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Tissue-specific promoters regulate aromatase cytochrome P450 expression

  • Evan R. Simpson
  • , Mala S. Mahendroo
  • , Gary D. Means
  • , Michael W. Kilgore
  • , C. Jo Corbin
  • , Carole R. Mendelson

Producción científica: Articlerevisión exhaustiva

110 Citas (Scopus)

Resumen

In the human, estrogen biosynthesis occurs in several tissue sites, including ovary, placenta, adipose, and brain. Recent work from our laboratory has indicated that tissue-specific expression of aromatase cytochrome P450 (P450arom), the enzyme responsible for estrogen biosynthesis, is determined, in part, by the use of tissue-specific promoters. Thus the expression of P450arom in human ovary appears to utilize a promoter proximal to the translation start-site. This promoter is not utilized in placenta but instead, the promoter used to drive aromatase expression in placenta is at least 40 kb upstream from the translational start-site. In addition, there is a minor promoter used in the expression of a small proportion of placental transcripts which is 9 kb upstream from the start of translation. Transcripts from these promoters are also expressed in other fetal tissues including placenta-related cells such as JEG-3 choriocarcinoma cells, hydatidiform moles, and other fetal tissues such as fetal liver. On the other hand, in adipose tissue expression of P450arom may be achieved by yet another, adipose-specific promoter. The various 5′-untranslated exons unique for expression driven by each of these promoters are spliced into a common intron/exon boundary upstream from the translational start-site. This means that the protein expressed in each of the various tissue-specific sites of estrogen biosynthesis is identical.

Idioma originalEnglish
Páginas (desde-hasta)321-330
Número de páginas10
PublicaciónJournal of Steroid Biochemistry and Molecular Biology
Volumen44
N.º4-6
DOI
EstadoPublished - mar 1993

Nota bibliográfica

Funding Information:
the skilled editorial assistance of Melissa Meister. This work was supported, in part, by USPHS Grants Nos AG08174 and AM31206. Gary D. Means, Mala S. Mahendroo, and Michael W. Kilgore were supported, in part, by USPHS Training Grant No. 5-T32-HD07190.

Financiación

the skilled editorial assistance of Melissa Meister. This work was supported, in part, by USPHS Grants Nos AG08174 and AM31206. Gary D. Means, Mala S. Mahendroo, and Michael W. Kilgore were supported, in part, by USPHS Training Grant No. 5-T32-HD07190.

FinanciadoresNúmero del financiador
U.S. Public Health ServiceAM31206, 5-T32-HD07190, AG08174
Eunice Kennedy Shriver National Institute of Child Health and Human DevelopmentT32HD007190

    ODS de las Naciones Unidas

    Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

    1. Good health and well being
      Good health and well being

    ASJC Scopus subject areas

    • Endocrinology, Diabetes and Metabolism
    • Biochemistry
    • Molecular Medicine
    • Molecular Biology
    • Endocrinology
    • Clinical Biochemistry
    • Cell Biology

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