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Targeted Sos1 deletion reveals its critical role in early T-cell development

  • Robert L. Kortum
  • , Connie L. Sommers
  • , Clayton P. Alexander
  • , John M. Pinski
  • , Wenmei Li
  • , Alex Grinberg
  • , Jan Lee
  • , Paul E. Love
  • , Lawrence E. Samelson*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

55 Scopus citations

Abstract

Activation of the small G protein Ras is required for thymocyte differentiation. In thymocytes, Ras is activated by the Ras guanine exchange factors (RasGEFs) Sos1, Sos2, and RasGRP1. We report the development of a floxed allele of sos1 to assess the role of Sos1 during thymocyte development. Sos1 was required for pre-T-cell receptor (pre-TCR)- but not TCR-stimulated developmental signals. Sos1 deletion led to a partial block at the DN-to-DP transition. Sos1-deficient thymocytes showed reduced pre-TCR-stimulated proliferation, differentiation, and ERK phosphorylation. In contrast, TCR-stimulated positive selection, and negative selection under strong stimulatory conditions, remained intact in Sos1-deficient mice. Comparison of RasGEF expression at different developmental stages showed that relative to Sos2 and RasGRP1, Sos1 is most abundant in DN thymocytes, but least abundant in DP thymocytes. These data reveal that Sos1 is uniquely positioned to affect signal transduction early in thymocyte development.

Original languageEnglish
Pages (from-to)12407-12412
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume108
Issue number30
DOIs
StatePublished - 26 Jul 2011

Keywords

  • β-selection
  • Conditional knockout
  • Cre
  • Lymphocyte signaling
  • Son of sevenless

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