A consensus Oct1 binding site is required for the activity of the Xenopus Cdx4 promoter

J.S. Reece-Hoyes, M.E. Pownall, H.V. Isaacs, I.D. Keenan

Research output: Contribution to journalArticlepeer-review

Abstract

Cdx homeodomain transcription factors have multiple roles in early vertebrate development. Furthermore, mis-regulation of Cdx expression has been demonstrated in metaplasias and cancers of the gut epithelium. Given the importance of Cdx genes in development and disease, the mechanisms underlying their expression are of considerable interest. We report an analysis of the upstream regulatory regions from the amphibian Xenopus laevis Cdx4 gene. We show that a GFP reporter containing 2.8 kb upstream of the transcription start site is expressed in the posterior of transgenic embryos. Deletion analysis of the upstream sequence reveals that a 247-bp proximal promoter fragment will drive posterior expression in transgenic embryos. We show that 63 by of upstream sequence, that includes a consensus site for POU-domain octamer-binding proteins, retains significant promoter activity. Co-expression of the octamer-binding protein Oct1 induces expression from a Cdr4 reporter and mutation of the octamer site abolishes activity of the same reporter. We show that the octamer site is highly conserved in the promoters of the human, mouse, chicken, and zebrafish Cdx4 genes and within the promoters of amphibian Cdx1 and Cdx2. These data suggest a conserved function for octamer-binding proteins in the regulation of Cdx family members. (c) 2005 Elsevier Inc. All rights reserved.

Original languageEnglish
Pages (from-to)509-523
Number of pages14
JournalDevelopmental Biology
Volume282
Issue number2
DOIs
Publication statusPublished - 15 Jun 2005

Keywords

  • Xenopus
  • Cdx4
  • POU-domain
  • Oct1
  • ANTERIOR-POSTERIOR AXIS
  • CAUDAL HOMOLOG XCAD3
  • HOMEOBOX GENE CDX1
  • HOMEODOMAIN PROTEIN
  • DOWN-REGULATION
  • HOX GENES
  • TRANSCRIPTION FACTORS
  • ANTEROPOSTERIOR AXIS
  • REGULATORY ELEMENTS
  • ECTOPIC EXPRESSION

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