Abstract

Nuclear receptors (NRs) comprise a family of ligand-regulated transcription factors that control diverse critical biological processes including various aspects of brain development. Eighteen NR genes exist in the Drosophila genome. To explore their roles in brain development, we knocked down individual NRs through the development of the mushroom bodies (MBs) by targeted RNAi. Besides recapitulating the known MB phenotypes for three NRs, we found that unfulfilled (unf), an ortholog of human photoreceptor specific nuclear receptor (PNR), regulates axonal morphogenesis and neuronal subtype identity. The adult MBs develop through remodeling of γ neurons plus de-novo elaboration of both α′/β′ and α/β neurons. Notably, unf is largely dispensable for the initial elaboration of γ neurons, but plays an essential role in their re-extension of axons after pruning during early metamorphosis. The subsequently derived MB neuron types also require unf for extension of axons beyond the terminus of the pruned bundle. Tracing single axons revealed misrouting rather than simple truncation. Further, silencing unf in single-cell clones elicited misguidance of axons in otherwise unperturbed MBs. Such axon guidance defects may occur as MB neurons partially lose their subtype identity, as evidenced by suppression of various MB subtype markers in unf knockdown MBs. In sum, unf governs axonal morphogenesis of multiple MB neuron types, possibly through regulating neuronal subtype identity.

Highlights

  • The brain consists of neurons that are wired in specific patterns, and establishing a complex brain involves multiple tightly regulated developmental processes

  • To study Nuclear receptors (NRs) functions in fly brain development, we generated UAS-miRNA transgenic fly lines against each of the 18 nuclear receptor (NR) genes so far identified in the fly genome

  • Ecdysone receptor (EcR) and its heterodimeric partner usp have been shown to regulate the axonal pruning of mushroom bodies (MBs) c neurons [24], and tll was recently demonstrated to promote the efficient proliferation of the MB neuroblasts and ganglion mother cells [17]

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Summary

Introduction

The brain consists of neurons that are wired in specific patterns, and establishing a complex brain involves multiple tightly regulated developmental processes. In Drosophila, it starts with birth of neuroblasts (Nbs) with specific fates that are largely acquired through spatial patterning [1]. The Nbs proliferate to produce multiple neuron types often in an invariant sequence [2,3]. Post-mitotic neurons subsequently undergo extensive morphogenesis and some neurons remodel to form the circuitry [4,5]. These basic processes are known, the detailed mechanisms that govern each step of brain development remain only partially resolved. Identifying more genes required for the various aspects of brain development is essential for elucidating further how the complex brain develops

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