# Cell-specific Modulation of Feeding Behavior by Serotonin 2C Receptor RNA Processing > **NIH NIH R01** · VANDERBILT UNIVERSITY · 2022 · $387,560 ## Abstract The 2C-subtype of serotonin receptor (5HT2C) has been implicated in numerous human psychiatric and behavioral disorders. The best-characterized function for this receptor however, involves an anorectic response mediated by 5HT2C receptor expression in pro-opiomelanocortin (POMC)-producing neurons in the arcuate nucleus of the hypothalamus to modulate feeding behavior and energy homeostasis. Transcripts encoding the 5HT2C receptor can be modified differentially by RNA processing events that include alternative splicing and adenosine- to-inosine (A-to-I) editing. 5HT2C transcripts can undergo up to five A-to-I editing events to generate as many as 24 protein isoforms that differ in G-protein coupling efficacy and constitutive activity, while alternative splicing can produce a truncated version of the receptor (5HT2C-tr) which decreases receptor signaling by heterodimerization and sequestration of the full-length receptor within the endoplasmic reticulum. Thus, the processing of 5HT2C RNAs may represent a critical regulatory mechanism by which neurons can modulate their responsiveness to changing extracellular signals by altering the identity of functionally distinct 5HT2C isoforms expressed in specific neuronal cell types. Unfortunately, heterogeneous expression in many brain regions and within different neuronal populations has hampered efforts to understand how 5HT2C RNA processing contributes to the modulation of specific circuits or behaviors. The long-term objectives of the proposed research are to define the cellular mechanisms that regulate 5HT2C expression and signaling, as well as possible relationships between 5HT2C processing and feeding-related pathologies. Recent studies have identified alterations in both 5HT2C receptor expression and 5HT2C-mediated behaviors in mouse models and patients diagnosed with Prader-Willi Syndrome (PWS). Furthermore, mutant mice engineered solely to express the fully edited 5HT2C receptor isoform exhibit phenotypic characteristics of PWS including a failure to thrive and post-weaning hyperphagia. Thus, RNA editing and splicing have dramatic consequences on feeding behavior suggesting that improper processing of 5HT2C transcripts may represent a contributing factor to disorders of feeding and metabolism. In the current application, mutant mouse lines in which expression of the 5HT2C-tr can be induced in POMC neurons will be characterized to assess the functional importance of 5HT2C-tr modulation for 5HT2C signaling in vivo. To assess whether manipulation of 5HT2C RNA processing represents a physiological mechanism by which neuron-dependent feeding signals are modulated, three distinct model systems will be used to examine the effects of diet, exercise and pharmacologic manipulation on 5HT2C RNA processing in POMC neurons. Finally, we will test the ability of specific, edited isoforms of the 5HT2C receptor to rescue the hyperphagia, maturity-onset obesity and type II diabetes associated with the 5HT2C-null phe... ## Key facts - **NIH application ID:** 10438652 - **Project number:** 5R01DK119508-04 - **Recipient organization:** VANDERBILT UNIVERSITY - **Principal Investigator:** Ronald B. Emeson - **Activity code:** R01 (R01, R21, SBIR, etc.) - **Funding institute:** NIH - **Fiscal year:** 2022 - **Award amount:** $387,560 - **Award type:** 5 - **Project period:** 2019-08-22 → 2023-06-30 ## Primary source NIH RePORTER: https://reporter.nih.gov/project-details/10438652 ## Citation > US National Institutes of Health, RePORTER application 10438652, Cell-specific Modulation of Feeding Behavior by Serotonin 2C Receptor RNA Processing (5R01DK119508-04). Retrieved via AI Analytics 2026-05-21 from https://api.ai-analytics.org/grant/nih/10438652. Licensed CC0. --- *[NIH grants dataset](/datasets/nih-grants) · CC0 1.0*