A full-body transcription factor expression atlas with completely resolved cell identities in C. elegans

Nat Commun. 2024 Jan 9;15(1):358. doi: 10.1038/s41467-023-42677-6.

Abstract

Invariant cell lineage in C. elegans enables spatiotemporal resolution of transcriptional regulatory mechanisms controlling the fate of each cell. Here, we develop RAPCAT (Robust-point-matching- And Piecewise-affine-based Cell Annotation Tool) to automate cell identity assignment in three-dimensional image stacks of L1 larvae and profile reporter expression of 620 transcription factors in every cell. Transcription factor profile-based clustering analysis defines 80 cell types distinct from conventional phenotypic cell types and identifies three general phenotypic modalities related to these classifications. First, transcription factors are broadly downregulated in quiescent stage Hermaphrodite Specific Neurons, suggesting stage- and cell type-specific variation in transcriptome size. Second, transcription factor expression is more closely associated with morphology than other phenotypic modalities in different pre- and post-differentiation developmental stages. Finally, embryonic cell lineages can be associated with specific transcription factor expression patterns and functions that persist throughout postembryonic life. This study presents a comprehensive transcription factor atlas for investigation of intra-cell type heterogeneity.

MeSH terms

  • Animals
  • Ascomycota*
  • Caenorhabditis elegans / genetics
  • Cell Differentiation / genetics
  • Gene Expression Regulation
  • Transcription Factors* / genetics

Substances

  • Transcription Factors