TY - JOUR
T1 - Hedgehog signaling patterns mesoderm in the sea urchin
AU - Walton, K D
AU - Hertzler, Philip L
N1 - Funding Information:
We thank Dr. Jenifer Croce, Dr. Cynthia Bradham, Dr. Wendy Beane and Dr. Shu-Yu Wu for helpful insights and critical comments. Dr. Sam Johnson provided imaging advice. Dr. Gary Wessel produced the myosin antibody, a small amount of which was provided by Dr. Lynne Angerer. Funding for this research was provided by NIH grants HD14483, GM61464 and PO50 GM081883 to D.R.M. and a Fellowship from the U.S. Army Medical Research and Materiel Command under W81XWH-04-1-0324 to K.D.W.
PY - 2009
Y1 - 2009
N2 - The Hedgehog (Hh) signaling pathway is essential for patterning many structures in vertebrates including the nervous system, chordamesoderm, limb and endodermal organs. In the sea urchin, a basal deuterostome, Hh signaling is shown to participate in organizing the mesoderm. At gastrulation the Hh ligand is expressed by the endoderm downstream of the Brachyury and FoxA transcription factors in the endomesoderm gene regulatory network. The co-receptors Patched (Ptc) and Smoothened (Smo) are expressed by the neighboring skeletogenic and non-skeletogenic mesoderm. Perturbations of Hh, Ptc and Smo cause embryos
to develop with skeletal defects and inappropriate non-skeletogenic mesoderm patterning, although initial specification of mesoderm occurs without detectable abnormalities. Perturbations of the pathway caused late defects in skeletogenesis and in the non-skeletogenic mesoderm, including altered numbers of pigment and blastocoelar cells, randomized left–right asymmetry of coelomic pouches, and disorganized circumesophageal
muscle causing an inability to swallow. Together the data support the requirement of Hh signaling in patterning each of the mesoderm subtypes in the sea urchin embryo.
AB - The Hedgehog (Hh) signaling pathway is essential for patterning many structures in vertebrates including the nervous system, chordamesoderm, limb and endodermal organs. In the sea urchin, a basal deuterostome, Hh signaling is shown to participate in organizing the mesoderm. At gastrulation the Hh ligand is expressed by the endoderm downstream of the Brachyury and FoxA transcription factors in the endomesoderm gene regulatory network. The co-receptors Patched (Ptc) and Smoothened (Smo) are expressed by the neighboring skeletogenic and non-skeletogenic mesoderm. Perturbations of Hh, Ptc and Smo cause embryos
to develop with skeletal defects and inappropriate non-skeletogenic mesoderm patterning, although initial specification of mesoderm occurs without detectable abnormalities. Perturbations of the pathway caused late defects in skeletogenesis and in the non-skeletogenic mesoderm, including altered numbers of pigment and blastocoelar cells, randomized left–right asymmetry of coelomic pouches, and disorganized circumesophageal
muscle causing an inability to swallow. Together the data support the requirement of Hh signaling in patterning each of the mesoderm subtypes in the sea urchin embryo.
UR - https://www.elsevier.com/developmentalbiology
M3 - Article
VL - 331
SP - 26
EP - 37
JO - Developmental Biology
JF - Developmental Biology
SN - 0012-1606
ER -