Abstract

A common occurrence in metazoan development is the rise of multiple tissues/organs from a single uniform precursor field. One example is the anterior forebrain of vertebrates, which produces the eyes, hypothalamus, diencephalon, and telencephalon. Another instance is the Drosophila wing disc, which generates the adult wing blade, the hinge, and the thorax. Gene regulatory networks (GRNs) that are comprised of signaling pathways and batteries of transcription factors parcel the undifferentiated field into discrete territories. This simple model is challenged by two observations. First, many GRN members that are thought to control the fate of one organ are actually expressed throughout the entire precursor field at earlier points in development. Second, each GRN can simultaneously promote one of the possible fates choices while repressing the other alternatives. It is therefore unclear how GRNs function to allocate tissue fates if their members are uniformly expressed and competing with each other within the same populations of cells. We address this paradigm by studying fate specification in the Drosophila eye-antennal disc. The disc, which begins its development as a homogeneous precursor field, produces a number of adult structures including the compound eyes, the ocelli, the antennae, the maxillary palps, and the surrounding head epidermis. Several selector genes that control the fates of the eye and antenna, respectively, are first expressed throughout the entire eye-antennal disc. We show that during early stages, these genes are tasked with promoting the growth of the entire field. Upon segregation to distinct territories within the disc, each GRN continues to promote growth while taking on the additional roles of promoting distinct primary fates and repressing alternate fates. The timing of both expression pattern restriction and expansion of functional duties is an elemental requirement for allocating fates within a single field.

Highlights

  • In organisms as diverse as flies and humans, it is common for multiple adult tissues/organs to originate from adjacent territories within a uniform precursor field

  • A battery of transcription factors collectively called the retinal determination (RD) network controls the earliest steps in the specification of the fruit fly compound eye

  • It has been shown that gene regulatory networks (GRNs), consisting of signaling pathways and transcription factors, subdivide the precursor field and separately specify the fate of the distinct territories that are contained therein

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Summary

Introduction

In organisms as diverse as flies and humans, it is common for multiple adult tissues/organs to originate from adjacent territories within a uniform precursor field. The developing wing disc of Drosophila produces the adult wing, hinge, and thorax [3] In these instances, it has been shown that gene regulatory networks (GRNs), consisting of signaling pathways and transcription factors, subdivide the precursor field and separately specify the fate of the distinct territories that are contained therein. The GRNs that are involved in this process are thought to promote growth and specification of each tissue while acting to block tissues from adopting the wrong fate This ensures that each organ reaches the appropriate size, adopts the correct fate, is positioned properly within the body plan, and has all the requisite cell types. We have examined the role that the retinal determination (RD) network plays in the Drosophila eye-antennal disc, and our results provide a mechanistic solution to this unresolved conflict

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