# Imp and Chinmo are required for embryonic motor neuron axon and dendrite targeting

**Authors:** Katherine H. Fisher, Sen-Lin Lai, Chris Q. Doe

PMC · DOI: 10.1242/bio.062105 · Biology Open · 2025-07-25

## TL;DR

The study shows that Imp and Chinmo are essential for motor neuron axon and dendrite targeting in fruit fly embryos.

## Contribution

The novel finding is that Imp and Chinmo are required for axon and dendrite targeting, not neuronal identity.

## Key findings

- Embryonic Imp shows a low-to-high temporal gradient, unlike larval Imp.
- Imp is required for Chinmo expression in postmitotic neurons.
- Loss of Chinmo, but not Imp, derepresses Syp expression.

## Abstract

Neural progenitors generate distinct neuronal populations over time. Drosophila larval neural progenitors, neuroblasts (NBs), generate neuronal diversity by expressing temporal gradients of transcription factors and RNA-binding proteins, including early factors Imp and Chinmo and late factors Syp, Mamo, and Broad. These factors have been well characterized in the larval central nervous system (CNS), yet nothing is known about their expression or function in the embryonic CNS. We show that embryonic Imp is expressed in a low-to-high temporal gradient, the opposite of the larval Imp gradient. Embryonic Chinmo is expressed in all post-mitotic neurons, but not in a gradient, while the late larval factors Mamo, E93, Syp, and Broad show little embryonic expression. We show that Imp is required for Chinmo expression in postmitotic neurons, and loss of Chinmo – but not Imp – derepresses Syp. Finally, we tested whether Imp and Chinmo are required for motor neuron molecular identity or morphology. Although neither is required to specify temporal or molecular neuronal identity, both are required for axon targeting to the correct body wall muscle, and downregulating dendrite outgrowth. We conclude that temporal factors are regulated differently in embryos and larvae, and that Imp and Chinmo are required for proper neuronal axon and dendrite projections.

Summary: We show that the RNA-binding protein Imp and the transcription factor Chinmo are in the same pathway that is required for proper motor neuron axon and dendrite targeting.

## Linked entities

- **Genes:** IMPA1 (inositol monophosphatase 1) [NCBI Gene 3612], chinmo (Chronologically inappropriate morphogenesis) [NCBI Gene 33343], SYP (synaptophysin) [NCBI Gene 6855], mamo (maternal gene required for meiosis) [NCBI Gene 32353], E93 (E93) [NCBI Gene 14039015], br (broad) [NCBI Gene 44505]
- **Species:** Drosophila (taxon 7215)

## Full-text entities

- **Genes:** Imp (IGF-II mRNA-binding protein) [NCBI Gene 32009] {aka CG1691, Dmel\CG1691, FGC026A04, IGF-II, IGF2BP1, IMP-1}, Syp (Syncrip) [NCBI Gene 42460] {aka AI945337, CG17838, Dmel\CG17838, anon-WO0118547.613, cg17838, l(3)03806}, chinmo (Chronologically inappropriate morphogenesis) [NCBI Gene 33343] {aka CG10871, CG17156, CG17649, CG31666, Dmel\CG31666, F}, mamo (maternal gene required for meiosis) [NCBI Gene 32353] {aka CG11071, CG11072, CG11075, CG11082, CG32606, CG32611}, Eip93F (Ecdysone-induced protein 93F) [NCBI Gene 44936] {aka CG18389, Dmel\CG18389, E93, Eip93, anon-WO02059370.58, l(3)93}
- **Species:** Drosophila melanogaster (fruit fly, species) [taxon 7227]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12352280/full.md

## References

41 references — full list in the complete paper: https://tomesphere.com/paper/PMC12352280/full.md

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Source: https://tomesphere.com/paper/PMC12352280