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| Content Provider | World Health Organization (WHO)-Global Index Medicus |
|---|---|
| Author | Camp, Darius Haitian He, Billy Li, Sally Althaus, Irene W. Holtz, Alexander M. Allen, Benjamin L. Charron, Frédéric Van Meyel, Donald J. |
| Description | Author Affiliation: Camp D ( McGill Centre for Research in Neuroscience and the McGill University Health Centre Research Institute, 1650 Cedar Avenue, Montreal, Quebec, Canada H3G 1A4 Molecular Biology of Neural Development, Institut de Recherches Cliniques de Montréal (IRCM), Montreal, Quebec, Canada H2W 1R7 Division of Experi); Haitian He B ( McGill Centre for Research in Neuroscience and the McGill University Health Centre Research Institute, 1650 Cedar Avenue, Montreal, Quebec, Canada H3G 1A4.); Li S ( McGill Centre for Research in Neuroscience and the McGill University Health Centre Research Institute, 1650 Cedar Avenue, Montreal, Quebec, Canada H3G 1A4.); Althaus IW ( Department of Cell and Developmental Biology, University of Michigan, Ann Arbor, MI 48109, USA.); Holtz AM ( Department of Cell and Developmental Biology, University of Michigan, Ann Arbor, MI 48109, USA Cellular and Molecular Biology Program, University of Michigan, Ann Arbor, MI 48109, USA Medical Scientist Training Program, University of Michigan, Ann Arbor, MI 48109, USA.); Allen BL ( Department of Cell and Developmental Biology, University of Michigan, Ann Arbor, MI 48109, USA benallen@umich.edu Frederic.Charron@ircm.qc.ca don.vanmeyel@mcgill.ca.); Charron F ( Molecular Biology of Neural Development, Institut de Recherches Cliniques de Montréal (IRCM), Montreal, Quebec, Canada H2W 1R7 Division of Experimental Medicine, McGill University, Montreal, Quebec, Canada H3A 1A3 Department of Neurology and Neurosurgery, McGill University, Montreal, Quebec, Canada); van Meyel DJ ( McGill Centre for Research in Neuroscience and the McGill University Health Centre Research Institute, 1650 Cedar Avenue, Montreal, Quebec, Canada H3G 1A4 Division of Experimental Medicine, McGill University, Montreal, Quebec, Canada H3A 1A3 Department of Neurology and Neurosurgery, McGill Universit) |
| Abstract | Hedgehog (Hh) proteins are secreted molecules essential for tissue development in vertebrates and invertebrates. Hh reception via the 12-pass transmembrane protein Patched (Ptc) elicits intracellular signaling through Smoothened (Smo). Hh binding to Ptc is also proposed to sequester the ligand, limiting its spatial range of activity. In Drosophila, Interference hedgehog (Ihog) and Brother of ihog (Boi) are two conserved and redundant transmembrane proteins that are essential for Hh pathway activation. How Ihog and Boi activate signaling in response to Hh remains unknown; each can bind both Hh and Ptc and so it has been proposed that they are essential for both Hh reception and sequestration. Using genetic epistasis we established here that Ihog and Boi, and their orthologs in mice, act upstream or at the level of Ptc to allow Hh signal transduction. In the Drosophila developing wing model we found that it is through Hh pathway activation that Ihog and Boi maintain the boundary between the anterior and posterior compartments. We dissociated the contributions of Ptc from those of Ihog/Boi and, surprisingly, found that cells expressing Ptc can retain and sequester the Hh ligand without Ihog and Boi, but that Ihog and Boi cannot do so without Ptc. Together, these results reinforce the central role for Ptc in Hh binding in vivo and demonstrate that, although Ihog and Boi are dispensable for Hh sequestration, they are essential for pathway activation because they allow Hh to inhibit Ptc and thereby relieve its repression of Smo. |
| File Format | HTM / HTML |
| ISSN | 09501991 |
| e-ISSN | 14779129 |
| DOI | 10.1242/dev.103564 |
| Journal | Development |
| Issue Number | 20 |
| Volume Number | 141 |
| Language | English |
| Publisher | The Company of Biologists |
| Publisher Date | 2014-10-01 |
| Publisher Place | Great Britain (UK) |
| Access Restriction | Open |
| Subject Keyword | Discipline Developmental Discipline Biology Carrier Proteins Physiology Drosophila Proteins Membrane Glycoproteins Receptors, Cell Surface Animals Drosophila Melanogaster Embryology Epistasis, Genetic Ligands Mice Mice, Inbred C57bl Mice, Transgenic Microscopy, Fluorescence Protein Binding Recombination, Genetic Signal Transduction Spinal Cord Research Support, N.i.h., Extramural Research Support, Non-u.s. Gov't |
| Content Type | Text |
| Resource Type | Article |
| Subject | Developmental Biology Molecular Biology |
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