Regulation of miR-219 and its target RalGPS is essential for synaptic plasticity at the Drosophila neuromuscular junction
- 1Department of Cell Biology, Harvard Medical School, Boston, MA 02115
Abstract
RNA regulatory mechanisms mediate adaptive responses relying on rapid changes in gene expression. By examining microRNA (miRNA)-mediated control of structural synaptic plasticity, we find miR-219 and five other conserved miRNAs regulate activity-induced morphogenesis at Drosophila glutamatergic synapses. Among miRNA targets downregulated by acute stimulation, the Ral activating factor RalGPS is necessary for presynaptic morphogenesis and is sufficient to block plasticity. We find that RalGPS must be held within a narrow range of expression for structural remodeling to occur. Loss or excess of RalGPS both abolish activity-induced synapse growth. Without altering levels of mature miR-219, stimulation elevates miR-219 loading in Argonaute (Ago1)-containing complexes that mediate miRNA gene silencing. We also find that elevated Protein Kinase A activity suppresses miR-219 association with Ago1 and blocks activity-induced synaptic growth, suggesting that miRNA loading and unloading in neurons are both controlled by activity-dependent regulation of Ago1.
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BibTeX
@article{aavula2026regulation,
title = {{Regulation of miR-219 and its target RalGPS is essential for synaptic plasticity at the Drosophila neuromuscular junction}},
author = {Kumar Aavula and Hansine Heggeness and Takakazu Yokokura and Spyros Artavanis-Tsakonas and David Van Vactor},
journal = {Proceedings of the National Academy of Sciences of the United States of America},
year = {2026},
month = oct,
doi = {10.1073/pnas.2622609123},
url = {https://doi.org/10.1073/pnas.2622609123},
note = {CC BY-NC-ND 4.0},
}
RIS
TY - JOUR
TI - Regulation of miR-219 and its target RalGPS is essential for synaptic plasticity at the Drosophila neuromuscular junction
AU - Kumar Aavula
AU - Hansine Heggeness
AU - Takakazu Yokokura
AU - Spyros Artavanis-Tsakonas
AU - David Van Vactor
PY - 2026
DA - 2026/10/27
JO - Proceedings of the National Academy of Sciences of the United States of America
DO - 10.1073/pnas.2622609123
UR - https://doi.org/10.1073/pnas.2622609123
AB - RNA regulatory mechanisms mediate adaptive responses relying on rapid changes in gene expression. By examining microRNA (miRNA)-mediated control of structural synaptic plasticity, we find miR-219 and five other conserved miRNAs regulate activity-induced morphogenesis at Drosophila glutamatergic synapses. Among miRNA targets downregulated by acute stimulation, the Ral activating factor RalGPS is necessary for presynaptic morphogenesis and is sufficient to block plasticity. We find that RalGPS must be held within a narrow range of expression for structural remodeling to occur. Loss or excess of RalGPS both abolish activity-induced synapse growth. Without altering levels of mature miR-219, stimulation elevates miR-219 loading in Argonaute (Ago1)-containing complexes that mediate miRNA gene silencing. We also find that elevated Protein Kinase A activity suppresses miR-219 association with Ago1 and blocks activity-induced synaptic growth, suggesting that miRNA loading and unloading in neurons are both controlled by activity-dependent regulation of Ago1.
SN - 0027-8424
SN - 1091-6490
ER -