here we report the generation and characterization of a B lymphocyte-specific tamoxifen-inducible Cre transgenic mouse strain, LC-1-hCD19-CreER(T2). We utilized the human CD19 promoter for expression of the tamoxifen-inducible Cre recombinase (CreER(T2)) gene, embedded in genomic sequences previously reported to give minimal position effects after transgenesis. Cre recombinase activity was evaluated by cross-breeding the LC-1-hCD19-CreER(T2) strain with a strain containing a floxed gene widely expressed in the hematopoietic system. Cre activity was only detected in the presence of tamoxifen and was restricted to B lymphocytes. The efficacy of recombination ranged from 27 to 61% in the hemizygous and homozygous mice, respectively. In conclusion, the LC-1-hCD19-CreER(T2) strain is a powerful tool to study gene function specifically in B lymphocytes at any chosen time point in the lifecycle of the mouse.

MeSH terms

  • Animals
  • Antigens, CD19 / genetics
  • B-Lymphocytes / metabolism*
  • Base Sequence
  • Chromosomes, Artificial, Bacterial*
  • DNA Primers
  • Gene Expression Regulation / drug effects*
  • Humans
  • Integrases / genetics*
  • Mice
  • Mice, Transgenic
  • Polymerase Chain Reaction
  • Tamoxifen / pharmacology*
  • Transgenes*

Substances

  • Antigens, CD19
  • DNA Primers
  • Tamoxifen
  • Cre recombinase
  • Integrases