The RhoA transcriptional program in pre-T cells

FEBS Lett. 2007 Sep 4;581(22):4309-17. doi: 10.1016/j.febslet.2007.07.077. Epub 2007 Aug 10.

Abstract

The GTPase RhoA is essential for the development of pre-T cells in the thymus. To investigate the mechanisms used by RhoA to control thymocyte development we have used Affymetrix gene profiling to identify RhoA regulated genes in T cell progenitors. The data show that RhoA plays a specific and essential role in pre-T cells because it is required for the expression of transcription factors of the Egr-1 and AP-1 families that have critical functions in thymocyte development. Loss of RhoA function in T cell progenitors causes a developmental block that pheno-copies the consequence of losing pre-TCR expression in Recombinase gene 2 (Rag2) null mice. Transcriptional profiling reveals both common and unique gene targets for RhoA and the pre-TCR indicating that RhoA participates in the pre-TCR induced transcriptional program but also mediates pre-TCR independent gene transcription.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ADP Ribose Transferases / metabolism
  • Animals
  • Biomarkers / metabolism
  • Botulinum Toxins / metabolism
  • Gene Expression Profiling
  • Mice
  • Mice, Inbred C57BL
  • Phosphorylation
  • Receptors, Antigen, T-Cell / metabolism
  • Ribosomal Protein S6 / metabolism
  • Stem Cells / enzymology
  • Stem Cells / metabolism*
  • T-Lymphocytes / enzymology
  • T-Lymphocytes / metabolism*
  • Thymus Gland / enzymology
  • Transcription, Genetic*
  • Up-Regulation / genetics
  • rhoA GTP-Binding Protein / metabolism*

Substances

  • Biomarkers
  • Receptors, Antigen, T-Cell
  • Ribosomal Protein S6
  • ADP Ribose Transferases
  • exoenzyme C3, Clostridium botulinum
  • Botulinum Toxins
  • rhoA GTP-Binding Protein