The galectins are a family of beta-galactoside-binding proteins implic
ated in modulating cell-cell and cell-matrix interactions, Here we rep
ort the cloning and expression of a novel member of this family (galec
tin-7) that correspond to IEF (isoelectric focusing) 17 (12,700 Da; pI
, 7.6) in the human keratinocyte protein data base, and that is striki
ngly down-regulated in SV40 transformed keratinocytes (K14). The cDNA
was cloned from a lambda gt11 cDNA expression library using degenerate
d oligodeoxyribonucleotides back-translated from an IEF 17 peptide seq
uence. The protein encoded by the galectin-7 clone comigrated with IEF
17 as determined by two-dimensional (two-dimensional gel electrophore
sis) analysis of proteins expressed by transiently transfected COS-1 c
ells, and bound lactase. Alignment of the amino acid sequences with ot
her members of the family showed that the amino acids central to the b
eta-galactoside interaction are conserved. Galectin-7 was partially ex
ternalized to the medium by keratinocytes although it has no typical s
ecretion signal peptide. Immunoblotting as well as immunofluorescence
analysis of human tissues with a specific galectin-7 antibody revealed
a narrow distribution of the protein which was found mainly in strati
fied squamous epithelium. The antigen localized to basal keratinocytes
, although it was also found, albeit at lower levels, in the suprabasa
l layers where it concentrated to areas of cell to cell contact, Both,
its cellular localization as well as its striking down-regulation in
K14 keratinocytes imply a role in cell-cell and/or cell-matrix interac
tions necessary for normal growth control. The galectin-7 gene was map
ped to chromosome 19.