# Genome-wide screen for deficiencies modifying Cyclin G-induced developmental instability in Drosophila melanogaster

## TL;DR

This study explores how a specific Drosophila gene, Cyclin G, affects developmental stability and identifies genes that modify its effects on wing asymmetry.

## Contribution

A genome-wide screen in Drosophila identifies genetic deficiencies that modify developmental instability caused by Cyclin G overexpression.

## Key findings

- 495 deficiencies covering 90% of the euchromatic genome were tested for effects on wing asymmetry.
- 13 deficiencies enhance and 16 reduce developmental instability caused by Cyclin GΔP overexpression.
- Cyclin G interacts with Dpp, Wg, Hippo, and InR/TOR pathways, and Larp, to regulate organ growth and stability.

## Abstract

Despite long-lasting interest and research efforts, the genetic bases of developmental stability—the robustness to developmental noise—and its commonly used estimator, fluctuating asymmetry (FA), remain poorly understood. The Drosophila melanogaster Cyclin G gene (CycG) encodes a transcriptional cyclin that regulates growth and the cell cycle. Over-expression of a potentially more stable isoform of the protein (deletion of a PEST-rich domain, hereafter called CycGΔP) induces extreme wing size and shape FA (i.e. high developmental noise), indicating a major disruption of developmental stability. Previous attempts to identify the genetic bases of FA have been impeded by the constitutively low level of developmental noise, limiting the power to detect any effect. Here, we leverage the extreme developmental instability induced by overexpression of CycGΔP to explore the genetic bases of FA: we perform a genome-wide screen for deficiencies that enhance or reduce CycGΔP-induced wing FA. 495 deficiencies uncovering 90% of the euchromatic genome were combined with a recombinant chromosome expressing CycGΔP. We identified 13 and 16 deficiencies that respectively enhance and decrease FA. Analysis of mutants for some genes located in these deficiencies shows that Cyclin G ensures homogeneous growth of organs in synergy with the major morphogens of the wing, Dpp and Wg, as well as the Hippo and InR/TOR pathways. They also reveal that CycGΔP-induced FA involves Larp, a potential direct interactor of Cyclin G that regulates translation at the mitochondrial membrane. This opens up new research perspectives for understanding developmental stability, suggesting a significant role for mitochondrial activity.