Article

  • The EMBO Journal (1998) 17, 4414 - 4425
  • doi:10.1093/emboj/17.15.4414

The Spemann organizer-expressed zinc finger gene Xegr-1 responds to the MAP kinase/Ets-SRF signal transduction pathway

Frank Panitz1,4, Bernhard Krain2,3,4, Thomas Hollemann1, Alfred Nordheim2,3 and Tomas Pieler1

  1. Institut für Biochemie und Molekulare Zellbiologie, Universität Göttingen, Germany
  2. Institut für Molekularbiologie, Medizinische Hochschule Hannover, Germany
  3. Institut für Zellbiologie, Eberhard-Karls-Universität Tübingen, Germany
  4. F.Panitz and B.Krain contributed equally to this work

Correspondence to:

Tomas Pieler, E-mail: tpieler@gwdg.de

Received 8 May 1998; Accepted 4 June 1998; Revised 2 June 1998


The transcriptional activity of a set of genes, which are all expressed in overlapping spatial and temporal patterns within the Spemann organizer of Xenopus embryos, can be modulated by peptide growth factors. We identify Xegr-1, a zinc finger protein-encoding gene, as a novel member of this group of genes. The spatial expression characteristics of Xegr-1 during gastrulation are most similar to those of Xbra. Making use of animal cap explants, analysis of the regulatory events that govern induction of Xegr-1 gene activity reveals that, in sharp contrast to transcriptional regulation of Xbra, activation of Ets–serum response factor (SRF) transcription factor complexes is required and sufficient for Xegr-1 gene expression. This finding provides the first indication for Ets–SRF complexes bound to serum response elements to be activated during gastrulation. MAP kinase signalling cascades can induce and sustain expression of both Xegr-1 and Xbra. Ectopic Xbra can induce Xegr-1 transcription by an indirect mechanism that appears to operate via primary activation of fibroblast growth factor secretion. These findings define a cascade of events that links Xbra activity to the signal-regulated control of Xegr-1 transcription in the context of early mesoderm induction in Xenopus laevis.

  • Keywords:

    • egr-1,
    • FGF,
    • MAP kinase signalling,
    • serum response element,
    • Xenopus laevis