Transcriptional regulation of the Xlim-1 gene by activin is mediated by an element in intron I

  1. Martha L. Rebbert and
  2. Igor B. Dawid*
  1. Laboratory of Molecular Genetics, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892
  1. Contributed by Igor B. Dawid

Abstract

The Xlim-1 gene is activated in the late blastula stage of Xenopus embryogenesis in the mesoderm, and its RNA product becomes concentrated in the Spemann organizer at early gastrula stage. A major regulator of early expression of Xlim-1 is activin or an activin-like signal. We report experiments aiming to identify the activin response element in the Xlim-1 gene. The 5′ flanking region of the gene contains a constitutive promoter that is not activin responsive, whereas sequences in the first intron mediate repression of basal promoter activity and stimulation by activin. An intron-derived fragment of 212 nt is the smallest element that could mediate activin responsiveness. Nodal and act-Vg1, factors with signaling properties similar to activin, also stimulated Xlim-1 reporter constructs, whereas BMP-4 did not stimulate or repress the constructs. The mechanism of activin regulation of Xlim-1 and the sequence of the response element are distinct from activin response elements of other genes studied so far.

Footnotes

  • * To whom reprint requests should be addressed at: Building 6B, Room 413, National Institutes of Health, Bethesda MD 20892. e-mail: idawid{at}nih.gov.

  • Data deposition: The sequence reported in this paper has been deposited in the GenBank database (accession no. AF013242).

  • ABBREVIATIONS:
    AR,
    activin receptor;
    ARE,
    activin response element;
    BR,
    BMP receptor;
    TGF-β,
    transforming growth factor β;
    TK,
    thymidine kinase
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