Free long-chain fatty acids trigger early postembryonic development in starved Caenorhabditis elegans by suppressing mTORC1

PLoS Biol. 2024 Oct 22;22(10):e3002841. doi: 10.1371/journal.pbio.3002841. eCollection 2024 Oct.

Abstract

Postembryonic development of animals has long been considered an internally predetermined program, while macronutrients were believed to be essential solely for providing biomatters and energy to support this process. However, in this study, by using a nematode Caenorhabditis elegans (abbreviated as C. elegans hereafter) model, we surprisingly discovered that dietary supplementation of palmitic acid alone, rather than other abundant essential nutrients such as glucose or amino acid mixture, was sufficient to initiate early postembryonic development even under complete macronutrient deprivation. Such a development was evidenced by changes in morphology, cellular markers in multiple tissues, behaviors, and the global transcription pattern and it occurred earlier than the well-known early L1 nutrient checkpoint. Mechanistically, palmitic acid did not function as a biomatter/energy provider, but rather as a ligand to activate the nuclear hormone receptor NHR-49/80, leading to the production of an unknown peroxisome-derived secretive hormone in the intestine. This hormonal signal was received by chemosensory neurons in the head, regulating the insulin-like neuropeptide secretion and its downstream nuclear receptor to orchestrate global development. Additionally, the nutrient-sensing hub mTORC1 played a negative role in this process. In conclusion, our data indicate that free fatty acids act as a primary nutrient signal to launch the early development in C. elegans, which suggests that specific nutrients, rather than the internal genetic program, serve as the first impetus for postembryonic development.

MeSH terms

  • Animals
  • Caenorhabditis elegans Proteins* / genetics
  • Caenorhabditis elegans Proteins* / metabolism
  • Caenorhabditis elegans* / growth & development
  • Caenorhabditis elegans* / metabolism
  • Fatty Acids / metabolism
  • Gene Expression Regulation, Developmental
  • Mechanistic Target of Rapamycin Complex 1* / metabolism
  • Neuropeptides / genetics
  • Neuropeptides / metabolism
  • Palmitic Acid / metabolism
  • Palmitic Acid / pharmacology
  • Receptors, Cytoplasmic and Nuclear / genetics
  • Receptors, Cytoplasmic and Nuclear / metabolism
  • Signal Transduction
  • Starvation / metabolism

Substances

  • Caenorhabditis elegans Proteins
  • Mechanistic Target of Rapamycin Complex 1
  • Receptors, Cytoplasmic and Nuclear
  • Palmitic Acid
  • NHR-49 protein, C elegans
  • Fatty Acids
  • Neuropeptides

Grants and funding

This work was supported by the National Natural Science Foundation of China (32170837)(HZ), the National Key R&D Program of China, 2019YFA0802804[HZ], 2021YFA08004801[HZ]), Double First-Class Initiative Fund of ShanghaiTech University (SYLDX0162022)(HZ), Science& Technology Commission of the Shanghai Municipality (16PJ1407400)(HZ), the Recruitment Program of Global Experts of China (Youth)(HZ), and ShanghaiTech Startup program (HZ). Funders did not play any role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.