UMMS Affiliation

Molecular Genetics and Microbiology

Date

2-11-2004

Document Type

Article

Subjects

Animals; B-Lymphocytes; Green Fluorescent Proteins; Hematopoietic Stem Cells; Homeodomain Proteins; Luminescent Proteins; Lymphopoiesis; Mice; Mice, Inbred C57BL; Mice, Knockout; Mice, Transgenic; Polymerase Chain Reaction; VDJ Recombinases

Disciplines

Microbiology | Molecular Genetics

Abstract

Expression of V(D)J recombinase activity in developing lymphocytes is absolutely required for initiation of V(D)J recombination at antigen receptor loci. However, little is known about when during hematopoietic development the V(D)J recombinase is first active, nor is it known what elements activate the recombinase in multipotent hematopoietic progenitors. Using mice that express a fluorescent transgenic V(D)J recombination reporter, we show that the V(D)J recombinase is active as early as common lymphoid progenitors (CLPs) but not in the upstream progenitors that retain myeloid lineage potential. Evidence of this recombinase activity is detectable in all four progeny lineages (B, T, and NK, and DC), and rag2 levels are the highest in progenitor subsets immediately downstream of the CLP. By single cell PCR, we demonstrate that V(D)J rearrangements are detectable at IgH loci in approximately 5% of splenic natural killer cells. Finally, we show that recombinase activity in CLPs is largely controlled by the Erag enhancer. As activity of the Erag enhancer is restricted to the B cell lineage, this provides the first molecular evidence for establishment of a lineage-specific transcription program in multipotent progenitors.

Rights and Permissions

Citation: J Exp Med. 2004 Feb 16;199(4):491-502. Epub 2004 Feb 9. Link to article on publisher's site

DOI of Published Version

10.1084/jem.20031800

Related Resources

Link to Article in PubMed

Journal Title

The Journal of experimental medicine

PubMed ID

14769852

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