Skip to content
DraconiticResearch
Search Sources API
203,234 studies31 sourcesUpdated 49 min ago
PreprintCC BYbioRxiv

An atlas of the C. elegans starvation response reveals that transcription is necessary to initiate transcriptional silencing in quiescent primordial germ cells

  1. 1Duke University

Abstract

Starvation profoundly impacts development, but how different tissues respond to starvation is unclear. We generated a cellular atlas of gene expression in fed and starved C. elegans L1 larvae. We identified 79 cell types in both conditions, and we detected [~]98% of protein-coding genes, 44% of which were differentially expressed. Starvation affected translation-related genes across the animal, and most "housekeeping" genes were downregulated. However, tissue-specific patterns of differential expression, transcription factor activity, and GO term enrichments are widespread, suggesting tissue-specific gene regulatory mechanisms and functional consequences. We inferred tissue-specific effects on transcription factor activity, identifying known and novel putative nutrient-dependent transcriptional regulators. Surprisingly, we found extensive transcription in starved primordial germ cells (PGCs), which are known to hyper-compact their chromatin and silence transcription during L1 starvation. We validated PGC transcription of aak-1/AMPK, and we showed that zygotic aak-1/AMPK is required for PGC chromatin hyper-compaction, supporting reproductive success upon recovery. This work provides a valuable resource characterizing nutritional control of transcription in an animal, and it reveals that transcription of aak-1/AMPK is necessary to silence transcription in quiescent PGCs.

Related

  1. Distinct regulation across the transcription cycle drives mitotic transcriptional silencing
    P. Gaetani, A. Tavares, T. Paixao +1
    bioRxivPreprintCC BY-NC-NDFull textCell biologybioRxiv
  2. HLH-30/TFEB is necessary for chromatin reorganization and maintenance of cell quiescence during starvation in C. elegans.
    Marta Muñoz-Barrera, Alejandro Mata-Cabana, Almudena Moreno-Rivero +6
    Nucleic acids researchPeer-reviewedCC BY-NCFull text1 citedCell biologyEurope PMC
  3. Transcriptional silencing of a conjugative Sinorhizobium megaplasmid upon transfer to different rhizobial species
    Cristina de la Cruz, Laura Cervantes, Gonzalo Torres-Tejerizo +1
    Frontiers in MicrobiologyPeer-reviewedCC BY 4.0Full textGenetics & genomicsCrossrefPMC
  4. Transcriptional activation of AaAGPase by AaGLK transcription factor determines ascorbic acid levels in kiwifruit
    Sikai Li, Ran Wang, Miaomiao Lin +5
    Horticulture researchPeer-reviewedCC BYFull textGenetics & genomicsEurope PMCEurope PMCPMC
  5. Ribosomal proteins are major substrates of starvation-induced endosomal microautophagy in Drosophila.
    P. Jaya, S. Surabhi, J. Aguilan +2
    bioRxivPreprintAll rights reservedFull textCell biologybioRxiv
BibTeX
@misc{chen2026atlas,
  title = {{An atlas of the C. elegans starvation response reveals that transcription is necessary to initiate transcriptional silencing in quiescent primordial germ cells}},
  author = {J. Chen and S. Surya and R. Chitrakar and J. R. Valley and M. F. Perez and L. R. Baugh},
  howpublished = {bioRxiv},
  year = {2026},
  month = sep,
  doi = {10.64898/2026.09.04.749554},
  url = {https://www.biorxiv.org/content/10.64898/2026.09.04.749554v1},
  note = {CC BY},
}
RIS
TY  - UNPB
TI  - An atlas of the C. elegans starvation response reveals that transcription is necessary to initiate transcriptional silencing in quiescent primordial germ cells
AU  - J. Chen
AU  - S. Surya
AU  - R. Chitrakar
AU  - J. R. Valley
AU  - M. F. Perez
AU  - L. R. Baugh
PY  - 2026
DA  - 2026/09/04
PB  - bioRxiv
DO  - 10.64898/2026.09.04.749554
UR  - https://www.biorxiv.org/content/10.64898/2026.09.04.749554v1
AB  - Starvation profoundly impacts development, but how different tissues respond to starvation is unclear. We generated a cellular atlas of gene expression in fed and starved C. elegans L1 larvae. We identified 79 cell types in both conditions, and we detected [~]98% of protein-coding genes, 44% of which were differentially expressed. Starvation affected translation-related genes across the animal, and most "housekeeping" genes were downregulated. However, tissue-specific patterns of differential expression, transcription factor activity, and GO term enrichments are widespread, suggesting tissue-specific gene regulatory mechanisms and functional consequences. We inferred tissue-specific effects on transcription factor activity, identifying known and novel putative nutrient-dependent transcriptional regulators. Surprisingly, we found extensive transcription in starved primordial germ cells (PGCs), which are known to hyper-compact their chromatin and silence transcription during L1 starvation. We validated PGC transcription of aak-1/AMPK, and we showed that zygotic aak-1/AMPK is required for PGC chromatin hyper-compaction, supporting reproductive success upon recovery. This work provides a valuable resource characterizing nutritional control of transcription in an animal, and it reveals that transcription of aak-1/AMPK is necessary to silence transcription in quiescent PGCs.
ER  -