Ribonucleotide reductase is essential, in dividing cells, for the prod
uction of deoxyribonucleotides prior to DNA synthesis in S phase. Neit
her of its two subunits (R1 and R2) are detectable in quiescent cells.
In cycling cells, RRM1 mRNA and R1 protein are present throughout the
cell cycle. A fragment of the human cDNA was used to isolate a genomi
c clone that encompasses the 5' flanking region of human RRM1. Primer
extension and PCR experiments were used to define six potential cap si
tes. The immediate upstream region does not have a TATA box and is not
GC-rich. A 1.9-kb fragment (-1670 to +208) was able to direct transcr
iption of a reporter gene in a transient expression system. Understand
ing the mechanisms regulating expression of this gene will provide ins
ight into the processes involved in cell cycling and may be of particu
lar importance in understanding the deregulated growth of transformed
cells. (C) 1994 Academic Press, Inc.