# Fat and Dachsous Signaling—Controlling Growth Requires Both Competition and Cooperation: Competitive Interactions at the Cell Cortex Restrict the Ability of an Unusual Protein Complex to Promote Tissue Growth

**Authors:** Hitoshi Matakatsu, Richard G. Fehon

PMC · DOI: 10.1002/bies.70103 · 2026-01-22

## TL;DR

This paper explains how two proteins, Dachsous and Fat, work together to control tissue growth by regulating a complex that normally promotes growth.

## Contribution

The study reveals that Dachsous and Fat can synergistically repress a growth-promoting complex, adding new insight into Hippo signaling regulation.

## Key findings

- The core complex (Dachs, Dlish, Approximated) promotes growth by repressing Warts.
- Dachsous and Fat repress the core complex by degrading it or removing it from the cell junction.
- Dachsous and Fat can function synergistically to restrict tissue growth.

## Abstract

The Hippo signaling pathway plays a key role in organ size control in normal development and tumorigenesis. While many components of this pathway are well understood, its upstream regulation remains unclear. Among the most enigmatic upstream regulators are the protocadherins Dachsous and Fat. These transmembrane proteins regulate a growth‐promoting complex composed of the atypical myosin Dachs, the adaptor protein Dlish, and the palmitoyltransferase Approximated (together termed the core complex). We propose that by default the core complex promotes growth and that Dachsous and Fat, which previously have been thought to act antagonistically, can also function synergistically to repress core complex function and therefore restrict growth. Understanding the molecular mechanisms underlying Dachsous‐Fat signaling offers insight into how multicellular organisms precisely control organ size.

Dachs, Dlish, and Approximated form a core complex at the junctional cortex that promotes growth (On) by repressing Warts. Activity of this complex is repressed (Off) both by Fat‐mediated degradation and by physical removal from the junctional cortex by Dachsous or Fat. Thus, Dachsous and Fat together repress tissue growth.

## Linked entities

- **Genes:** dachs (dachs) [NCBI Gene 34179], Dlish (Dachs ligand with SH3s) [NCBI Gene 37014], LATS1 (large tumor suppressor kinase 1) [NCBI Gene 9113], ds (dachsous) [NCBI Gene 33245], CD36 (CD36 molecule (CD36 blood group)) [NCBI Gene 948]
- **Proteins:** dachs (dachs), Dlish (Dachs ligand with SH3s), LATS1 (large tumor suppressor kinase 1), ds (dachsous), CD36 (CD36 molecule (CD36 blood group))

## Full-text entities

- **Genes:** hpo (hippo) [NCBI Gene 37247] {aka CG11228, Dmel\CG11228, Hippo, Hpo/Wts, MST, MST2}, app (approximated) [NCBI Gene 39399] {aka CG17144, CG42318, CG5620, CR32097, Dmel\CG42318, Dmel_CG17144}, CUL1 (cullin 1) [NCBI Gene 8454], Pxn (Peroxidasin) [NCBI Gene 38326] {aka CG12002, CT1239, DmPxd-a, Dmel\CG12002, Dpxn, HPX4}, Tao (Tao) [NCBI Gene 32948] {aka AAF48973, CG14217, Dmel\CG14217, MARKK, TAO-1, TAO1}, APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}, zip (zipper) [NCBI Gene 38001] {aka CG15792, DROMHC, Dm nmII, Dmel\CG15792, DmnmII, Dronm-MII}, Fbxl7 (F-box and leucine-rich repeat protein 7) [NCBI Gene 41935] {aka CG4221, Dmel\CG4221}, ds (dachsous) [NCBI Gene 33245] {aka CG17941, CT39575, Dachsous, Dmel\CG17941, EP-822, cad2}, sav (salvador) [NCBI Gene 252554] {aka CG13831, CG13832, CG33193, Dmel\CG33193, SAV1, Salvador}, Egfr (Epidermal growth factor receptor) [NCBI Gene 37455] {aka C-erb, CG10079, D-EGFR, D-Egf, DEGFR, DER}, jub (Ajuba LIM protein) [NCBI Gene 32351] {aka Ajuba, CG11063, Djub, Dmel\CG11063, dJub, djub}, fj (four-jointed) [NCBI Gene 37089] {aka CG10917, Dmel\CG10917, Fjx1}, kibra (kibra) [NCBI Gene 41783] {aka CG12600, CG33967, CG7552, DmKibra, Dmel\CG33967, Kbr}, dachs (dachs) [NCBI Gene 34179] {aka 29C3-D1, 29CD, AAF52683, CG10595, CG13087, CG31610}, wts (warts) [NCBI Gene 43651] {aka CG12072, Dlats, Dmel\CG12072, LATS, LATS1, Lats}, shg (shotgun) [NCBI Gene 37386] {aka CADH, CG3722, CT12481, Cad, CadE, Cadh}, SkpA (SKP1-related A) [NCBI Gene 31016] {aka CG16983, Dmel\CG16983, EG:115C2.4, SKP1, Skp, Skp1}, Act79B (Actin 79B) [NCBI Gene 40444] {aka 143060_f_at, ACT4, Actin, ArpF, CG7478, D}, dpp (decapentaplegic) [NCBI Gene 33432] {aka BMP, Bmp, CG9885, DPP-C, Dm-DPP, DmDPP}, CBLL2 (Cbl proto-oncogene like 2) [NCBI Gene 158506] {aka CT138, HAKAIL, ZNF645}, N (Notch) [NCBI Gene 31293] {aka 1.1, 16-178, 16-55, Ax, CG3936, CT13012}, Ubi-p63E (Ubiquitin-63E) [NCBI Gene 38456] {aka CG11624, DmUb, DmUbi-p63E, Dmel\CG11624, UB, Ub}, Vha14-1 (Vacuolar H[+] ATPase 14kD subunit 1) [NCBI Gene 36731] {aka ATP6V1F, ATPase, CG8210, Dmel\CG8210, VAF1_DROME, Vha14}, Mer (Merlin) [NCBI Gene 32979] {aka BG01543, CG14228, D-Mer, Dmel\CG14228, Dmerlin, EMR2}, crb (crumbs) [NCBI Gene 42896] {aka 0509/20, 1384/04, CG6383, CT19912, Crbs, Crumbs}, hh (hedgehog) [NCBI Gene 42737] {aka CG4637, Dmel\CG4637, Dmhh, Hg, Mir, Mrt}, dco (discs overgrown) [NCBI Gene 43673] {aka 0538/13, 0915/10, 1396/02, 1447/01, 1460/09, CG2048}, yki (yorkie) [NCBI Gene 37851] {aka CG4005, Dmel\CG4005, YAP, Yap, Yap/Taz, Yorkie}, FAT1 (FAT atypical cadherin 1) [NCBI Gene 2195] {aka CDHF7, CDHR8, FAT, ME5, hFat1}
- **Diseases:** tumor (MESH:D009369), PD patterning (MESH:C536309), tumorigenesis (MESH:D063646)
- **Chemicals:** Ft (MESH:D005223), cysteine (MESH:D003545), palmitoyl fatty acids (-), ATP (MESH:D000255)
- **Species:** Danio rerio (leopard danio, species) [taxon 7955], Homo sapiens (human, species) [taxon 9606], Drosophila melanogaster (fruit fly, species) [taxon 7227]

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12828244/full.md

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Source: https://tomesphere.com/paper/PMC12828244