Matches in SemOpenAlex for { <https://semopenalex.org/work/W2110195338> ?p ?o ?g. }
- W2110195338 abstract "Regeneration of damaged tissues typically requires a population of active stem cells. How damaged tissue is regenerated in quiescent tissues lacking a stem cell population is less well understood. We used a genetic screen in the developing Drosophila melanogaster eye to investigate the mechanisms that trigger quiescent cells to re-enter the cell cycle and proliferate in response to tissue damage. We discovered that Hippo signaling regulates compensatory proliferation after extensive cell death in the developing eye. Scalloped and Yorkie, transcriptional effectors of the Hippo pathway, drive Cyclin E expression to induce cell cycle re-entry in cells that normally remain quiescent in the absence of damage. Ajuba, an upstream regulator of Hippo signaling that functions as a sensor of epithelial integrity, is also required for cell cycle re-entry. Thus, in addition to its well-established role in modulating proliferation during periods of tissue growth, Hippo signaling maintains homeostasis by regulating quiescent cell populations affected by tissue damage." @default.
- W2110195338 created "2016-06-24" @default.
- W2110195338 creator A5069472220 @default.
- W2110195338 creator A5089762109 @default.
- W2110195338 date "2015-01-01" @default.
- W2110195338 modified "2023-10-12" @default.
- W2110195338 title "Scalloped and Yorkie are required for cell cycle re-entry of quiescent cells after tissue damage" @default.
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- W2110195338 doi "https://doi.org/10.1242/dev.119339" @default.
- W2110195338 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4550963" @default.
- W2110195338 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/26160905" @default.
- W2110195338 hasPublicationYear "2015" @default.
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