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<p>Central melanocortins encoded by the <i>Pomc</i> gene control food intake and adiposity. Hypothalamic <i>Pomc</i> expression is driven by three 5′-distal enhancers known as nPE1, nPE2, and nPE3, with nPE1 carrying the strongest transcriptional capacity. Here, we investigated the functional relevance of two highly conserved canonical STAT3 motifs present in nPE1 regarding overall hypothalamic <i>Pomc</i> expression. We generated mutant mice carrying surgical co-allelic deletions of both STAT3 motifs using CRISPR-Cas9. Hypothalamic <i>Pomc</i> mRNA levels were measured by qRT-PCR in homozygous and <i>wild</i>-<i>type</i> adult littermates of both sexes, together with body weight, body length, fat mass, and food intake. A fast and refeeding test was performed with frequent measures of food intake and body weight. Using comparative genomics, we identified two highly conserved STAT3 motifs in nPE1. Homozygous female and male mice carrying simultaneous deletions of both motifs displayed 73.4 ± 0.8% and 76.5 ± 1.3% hypothalamic mRNA levels compared to same sex control littermates. Despite ~ 25% reduction in <i>Pomc</i> mRNA, body weight curves were normal across genotypes and sexes. A fast and refeeding experiment showed similar daily food intake and body weight loss and regain between homozygous and WT littermates. Our results demonstrate that the two STAT3 motifs present in the neuronal <i>Pomc</i> enhancer nPE1 are critical to reach full levels of hypothalamic <i>Pomc</i> expression.</p>

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Highly Conserved STAT3 Motifs Present in the Neuronal Pomc Enhancer nPE1 are Critical for Maximal Hypothalamic Pomc Expression

  • 期刊论文

  • 发表日期：

    2025年11月15日

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  • Clara E. Hael,
  • Malcolm J. Low,
  • Lucía F. Franchini,
  • Marcelo Rubinstein

摘要

Central melanocortins encoded by the Pomc gene control food intake and adiposity. Hypothalamic Pomc expression is driven by three 5′-distal enhancers known as nPE1, nPE2, and nPE3, with nPE1 carrying the strongest transcriptional capacity. Here, we investigated the functional relevance of two highly conserved canonical STAT3 motifs present in nPE1 regarding overall hypothalamic Pomc expression. We generated mutant mice carrying surgical co-allelic deletions of both STAT3 motifs using CRISPR-Cas9. Hypothalamic Pomc mRNA levels were measured by qRT-PCR in homozygous and wild-type adult littermates of both sexes, together with body weight, body length, fat mass, and food intake. A fast and refeeding test was performed with frequent measures of food intake and body weight. Using comparative genomics, we identified two highly conserved STAT3 motifs in nPE1. Homozygous female and male mice carrying simultaneous deletions of both motifs displayed 73.4 ± 0.8% and 76.5 ± 1.3% hypothalamic mRNA levels compared to same sex control littermates. Despite ~ 25% reduction in Pomc mRNA, body weight curves were normal across genotypes and sexes. A fast and refeeding experiment showed similar daily food intake and body weight loss and regain between homozygous and WT littermates. Our results demonstrate that the two STAT3 motifs present in the neuronal Pomc enhancer nPE1 are critical to reach full levels of hypothalamic Pomc expression.