SRD5A1 Genetic Variation and Prostate Cancer Epidemiology

Abstract

The human steroid 5-alpha reductase type I (SRD5A1) gene was sequenced in 101 men in order to identify genetic variants that might predispose carriers to prostate cancer. In these analyses, we uncovered a series of single nucleotide polymorphisms (SNPs) in the 3 -untranslated region (3 -UTR) of the SRD5A1 mRNA. However, we did not find SNPs that changed amino acid identities of the SRD5A1 protein. To further pursue the relevance of the SNPs in the 3 -UTR of this gene, we used cell culture assays to measure how they may alter RNA half-life, steady-state, and translation. Different combinations of 3 -UTR SNPs ( RNA haplotypes ) resulted in reduced SRD5A1 mRNA half-life and steady state levels in our assay system. This data is consistent with the hypothesis that SNPs in the 3 -UTRs of mRNAs may play a role in the regulation of the SRD5A1 gene. Therefore, these SNPs should be considered as candidates for having biological function that might predispose to prostate cancer.

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Document Details

Document Type
Technical Report
Publication Date
May 01, 2006
Accession Number
ADA462447

Entities

People

  • Troy Phipps

Organizations

  • University of Southern California

Tags

DTIC Thesaurus Topics

  • African Americans
  • Amino Acids
  • Cells
  • Chemical Kinetics
  • Chemistry
  • Culture Techniques
  • Diseases And Disorders
  • Genetic Variation
  • Genetics
  • Neoplasms
  • Nucleotides
  • Polymerase Chain Reaction
  • Prostate
  • Prostate Cancer
  • Rna Stability
  • Steady State
  • Translations

Fields of Study

  • Biology

Readers

  • Geochemistry
  • Gulf War Illness and Chronic Multisymptom Illness in Veterans.
  • Molecular Genetics

Technology Areas

  • Biotechnology