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A single-cell Arabidopsis root atlas reveals developmental trajectories in wild-type and cell identity mutants.


ABSTRACT: In all multicellular organisms, transcriptional networks orchestrate organ development. The Arabidopsis root, with its simple structure and indeterminate growth, is an ideal model for investigating the spatiotemporal transcriptional signatures underlying developmental trajectories. To map gene expression dynamics across root cell types and developmental time, we built a comprehensive, organ-scale atlas at single-cell resolution. In addition to estimating developmental progressions in pseudotime, we employed the mathematical concept of optimal transport to infer developmental trajectories and identify their underlying regulators. To demonstrate the utility of the atlas to interpret new datasets, we profiled mutants for two key transcriptional regulators at single-cell resolution, shortroot and scarecrow. We report transcriptomic and in vivo evidence for tissue trans-differentiation underlying a mixed cell identity phenotype in scarecrow. Our results support the atlas as a rich community resource for unraveling the transcriptional programs that specify and maintain cell identity to regulate spatiotemporal organ development.

SUBMITTER: Shahan R 

PROVIDER: S-EPMC9014886 | biostudies-literature | 2022 Feb

REPOSITORIES: biostudies-literature

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A single-cell Arabidopsis root atlas reveals developmental trajectories in wild-type and cell identity mutants.

Shahan Rachel R   Hsu Che-Wei CW   Nolan Trevor M TM   Cole Benjamin J BJ   Taylor Isaiah W IW   Greenstreet Laura L   Zhang Stephen S   Afanassiev Anton A   Vlot Anna Hendrika Cornelia AHC   Schiebinger Geoffrey G   Benfey Philip N PN   Ohler Uwe U  

Developmental cell 20220207 4


In all multicellular organisms, transcriptional networks orchestrate organ development. The Arabidopsis root, with its simple structure and indeterminate growth, is an ideal model for investigating the spatiotemporal transcriptional signatures underlying developmental trajectories. To map gene expression dynamics across root cell types and developmental time, we built a comprehensive, organ-scale atlas at single-cell resolution. In addition to estimating developmental progressions in pseudotime,  ...[more]

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