Abstract
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.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Amino Acid Sequence
-
Animals
-
Base Sequence
-
Binding Sites / genetics
-
Brachyury Protein
-
Calcium-Calmodulin-Dependent Protein Kinases / physiology*
-
DNA, Complementary / chemistry
-
DNA, Complementary / isolation & purification
-
DNA-Binding Proteins / antagonists & inhibitors
-
DNA-Binding Proteins / biosynthesis
-
DNA-Binding Proteins / genetics*
-
DNA-Binding Proteins / metabolism
-
DNA-Binding Proteins / physiology*
-
Early Growth Response Protein 1
-
Fetal Proteins*
-
Fibroblast Growth Factors / physiology
-
Gastrula / physiology
-
Gene Expression Regulation, Developmental*
-
Immediate-Early Proteins*
-
Molecular Sequence Data
-
Nuclear Proteins / genetics
-
Nuclear Proteins / metabolism
-
Nuclear Proteins / physiology*
-
Peptides / physiology
-
Promoter Regions, Genetic
-
Proto-Oncogene Proteins / antagonists & inhibitors
-
Proto-Oncogene Proteins / genetics
-
Proto-Oncogene Proteins / physiology*
-
Proto-Oncogene Proteins c-ets
-
Serum Response Factor
-
Signal Transduction / genetics*
-
T-Box Domain Proteins*
-
Transcription Factors / antagonists & inhibitors
-
Transcription Factors / biosynthesis
-
Transcription Factors / genetics*
-
Transcription Factors / physiology*
-
Transcription, Genetic
-
Transforming Growth Factor beta / physiology
-
Xenopus Proteins*
-
Xenopus laevis / embryology*
-
Zinc Fingers / genetics*
Substances
-
DNA, Complementary
-
DNA-Binding Proteins
-
EGR1 protein, Xenopus
-
Early Growth Response Protein 1
-
Fetal Proteins
-
Immediate-Early Proteins
-
Nuclear Proteins
-
Peptides
-
Proto-Oncogene Proteins
-
Proto-Oncogene Proteins c-ets
-
Serum Response Factor
-
T-Box Domain Proteins
-
Transcription Factors
-
Transforming Growth Factor beta
-
Xenopus Proteins
-
Fibroblast Growth Factors
-
Calcium-Calmodulin-Dependent Protein Kinases
-
Brachyury Protein