The diversity of the T cell receptor repertoire is generated by rearra
ngement of gene elements in immature thymocytes. To identify a thymic
signal that induces this rearrangement, a variety of agents were teste
d for their ability to induce rearrangement of the T cell receptor bet
a gene in suspensions of thymocytes from mouse embryos at day 14 of ge
station. Of 16 agents tested, only interleukin-7 (IL-7) induced V(D)J
gene rearrangement and sustained expression of the RAG-1 and RAG-2 gen
es, which are known to control rearrangement. These data implicate IL-
7, a cytokine that is abundantly expressed in embryonic thymus, in dri
ving gene rearrangement during early T cell development.