We have cloned the RAG-1 promoter region and have determined that almo
st all detectable promoter activity resides within a 208-bp fragment,
Sequence analysis of this promoter region has identified potential rec
ognition motifs for a number of lymphocyte-restricted and ubiquitous t
ranscription factors, Subsequent assays have revealed that the NF-Y tr
anscription factor interacts with a CCAAT site within the RAG-1 promot
er and appears to play an important role in the positive transcription
al regulation of this gene.