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Updated: Mar 29, 2026

Stem cell-like Xenopus Embryonic Explants to Study Early Neural Developmental Features In Vitro and In Vivo
Published on: February 2, 2016
Expression pattern of bcar3, a downstream target of Gata2, and its binding partner, bcar1, during Xenopus development
Yangsook Song Green1, Sunjong Kwon2, Jan L Christian1
1Department of Neurobiology and Anatomy, Division of Hematology and Hematologic Malignancies, University of Utah, School of Medicine, 20 North 1900 East, Salt Lake City, UT 94132, USA; Department of Internal Medicine, Division of Hematology and Hematologic Malignancies, University of Utah, School of Medicine, 20 North 1900 East, Salt Lake City, UT 94132, USA.
Abstract:
Primitive hematopoiesis generates red blood cells that deliver oxygen to the developing embryo. Mesodermal cells commit to a primitive blood cell fate during gastrulation and, in order to do so the mesoderm must receive non-cell autonomous signals transmitted from other germ layers. In Xenopus, the transcription factor Gata2 functions in ectodermal cells to generate or transmit the non-cell autonomous signals. Here we have identified Breast Cancer Antiestrogen Resistance 3 (bcar3) as a gene that is induced in ectodermal cells downstream of Gata2. Bcar3 and its binding partner Bcar1 function to transduce integrin signaling, leading to changes in cellular morphology, motility and adhesion. We show that gata2, bcar3 and bcar1 are co-expressed in ventral ectoderm from early gastrula to early tailbud stages. At later stages of development, bcar3 and bcar1 are co-expressed in the spinal cord, notochord, fin mesenchyme and pronephros but each shows additional unique sites of expression. These co-expression and unique expression patterns suggest that Bcar3 and Bcar1 may function together but also independently during Xenopus development.

