Abstract

Homeodomain transcription factors of the Sine oculis (SIX) family direct multiple regulatory processes throughout the metazoans. Sine oculis (So) was first characterized in the fruit fly Drosophila melanogaster, where it is both necessary and sufficient for eye development, regulating cell survival, proliferation, and differentiation. Despite its key role in development, only a few direct targets of So have been described previously. In the current study, we aim to expand our knowledge of So-mediated transcriptional regulation in the developing Drosophila eye using ChIP-seq to map So binding regions throughout the genome. We find 7,566 So enriched regions (peaks), estimated to map to 5,952 genes. Using overlap between the So ChIP-seq peak set and genes that are differentially regulated in response to loss or gain of so, we identify putative direct targets of So. We find So binding enrichment in genes not previously known to be regulated by So, including genes that encode cell junction proteins and signaling pathway components. In addition, we analyze a subset of So-bound novel genes in the eye, and find eight genes that have previously uncharacterized eye phenotypes and may be novel direct targets of So. Our study presents a greatly expanded list of candidate So targets and serves as basis for future studies of So-mediated gene regulation in the eye.

Highlights

  • The homeodomain transcription factor Sine oculis (So) is a member of the highly conserved Retinal Determination (RD) gene network, which consists of transcriptional regulators that are both necessary and sufficient for eye development in Drosophila

  • Expression begins in the eye imaginal disc during the second instar larval stage, when the eye disc consists of proliferating retinal progenitor cells

  • Mid-third instar eye discs were chosen for the analysis as they exhibit retinal progenitors in different stages of eye development

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Summary

Introduction

The homeodomain transcription factor Sine oculis (So) is a member of the highly conserved Retinal Determination (RD) gene network, which consists of transcriptional regulators that are both necessary and sufficient for eye development in Drosophila (reviewed by [1]). The absence of So expression blocks MF initiation as well as retinal differentiation leading to massive apoptosis of the retinal progenitor cells and adult flies without eyes [3] Consistent with these observations, clonal analysis using so null mutant alleles indicates that so is required for MF initiation and progression, as well as the differentiation or survival of photoreceptor precursors posterior to the MF [5]. Despite the vital role of So in eye development, only a few direct So targets have been identified to date Most of these targets encode transcriptional regulators necessary for various stages of eye development, including the RD network genes eyeless (ey) and dachshund (dac), as well as genes that direct retinal differentiation such as atonal (ato), lozenge (lz), and prospero (pros) [6,7,8,9,10]. Regulates the expression of hedgehog (hh), which encodes a secreted ligand that drives MF progression in the eye disc [8]

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