Evidence map›Paper›PMID 38720464›Full record

ArticlePlant communications2024

A single-cell transcriptome atlas reveals the trajectory of early cell fate transition during callus induction in Arabidopsis.

Ruilian Yin, Ruiying Chen, Keke Xia, Xun Xu

Abstract read
In one paragraph

Article in Plant communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed.

  1. Article
  2. Article
  3. Genome-Wide Identification and Expression Analysis of theInternational journal of molecular sciences · 2026
    Article
  4. APlants (Basel, Switzerland) · 2026
    Article
  5. Cytokinin-supplemented medium drivesFrontiers in plant science · 2026
    Article
  6. Review
  7. Review
  8. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Ruilian YinCollege of Life Sciences, University of Chinese Academy of Sciences, Beijing 10049, China; BGI Research, Beijing 102601, China.
Ruiying ChenCollege of Life Sciences, University of Chinese Academy of Sciences, Beijing 10049, China; BGI Research, Beijing 102601, China.
Keke XiaBGI Research, Beijing 102601, China. Electronic address: xiakeke@genomics.cn.
Xun XuCollege of Life Sciences, University of Chinese Academy of Sciences, Beijing 10049, China; BGI Research, Beijing 102601, China; Guangdong Provincial Key Laboratory of Genome Read and Write, BGI-Shenzhen, Shenzhen 518120, Guangdong, China. Electronic address: xuxun@genomics.cn.

Funding

Non-US Government Research Support type
6 · The paper itself

Abstract

The acquisition of pluripotent callus from somatic cells plays an important role in plant development studies and crop genetic improvement. This developmental process incorporates a series of cell fate transitions and reprogramming. However, our understanding of cell heterogeneity and mechanisms of cell fate transition during callus induction remains quite limited. Here, we report a time-series single-cell transcriptome experiment on Arabidopsis root explants that were induced in callus induction medium for 0, 1, and 4 days, and the construction of a detailed single-cell transcriptional atlas of the callus induction process. We identify the cell types responsible for initiating the early callus: lateral root primordium-initiating (LRPI)-like cells and quiescent center (QC)-like cells. LRPI-like cells are derived from xylem pole pericycle cells and are similar to lateral root primordia. We delineate the developmental trajectory of the dedifferentiation of LRPI-like cells into QC-like cells. QC-like cells are undifferentiated pluripotent acquired cells that appear in the early stages of callus formation and play a critical role in later callus development and organ regeneration. We also identify the transcription factors that regulate QC-like cells and the gene expression signatures that are related to cell fate decisions. Overall, our cell-lineage transcriptome atlas for callus induction provides a distinct perspective on cell fate transitions during callus formation, significantly improving our understanding of callus formation.

Indexed as

ArabidopsisTranscriptomeCell DifferentiationGene Expression Regulation, PlantPlant RootsSingle-Cell Analysiscallus inductioncell fate transitiondevelopmental trajectorypluripotencysingle-cell RNA-seqtranscriptional regulation

Identifiers

PMID38720464
PMCPMC11369778

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.