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β-Catenin is essential for patterning the maternally specified animal-vegetal axis in the sea urchin embryo

  1. William H. Klein*
  1. Department of Biochemistry and Molecular Biology, The University of Texas M. D. Anderson Cancer Center, Houston, TX 77030
  1. Communicated by William J. Lennarz, State University of New York, Stony Brook, NY (received for review March 18, 1998)

Abstract

In sea urchin embryos, the animal-vegetal axis is specified during oogenesis. After fertilization, this axis is patterned to produce five distinct territories by the 60-cell stage. Territorial specification is thought to occur by a signal transduction cascade that is initiated by the large micromeres located at the vegetal pole. The molecular mechanisms that mediate the specification events along the animal–vegetal axis in sea urchin embryos are largely unknown. Nuclear β-catenin is seen in vegetal cells of the early embryo, suggesting that this protein plays a role in specifying vegetal cell fates. Here, we test this hypothesis and show that β-catenin is necessary for vegetal plate specification and is also sufficient for endoderm formation. In addition, we show that β-catenin has pronounced effects on animal blastomeres and is critical for specification of aboral ectoderm and for ectoderm patterning, presumably via a noncell-autonomous mechanism. These results support a model in which a Wnt-like signal released by vegetal cells patterns the early embryo along the animal–vegetal axis. Our results also reveal similarities between the sea urchin animal–vegetal axis and the vertebrate dorsal–ventral axis, suggesting that these axes share a common evolutionary origin.

Footnotes

    • * To whom reprint requests should be addressed at: Department of Biochemistry and Molecular Biology, Box 117, The University of Texas M. D. Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX 77030. e-mail: wklein{at}odin.mdacc.tmc.edu.

  • ABBREVIATIONS

    GSK-3β,
    glycogen synthase kinase 3β;
    ASW,
    artificial seawater;
    RT-PCR,
    reverse transcription–PCR
    • Received March 18, 1998.
    • Accepted May 28, 1998.

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