Evidence map›Paper›PMID 25757472›Full record

ArticleThe Plant cell2015

The ubiquitin receptors DA1, DAR1, and DAR2 redundantly regulate endoreduplication by modulating the stability of TCP14/15 in Arabidopsis.

Yuancheng Peng, Liangliang Chen, Yaru Lu, Yingbao Wu, Jack Dumenil, Zhengge Zhu, Michael W Bevan, Yunhai Li

Open access · greenAbstract read
In one paragraph

Article in The Plant cell, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
12.4field-weighted citation impact, top 2% of its field
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

63 citing papers in PubMed, 118 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. TCP3 is a substrate of the COP1/SPA ubiquitin ligase to regulate anthocyanin accumulation and flowering time inProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  8. Review
  9. Article
  10. Review
  11. Comprehensive Analysis of theInternational journal of molecular sciences · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Genome-Wide Identification and Expression Analysis of theInternational journal of molecular sciences · 2024
    Article
  19. Review
  20. Article

3 more citing papers are in PubMed but not listed here.

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

8 authors at 4 institutions in 2 countries.

Yuancheng PengState Key Laboratory of Plant Cell and Chromosome Engineering, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China School of Life Sciences, Anhui Agricultural University, Hefei 230036, China.
Liangliang ChenState Key Laboratory of Plant Cell and Chromosome Engineering, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China.
Yaru LuState Key Laboratory of Plant Cell and Chromosome Engineering, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China College of Biological Science, Hebei Normal University, Shijiazhuang 050024, China.
Yingbao WuState Key Laboratory of Plant Cell and Chromosome Engineering, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China.
Jack DumenilDepartment of Cell and Developmental Biology, John Innes Centre, Norwich NR4 7UH, United Kingdom.
Zhengge ZhuCollege of Biological Science, Hebei Normal University, Shijiazhuang 050024, China.
Michael W BevanDepartment of Cell and Developmental Biology, John Innes Centre, Norwich NR4 7UH, United Kingdom.
Yunhai LiState Key Laboratory of Plant Cell and Chromosome Engineering, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China yhli@genetics.ac.cn.ORCID http://orcid.org/0000-0002-0025-4444
Chinese Academy of Sciences · CNJohn Innes Centre · GBAnhui Agricultural University · CNHebei Normal University · CN

Funding

Biotechnology and Biological Sciences Research Council BB/J0045881
6 · The paper itself

Abstract

Organ growth involves the coordination of cell proliferation and cell growth with differentiation. Endoreduplication is correlated with the onset of cell differentiation and with cell and organ size, but little is known about the molecular mechanisms linking cell and organ growth with endoreduplication. We have previously demonstrated that the ubiquitin receptor DA1 influences organ growth by restricting cell proliferation. Here, we show that DA1 and its close family members DAR1 and DAR2 are redundantly required for endoreduplication during leaf development. DA1, DAR1, and DAR2 physically interact with the transcription factors TCP14 and TCP15, which repress endoreduplication by directly regulating the expression of cell-cycle genes. We also show that DA1, DAR1, and DAR2 modulate the stability of TCP14 and TCP15 proteins in Arabidopsis thaliana. Genetic analyses demonstrate that DA1, DAR1, and DAR2 function in a common pathway with TCP14/15 to regulate endoreduplication. Thus, our findings define an important genetic and molecular mechanism involving the ubiquitin receptors DA1, DAR1, and DAR2 and the transcription factors TCP14 and TCP15 that links endoreduplication with cell and organ growth.

Indexed as

EndoreduplicationAmino Acid MotifsArabidopsisArabidopsis ProteinsDNA-Binding ProteinsLIM Domain ProteinsModels, BiologicalOrgan SpecificityPlant DevelopmentPlant LeavesProtein BindingProtein StabilityTranscription FactorsUbiquitinArabidopsis ProteinsDA1 protein, ArabidopsisDA1-related protein 2, ArabidopsisDNA-Binding ProteinsLIM Domain ProteinsTCP14 protein, ArabidopsisTCP15 protein, ArabidopsisTranscription FactorsUbiquitin

Identifiers

PMID25757472
PMCPMC4558651
OpenAlexW2061978392

What OpenQuestion holds

Textmetadata
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.