Abstract

The Hippo pathway is an important regulator of organ growth and cell fate. In the R8 photoreceptor cells of the Drosophila melanogaster eye, the Hippo pathway controls the fate choice between one of two subtypes that express either the blue light-sensitive Rhodopsin 5 (Hippo inactive R8 subtype) or the green light-sensitive Rhodopsin 6 (Hippo active R8 subtype). The degree to which the mechanism of Hippo signal transduction and the proteins that mediate it are conserved in organ growth and R8 cell fate choice is currently unclear. Here, we identify Crumbs and the apical spectrin cytoskeleton as regulators of R8 cell fate. By contrast, other proteins that influence Hippo-dependent organ growth, such as the basolateral spectrin cytoskeleton and Ajuba, are dispensable for the R8 cell fate choice. Surprisingly, Crumbs promotes the Rhodopsin 5 cell fate, which is driven by Yorkie, rather than the Rhodopsin 6 cell fate, which is driven by Warts and the Hippo pathway, which contrasts with its impact on Hippo activity in organ growth. Furthermore, neither the apical spectrin cytoskeleton nor Crumbs appear to regulate the Hippo pathway through mechanisms that have been observed in growing organs. Together, these results show that only a subset of Hippo pathway proteins regulate the R8 binary cell fate decision and that aspects of Hippo signalling differ between growing organs and post-mitotic R8 cells.

Highlights

  • Binary cell fate decisions allow for the specification of a large number of cell subtypes from a small number of precursor cells

  • One such binary fate choice occurs in the R8 photoreceptor cells of the Drosophila melanogaster eye

  • To better understand Hippo signalling in R8 cells, we performed a systematic search of Hippo pathway proteins that have been implicated in organ growth but not R8 cell fate control

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Summary

Introduction

Binary cell fate decisions allow for the specification of a large number of cell subtypes from a small number of precursor cells. Binary cell fate decisions lead to a diverse range of nearly identical cells that respond to different stimuli [1,2,3]. One such binary fate choice occurs in the R8 photoreceptor cells of the Drosophila melanogaster eye. The adult D. melanogaster compound eye is composed of an array of around 800 subunits, called ommatidia, each of which contains eight photoreceptor cells (R1-R8). The outer photoreceptors, R1-6, express Rh1 and allow D. melanogaster to detect motion [7,8,9], while the inner photoreceptors, R7 and R8, express one of Rh3, Rh4, Rh5 or Rh6, and are the primary cells that mediate colour vision [10]

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