The terminal deoxynucleotidyltransferase (TdT) gene represents an attr
active model for the analysis of gene regulation during an early phase
of lymphocyte development. In previous studies, we identified a DNA e
lement, termed D', which is essential for TdT promoter activity in imm
ature lymphocytes, and two classes of D'-binding factors, Ikaros prote
ins and Ets proteins, Here, we report a detailed mutant analysis of th
e D' element which suggests that an Ets protein, rather than an Ikaros
protein, activates TdT transcription, Since multiple Ets proteins are
expressed in developing lymphocytes and are capable of binding to the
D' element, DNA affinity chromatography was used to determine if one
of the Ets proteins might bind to the D' element with a uniquely high
affinity, thereby implicating that protein as a potential TdT activato
r, Indeed, one binding activity was greatly enriched in the high-salt
eluates from a D' affinity column, Peptide microsequencing revealed th
at the enriched protein was Elf-1. Immunoblot analyses confirmed that
in nuclear extracts, Elf-1 has a significantly higher affinity for the
D' sequence than does another Ets protein, Ets-1. Transactivation and
expression studies support the hypothesis that Elf-1 activates TdT tr
anscription in immature T and B cells, Finally, a D' mutation which se
lectively reduces Elf-1 binding, hut not the binding of other Ets prot
eins, was found to greatly reduce TdT promoter activity, Although Elf-
1 previously had been implicated in the inducible activation of genes
in mature T and B cells, our results suggest that it also plays an imp
ortant role in regulating genes during an early phase of lymphocyte de
velopment.