<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Xia Y</submitter><funding>NIGMS NIH HHS</funding><pubmed_abstract>The circadian clock enables organisms to optimize their metabolism, physiology, and behavior with the time-of-day. However, circadian rhythms benefit organisms only if they are properly synchronized with the day/night cycle; circadian misalignment can have detrimental effects on animals' wellbeing and survival. We previously showed that in &lt;i>Drosophila&lt;/i>, loss of the microRNA &lt;i>miR-124&lt;/i> advances the phase of circadian evening locomotor activity by several hours under constant darkness conditions. Interestingly, we now report that loss of &lt;i>miR-124&lt;/i> also delays morning activity under a light/dark cycle with a short photoperiod. We recapitulated these opposite phase phenotypes by eliminating &lt;i>miR-124&lt;/i> during larval development, but not when this microRNA is lost during pupation to adulthood. The loss of &lt;i>miR-124&lt;/i> results in significant miswiring within the circadian neural network and severely alters neural activity rhythms in the ventral Lateral Neurons (s-LNvs) and the posterior Dorsal Neurons 1 (DN1ps), which control the timing of morning and evening activity. Silencing the s-LNvs in &lt;i>miR-124&lt;/i> mutant flies restores the phase of evening activity, while activating the DN1ps rescues the phases of both morning and evening activities. Our findings thus reveal the pivotal role of &lt;i>miR-124&lt;/i> in sculpting the &lt;i>Drosophila&lt;/i> circadian neural network during development and its long-lasting impact on circuit activity and adult circadian behavior.</pubmed_abstract><journal>Journal of biological rhythms</journal><pagination>7487304251361579</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12404682</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>&amp;lt;i&amp;gt;miR-124&amp;lt;/i&amp;gt; acts During &amp;lt;i&amp;gt;Drosophila&amp;lt;/i&amp;gt; Development to Determine the Phase of Adult Circadian Behavior.</pubmed_title><pmcid>PMC12404682</pmcid><funding_grant_id>R35 GM145253</funding_grant_id><pubmed_authors>Xia Y</pubmed_authors><pubmed_authors>Emery P</pubmed_authors><pubmed_authors>Chen C</pubmed_authors></additional><is_claimable>false</is_claimable><name>&amp;lt;i&amp;gt;miR-124&amp;lt;/i&amp;gt; acts During &amp;lt;i&amp;gt;Drosophila&amp;lt;/i&amp;gt; Development to Determine the Phase of Adult Circadian Behavior.</name><description>The circadian clock enables organisms to optimize their metabolism, physiology, and behavior with the time-of-day. However, circadian rhythms benefit organisms only if they are properly synchronized with the day/night cycle; circadian misalignment can have detrimental effects on animals' wellbeing and survival. We previously showed that in &lt;i>Drosophila&lt;/i>, loss of the microRNA &lt;i>miR-124&lt;/i> advances the phase of circadian evening locomotor activity by several hours under constant darkness conditions. Interestingly, we now report that loss of &lt;i>miR-124&lt;/i> also delays morning activity under a light/dark cycle with a short photoperiod. We recapitulated these opposite phase phenotypes by eliminating &lt;i>miR-124&lt;/i> during larval development, but not when this microRNA is lost during pupation to adulthood. The loss of &lt;i>miR-124&lt;/i> results in significant miswiring within the circadian neural network and severely alters neural activity rhythms in the ventral Lateral Neurons (s-LNvs) and the posterior Dorsal Neurons 1 (DN1ps), which control the timing of morning and evening activity. Silencing the s-LNvs in &lt;i>miR-124&lt;/i> mutant flies restores the phase of evening activity, while activating the DN1ps rescues the phases of both morning and evening activities. Our findings thus reveal the pivotal role of &lt;i>miR-124&lt;/i> in sculpting the &lt;i>Drosophila&lt;/i> circadian neural network during development and its long-lasting impact on circuit activity and adult circadian behavior.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Aug</publication><modification>2026-05-29T16:59:48.876Z</modification><creation>2026-04-08T05:26:55.503Z</creation></dates><accession>S-EPMC12404682</accession><cross_references><pubmed>40879142</pubmed><doi>10.1177/07487304251361579</doi></cross_references></HashMap>