A molecular atlas of adult C. elegans motor neurons reveals ancient diversity delineated by conserved transcription factor codes.
Jayson J SmithSeth R TaylorJacob A BlumAaron D GitlerDavid M MillerPaschalis KratsiosPublished in: bioRxiv : the preprint server for biology (2023)
Motor neurons (MNs) constitute an ancient cell type targeted by multiple adult-onset diseases. It is therefore important to define the molecular makeup of adult MNs in animal models and extract organizing principles. Here, we generated a comprehensive molecular atlas of adult Caenorhabditis elegans MNs and a searchable database ( http://celegans.spinalcordatlas.org ). Single-cell RNA-sequencing of 13,200 cells revealed that ventral nerve cord MNs cluster into 29 molecularly distinct subclasses. All subclasses are delineated by unique expression codes of either neuropeptide or transcription factor gene families. Strikingly, we found that combinatorial codes of homeodomain transcription factor genes define adult MN diversity both in C. elegans and mice. Further, molecularly defined MN subclasses in C. elegans display distinct patterns of connectivity. Hence, our study couples the connectivity map of the C. elegans motor circuit with a molecular atlas of its constituent MNs, and uncovers organizing principles and conserved molecular codes of adult MN diversity.
Keyphrases
- transcription factor
- single cell
- rna seq
- genome wide identification
- spinal cord
- dna binding
- high throughput
- oxidative stress
- induced apoptosis
- childhood cancer
- poor prognosis
- genome wide
- type diabetes
- gene expression
- emergency department
- metabolic syndrome
- room temperature
- dna methylation
- young adults
- resting state
- signaling pathway
- white matter
- copy number
- endoplasmic reticulum stress
- drug delivery
- peripheral nerve