The galectin-1 gene encodes a beta-galactoside-binding protein whose o
verexpression is associated,vith neoplastic transformation and loss of
differentiation. Transient transfection assays of a series of deletio
ns constructs (pGAT) showed that the galectin-1 promoter is highly act
ive in cells both expressing and non-expressing the endogenous gene, a
nd that the basal activity is determined by sequences encompassing the
transcription start site (-50/+50). Both an upstream (-50/-26) and a
downstream position-dependent (+10/+50) cis-elements are necessary for
efficient transcriptional activity and are able to bind nuclear prote
ins.