end-1 encodes an apparent GATA factor that specifies the endoderm precursor in Caenorhabditis elegans embryos (original) (raw)

  1. Jiangwen Zhu1,2,
  2. Russell J. Hill3,
  3. Paul J. Heid1,
  4. Masamitsu Fukuyama1,2,
  5. Asako Sugimoto1,5,
  6. James R. Priess3,4, and
  7. Joel H. Rothman1,2,6
  8. 1Department of Biochemistry, University of Wisconsin, Madison, Wisconsin 53706 USA; 2Department of Molecular, Cellular, and Developmental Biology and Neuroscience Research Institute, University of California, Santa Barbara, California 93106 USA; 3Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109 USA; 4Howard Hughes Medical Institute, Zoology Department, University of Washington, Seattle, Washington 98109 USA

Abstract

The endoderm in the nematode Caenorhabditis elegans is clonally derived from the E founder cell. We identified a single genomic region (the endoderm-determining region, or EDR) that is required for the production of the entire C. elegans endoderm. In embryos lacking the EDR, the E cell gives rise to ectoderm and mesoderm instead of endoderm and appears to adopt the fate of its cousin, the C founder cell. end-1, a gene from the EDR, restores endoderm production in EDR deficiency homozygotes.end-1 transcripts are first detectable specifically in the E cell, consistent with a direct role for end-1 in endoderm development. The END-1 protein is an apparent zinc finger-containing GATA transcription factor. As GATA factors have been implicated in endoderm development in other animals, our findings suggest that endoderm may be specified by molecularly conserved mechanisms in triploblastic animals. We propose that end-1, the first zygotic gene known to be involved in the specification of germ layer and founder cell identity in C. elegans, may link maternal genes that regulate the establishment of the endoderm to downstream genes responsible for endoderm differentiation.

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