Regulation of Hippo signaling and planar cell polarity via distinct regions of the Fat intracellular domain
- PMID: 40377178
- PMCID: PMC12188247
- DOI: 10.1242/dev.204694
Regulation of Hippo signaling and planar cell polarity via distinct regions of the Fat intracellular domain
Abstract
The large Drosophila protocadherin Fat (Ft) is a receptor for signal transduction pathways that control growth (Hippo signaling), planar cell polarity (PCP), metabolism and the proximodistal patterning of appendages. The intracellular domain (ICD) of Ft is crucial in implementing its biological functions. Six regions of high conservation (named A-F) within the ICD have been identified, as well as distinct regions mediating Hippo pathway activity that have been functionally characterized via transgenic expression rescue assays. Here, we make targeted deletions of these highly conserved residues and the putative Hippo- and PCP-regulating domains of endogenous Ft using CRISPR/Cas9. Through transcriptomic, developmental and phenotypic analyses, we show that different regions of Ft contribute uniquely to chromatin dynamics, tissue morphogenesis, PCP and metabolic regulation. We also demonstrate that different regions of Ft regulate growth in opposite directions, with regions B and F promoting growth and region D inhibiting growth. Strikingly, conserved regions D and F are key regulators of the function of Ft in Hippo activity - exhibiting opposing effects on Hippo pathway modulation - and of the conserved regions, and D is the main regulator of PCP.
Keywords: Drosophila; Fat; Hippo; Planar cell polarity.
© 2025. Published by The Company of Biologists.
Conflict of interest statement
Competing interests The authors declare no competing or financial interests.
References
-
- Alders, M., Al-Gazali, L., Cordeiro, I., Dallapiccola, B., Garavelli, L., Tuysuz, B., Salehi, F., Haagmans, M. A., Mook, O. R., Majoie, C. B.et al. (2014). Hennekam syndrome can be caused by FAT4 mutations and be allelic to Van Maldergem syndrome. Hum. Genet. 133, 1161-1167. 10.1007/s00439-014-1456-y - DOI - PubMed
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Molecular Biology Databases
