Regulation of prostatic genes: role of androgens and zinc in gene expression

Biochem Cell Biol. 1986 Jun;64(6):601-7. doi: 10.1139/o86-083.

Abstract

Gene expression in the rat dorsolateral prostate gland has been studied using cloned cDNA probes to the most abundant expressed mRNAs. One cDNA clone (pM-40) corresponds to two closely homologous mRNAs of about 880 nucleotides which code for two proteins of 23 and 21 kilodaltons (kDa). At least the 23-kDa protein contains a signal peptide. Another clone (pRWB) corresponds to a 1550-nucleotide mRNA which codes for a 52-kDa protein which also contains a signal peptide. The steady-state levels of these specific mRNAs increase in the dorsolateral prostate with sexual maturation. In castrated mature male rats, the M-40 mRNAs are inducible either by androgens or zinc, while the RWB mRNA is only responsive to androgens. In situ cDNA-mRNA hybridization histochemistry has been used to study the localization of the M-40 and RWB gene transcripts. Both M-40 and RWB mRNAs are most abundant in the epithelium of the lateral tip of the dorsolateral prostate. Following castration, the RWB mRNA decreases, while the M-40 mRNAs continue to be expressed in isolated areas of the epithelium. These castration-resistant cells maintain normal morphology in the absence of androgens.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Androgens / pharmacology*
  • Animals
  • Cloning, Molecular
  • Genes* / drug effects
  • Male
  • Nucleic Acid Hybridization
  • Orchiectomy
  • Organ Specificity
  • Prostate / growth & development
  • Prostate / metabolism*
  • RNA, Messenger / genetics
  • Rats
  • Sexual Maturation
  • Testosterone / pharmacology
  • Transcription, Genetic* / drug effects
  • Zinc / pharmacology*

Substances

  • Androgens
  • RNA, Messenger
  • Testosterone
  • Zinc