Table 1.
Polymorphic repeat | Sequence | Transcriptional activity, % |
---|---|---|
a | ACA GGGG TGT GGGG | 100 |
b | ACA GGGG TCT GGGG | 30.0 ± 0.4 |
Variant b | AGA GGGG TCT GGGG | 99.90 ± 0.04 |
c | ACA GGGG TCCT GGGG | 20.0 ± 0.4 |
Variant c | AGGA GGGG TCCT GGGG | 100.00 ± 0.004 |
“Restored” nucleotides are marked in bold-face. Constructs for the transfection studies were made by cloning a synthetic oligonucleotide containing four tandem copies of the corresponding polymorphic repeats upstream of the minimal prolactin-luciferase construct, Prl-luc. The transcriptional activity was determined in HeLa cells transfected in the absence and presence of a Pur-1 expression vector driven by a cytomegalovirus (CMV) promoter as described (19). Transcriptional activities of the a repeat are set arbitrarily at 100% as described in ref. 22.