Evidence map›Paper›PMID 33000386›Full record

ArticlePlant molecular biology2020

DNA demethylase ROS1 prevents inheritable DREB1A/CBF3 repression by transgene-induced promoter methylation in the Arabidopsis ice1-1 mutant.

June-Sik Kim, Satoshi Kidokoro, Kazuo Shinozaki, Kazuko Yamaguchi-Shinozaki

Abstract read
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In one paragraph

Article in Plant molecular biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.6field-weighted citation impact, top 14% 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

6 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Article
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  5. Posttranslational regulation of multiple clock-related transcription factors triggers cold-inducible gene expression inProceedings of the National Academy of Sciences of the United States of America · 2021
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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 at 3 institutions in 1 country.

June-Sik KimGene Discovery Research Group, RIKEN Center for Sustainable Resource Science, Tsukuba, Ibaraki, 305-0074, Japan.ORCID http://orcid.org/0000-0002-4703-609X
Satoshi KidokoroLaboratory of Plant Molecular Physiology, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Bunkyo-ku, Tokyo, 113-8657, Japan.ORCID http://orcid.org/0000-0003-3311-4736
Kazuo ShinozakiGene Discovery Research Group, RIKEN Center for Sustainable Resource Science, Tsukuba, Ibaraki, 305-0074, Japan.ORCID http://orcid.org/0000-0002-6317-9867
Kazuko Yamaguchi-ShinozakiLaboratory of Plant Molecular Physiology, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Bunkyo-ku, Tokyo, 113-8657, Japan. akys@g.ecc.u-tokyo.ac.jp.ORCID http://orcid.org/0000-0002-0249-8258
RIKEN Center for Sustainable Resource Science · JPThe University of Tokyo · JPTokyo University of Agriculture · JP

Funding

Japan Society for the Promotion of Science 15H05960Japan Society for the Promotion of Science 17K15413Japan Society for the Promotion of Science 18H03996
6 · The paper itself

Abstract

key messageIn the ros1-defective mutant, DREB1A repression by the transgene-induced promoter methylation of ice1-1 became inheritable across generations even in the absence of the causative transgene NICE1. Transgene silencing (TGS) is a widely observed event during plant bioengineering, which is presented as a gradual decrease in ectopic gene expression across generations and occasionally coupled with endogenous gene silencing based on DNA sequence similarity. TGS is known to be established by guided DNA methylation machinery. However, the machinery underlying gene recovery from TGS has not been fully elucidated. We previously reported that in ice1-1 outcross descendants, the expressional repression and recovery of DREB1A/CBF3 were instantly achieved by a newly discovered NICE1 transgene, instead of the formerly proposed ice1-1 mutation in the ICE1 gene. The plants harboring NICE1 produced small RNAs targeting and causing the DREB1A promoter to be hypermethylated and silenced. To analyze the role of the plant-specific active DNA demethylase REPRESSOR OF SILENCING 1 (ROS1) in instant DREB1A recovery, we propagated the NICE1-segregating population upon ros1 dysfunction and evaluated the gene expression and DNA methylation levels of DREB1A through generations. Our results showed that the epigenetic DREB1A repression was substantially sustained in subsequent generations even without NICE1 and stably inherited across generations. Consistent with the gene expression results, only incomplete DNA methylation removal was detected in the same generations. These results indicate that a novel inheritable epiallele emerged by the ros1 dysfunction. Overall, our study reveals the important role of ROS1 in the inheritability of TGS-associated gene repression.

Indexed as

Gene Expression Regulation, PlantPromoter Regions, GeneticArabidopsisArabidopsis ProteinsDNA MethylationDNA, PlantInheritance PatternsNuclear ProteinsTranscription FactorsArabidopsis ProteinsDNA, PlantDREB1A protein, ArabidopsisICE1 protein, ArabidopsisNuclear ProteinsROS1 protein, ArabidopsisTranscription FactorsDNA methylationDREB1A/CBF3ice1-1NICE1ROS1Transgene silencing

Identifiers

PMID33000386
OpenAlexW3091279715

What OpenQuestion holds

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Registered trials

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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.