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POSH regulates Hippo signaling through ubiquitin-mediated expanded degradation.
- Source :
-
Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2018 Feb 27; Vol. 115 (9), pp. 2150-2155. Date of Electronic Publication: 2018 Feb 12. - Publication Year :
- 2018
-
Abstract
- The Hippo signaling pathway is a master regulator of organ growth, tissue homeostasis, and tumorigenesis. The activity of the Hippo pathway is controlled by various upstream components, including Expanded (Ex), but the precise molecular mechanism of how Ex is regulated remains poorly understood. Here we identify Plenty of SH3s (POSH), an E3 ubiquitin ligase, as a key component of Hippo signaling in Drosophila POSH overexpression synergizes with loss of Kibra to induce overgrowth and up-regulation of Hippo pathway target genes. Furthermore, knockdown of POSH impedes dextran sulfate sodium-induced Yorkie-dependent intestinal stem cell renewal, suggesting a physiological role of POSH in modulating Hippo signaling. Mechanistically, POSH binds to the C-terminal of Ex and is essential for the Crumbs-induced ubiquitination and degradation of Ex. Our findings establish POSH as a crucial regulator that integrates the signal from the cell surface to negatively regulate Ex-mediated Hippo activation in Drosophila .<br />Competing Interests: The authors declare no conflict of interest.
- Subjects :
- Animals
Carrier Proteins genetics
Cytoskeletal Proteins genetics
Dextran Sulfate
Drosophila Proteins genetics
Drosophila melanogaster genetics
Gene Deletion
Genome
Intestines drug effects
Intracellular Signaling Peptides and Proteins genetics
Membrane Proteins genetics
Nerve Tissue Proteins genetics
Protein Binding
Protein Serine-Threonine Kinases genetics
Proteolysis
Signal Transduction
Stem Cells drug effects
Tumor Suppressor Proteins genetics
Tumor Suppressor Proteins metabolism
Carrier Proteins metabolism
Cytoskeletal Proteins metabolism
Drosophila Proteins metabolism
Drosophila melanogaster metabolism
Intracellular Signaling Peptides and Proteins metabolism
Membrane Proteins metabolism
Nerve Tissue Proteins metabolism
Protein Serine-Threonine Kinases metabolism
Ubiquitin metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1091-6490
- Volume :
- 115
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- Proceedings of the National Academy of Sciences of the United States of America
- Publication Type :
- Academic Journal
- Accession number :
- 29440430
- Full Text :
- https://doi.org/10.1073/pnas.1715165115