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. Author manuscript; available in PMC: 2006 Oct 2.
Published in final edited form as: Biol Reprod. 2000 Mar;62(3):670–679. doi: 10.1095/biolreprod62.3.670

FIG. 2.

FIG. 2

Nucleic acid sequence of the rat SF-1 promoter region. Sequence of the rat promoter region from −235 to +60. PCR was used to amplify the rat SF-1 promoter region using genomic DNA isolated from Sprague-Dawley rats. The sequence corresponded to that previously reported for the rat with the exception of a single-base insertion at position −41 (underlined). This change was confirmed in four independent PCR reactions. The major transcriptional start sites are indicated as bent arrows. Restriction enzyme sites used in cloning deletion mutants and potential transcription factor regulatory elements identified through the Transfac database are indicated above and below the sequence, respectively [58].