Generation of ES cells for conditional expression of nuclear receptors and coregulators in vivo

San-Pin Wu1, Dong-Kee Lee, Francesco J Demayo

  • 1Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas 77030, USA.

Insights

Researchers developed a conditional overexpression system in mouse embryonic stem cells for studying nuclear receptors and coregulators. This system, demonstrated with human chicken ovalbumin upstream promoter-transcription factor I (COUP-TFI), enables tissue-specific gene expression for disease research.

Area of Science:

  • Molecular Biology
  • Genetics
  • Developmental Biology

Background:

  • Nuclear receptors and coregulators are crucial for biological functions.
  • Dysregulation of these factors is linked to various human diseases.
  • A versatile tool for studying their roles is needed.

Purpose of the Study:

  • To establish a conditional overexpression system in mouse embryonic stem (ES) cells.
  • To enable spatial and temporal gene expression of nuclear receptors and coregulators.
  • To investigate the function and similarity of COUP-TFI and COUP-TFII.

Main Methods:

  • Development of a minigene system at the Rosa26 locus in mouse ES cells.
  • Utilized cre-lox recombination to control transgene expression.
  • Generated a CAG-S-hCOUP-TFI allele for conditional overexpression in mice.

Main Results:

  • The conditional overexpression system successfully expressed human chicken ovalbumin upstream promoter-transcription factor I (COUP-TFI) in various tissues.
  • COUP-TFI expression in COUP-TFII-deficient mice rescued uterine implantation and decidualization defects.
  • Demonstrated functional compensation between COUP-TFI and COUP-TFII in the uterus.

Conclusions:

  • The developed conditional overexpression system is a valuable resource for studying nuclear receptors and coregulators.
  • COUP-TFI and COUP-TFII exhibit functional similarity and can compensate for each other.
  • This system facilitates research into gene function and disease mechanisms.

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