Human placental TEF-5 transactivates the human chorionic somatomammotropingene enhancer

Citation
Sw. Jiang et al., Human placental TEF-5 transactivates the human chorionic somatomammotropingene enhancer, MOL ENDOCR, 13(6), 1999, pp. 879-889
Citations number
32
Categorie Soggetti
Endocrinology, Nutrition & Metabolism
Journal title
MOLECULAR ENDOCRINOLOGY
ISSN journal
08888809 → ACNP
Volume
13
Issue
6
Year of publication
1999
Pages
879 - 889
Database
ISI
SICI code
0888-8809(199906)13:6<879:HPTTTH>2.0.ZU;2-T
Abstract
Human chorionic somatomammotropin (hCS) gene expression in the placenta is controlled by an enhancer (CSEn) containing SV40-related GT-IIC and SphI/Sp hII enhansons. These enhancers are controlled by members of the transcripti on enhancer factor-1 (TEF-1) family. Recently TEF-5, whose mRNA is abundant in placenta, was shown to bind cooperatively to a unique, tandemly repeate d element in CSEn2, suggesting that TEF-5 regulates CSEn activity. However, expression of TEF-5 using a cDNA lacking the 5'-untranslated region and co ntaining a modified translation initiation site was not accompanied by CSEn activation. Using nested, degenerate PCR primers corresponding to conserve d TEF domains, several novel TEF-1-related cDNAs have been cloned from a hu man placental cDNA library. The open reading frame of one 3033-bp clone was identical to TEF-5 and contained 300- and 1423-bp 5'- and 3'-untranslated regions, respectively. The in vitro generated approximately 53-kDa TEF-5 po lypeptide binds specifically to GT-IIC and SphI/SphII oligonucleotides. Ove rexpression of TEF-5 in BeWo cells using the intact 3033-bp cDNA transactiv ates the hCS and SV40 enhancers and artificial enhancers comprised of tande mly repeated GT-IIC enhansons, but not OCT enhansons. The data demonstrate that TEF-5 is a transactivator that is likely involved in the transactivati on of CSEn enhancer function. Further, the data suggest that elements withi n the untranslated regions, initiation site, or both control TEF-5 expressi on in ways that influence its transactivation function.