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Mots-C

Mitochondrial open reading frame of the 12S rRNA-c, MT-RNR1, Mitochondrial-derived peptide MOTS-c

Quick Stats
Studies 137
Trials 5
Score 2
2025 pubmed

Characterization of the Avian Mitochondrial-Derived Peptide MOTS-c and Its Potential Role as a Metabolic Regulator.

Shu. Xin X; Liu. Jiying J; Xu. Bingjie B; Wang. Hui H; Liu. Li L; Zheng. Xiaotong X; Chen. Jianfei J

Key Findings

  • Avian MOTS‑c shares high similarity with mammalian MOTS‑c but has a single‑base deletion altering downstream amino acids
  • Chicken heart shows the highest MOTS‑c expression, which decreases during fasting
  • MOTS‑c treatment in primary hepatocytes enriches ribosome, oxidative phosphorylation, and activates PI3K‑AKT and JAK‑STAT pathways

Practical Outcomes

  • While the study doesn’t give direct dosing advice, it suggests MOTS‑c could be a metabolic regulator in birds and possibly mammals. For biohackers, the data support the idea that MOTS‑c may influence energy metabolism and signaling pathways like AKT, which could be relevant when considering supplementation for metabolic health, but more human‑focused research is needed before practical protocols can be recommended.

Summary

Scientists mapped the MOTS‑c peptide in chickens and found it’s similar to the mammalian version but with a small genetic tweak that changes part of its protein sequence. The peptide is found in many chicken tissues, especially the heart, and its levels drop when the birds fast, hinting it helps regulate metabolism. In liver cells, adding MOTS‑c boosts energy‑related pathways and activates AKT signaling, which is linked to growth and metabolism.

Abstract

MOTS-c is a mitochondrial peptide that plays a crucial role in regulating energy metabolism, gene expression, and immune processes. However, current research primarily focuses on mammals like humans and mice, with no reports on avian MOTS-c. This study aimed to identify and characterize MOTS-c coding sequences across major poultry species through bioinformatics analysis and experimental validation. The alignment results showed high sequence similarity in the <i>MOTS-c</i> coding regions between avian and mammalian species. However, a single nucleotide deletion was identified in avian sequences at the position corresponding to the fourth amino acid residue of mammalian homologs, resulting in divergent downstream amino acid sequences. Despite this deletion, several residues were conserved across species. Phylogenetic analysis of mRNA sequences grouped pigeons with mammals, while protein sequence analysis revealed that poultry and mammals form separate branches, highlighting the divergence between avian and mammalian MOTS-c sequences. Tissue expression profiling demonstrated widespread distribution of chicken <i>MOTS-c</i> across multiple tissues, with the highest expression levels in the heart. Fasting significantly reduced heart <i>MOTS-c</i> expression, suggesting potential metabolic regulatory functions. Functional analysis of MOTS-c in primary hepatocytes revealed significant enrichment of the ribosome, oxidative phosphorylation, and key signaling pathways (PI3K-AKT and JAK-STAT) following 24 hours of treatment. Western blot validation confirmed MOTS-c-mediated activation of the AKT signaling pathway. This study represents the first comprehensive characterization of avian MOTS-c, providing critical insights into its evolutionary conservation and its potential functional roles in gene expression and cellular metabolism. Our findings establish a foundation for further investigation into the functions of mitochondrial-encoded peptides in avian species.

Study Information

Provider

pubmed

Year

2025

Date

2025-07-29T00:00:00.000Z

DOI

10.3390/ani15152230

References

58