Transgenic over-expression of MafK suppresses T cell proliferation and function in vivo

Genes Cells. 2001 Dec;6(12):1055-66. doi: 10.1046/j.1365-2443.2001.00489.x.

Abstract

Background: The small Maf proteins regulate gene transcription from Maf recognition elements (MARE). These proteins do not contain a canonical transactivation domain. Depending upon the ratio of small Maf proteins to their partner proteins, which either possess a transactivation domain or not, transcription can be switched on or off.

Results: Transgenic mice were generated which over-express the small Maf family member MafK, specifically in the T cell lineage. It was our expectation that the high level of MafK would shift the balance to the formation of MafK homodimer and thereby repress MARE-dependent transcription. The transgenic mice had a shortened life span because of Pneumocystis carinii pneumonia and displayed a decrease in thymocytes and lower IL-2 and IL-4 mRNA expression levels. Analyses by electrophoretic gel mobility shift assay revealed that over-expressed MafK could interact with the proximal AP-1 sequence of IL-2 and the MARE in the IL-4 promoter region.

Conclusion: These results indicate that when over-expressed, MafK binds to a MARE-like sequence and represses MARE-dependent transcription. Consequently, T cell proliferation and cytokine secretion are affected. The MafK homodimer serves as an important molecular probe for evaluating the role played by cis-acting MAREs in the proliferation and function of T cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Gene Expression Regulation*
  • Immunoglobulin G / blood
  • Interleukin-2 / metabolism
  • Interleukin-4 / metabolism
  • Lymphocyte Activation
  • MafK Transcription Factor
  • Mice
  • Mice, Transgenic
  • Nuclear Proteins / biosynthesis
  • Nuclear Proteins / genetics*
  • Pneumonia, Pneumocystis / etiology
  • Pneumonia, Pneumocystis / genetics
  • RNA, Messenger / biosynthesis
  • Reverse Transcriptase Polymerase Chain Reaction
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / metabolism*
  • Transcription Factor AP-1 / metabolism

Substances

  • Immunoglobulin G
  • Interleukin-2
  • MafK Transcription Factor
  • Nuclear Proteins
  • RNA, Messenger
  • Transcription Factor AP-1
  • Interleukin-4