Evidence map›Paper›PMID 27625667›Full record

ArticleFrontiers in plant science2016

Identification and Comparative Analysis of microRNA in Wheat (Triticum aestivum L.) Callus Derived from Mature and Immature Embryos during In vitro Culture.

Zongli Chu, Junying Chen, Haixia Xu, Zhongdong Dong, Feng Chen, Dangqun Cui

Open access · goldAbstract read
In one paragraph

Article in Frontiers in plant science, 2016. 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
5.5field-weighted citation impact, top 5% 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

16 citing papers in PubMed, 35 citations in OpenAlex.

  1. Computational Predictions and Evolutionary Analysis ofInternational journal of molecular sciences · 2026
    Article
  2. Tae-miR397 Negatively Regulates Wheat Resistance toPlants (Basel, Switzerland) · 2023
    Article
  3. Review
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  11. Epigenetic Regulation of Auxin-Induced Somatic Embryogenesis in Plants.International journal of molecular sciences · 2020
    Review
  12. Article
  13. Article
  14. Article
  15. 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

6 authors at 1 institution in 1 country.

Zongli ChuNational Key Laboratory of Wheat and Maize Science, Collaborative Innovation Center of Henan Grain Crops, Agronomy College, Henan Agricultural University Zhengzhou, China.
Junying ChenNational Key Laboratory of Wheat and Maize Science, Collaborative Innovation Center of Henan Grain Crops, Agronomy College, Henan Agricultural University Zhengzhou, China.
Haixia XuNational Key Laboratory of Wheat and Maize Science, Collaborative Innovation Center of Henan Grain Crops, Agronomy College, Henan Agricultural University Zhengzhou, China.
Zhongdong DongNational Key Laboratory of Wheat and Maize Science, Collaborative Innovation Center of Henan Grain Crops, Agronomy College, Henan Agricultural University Zhengzhou, China.
Feng ChenNational Key Laboratory of Wheat and Maize Science, Collaborative Innovation Center of Henan Grain Crops, Agronomy College, Henan Agricultural University Zhengzhou, China.
Dangqun CuiNational Key Laboratory of Wheat and Maize Science, Collaborative Innovation Center of Henan Grain Crops, Agronomy College, Henan Agricultural University Zhengzhou, China.
Henan Agricultural University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Feasible and efficient tissue culture plays an important role in plant genetic engineering. Wheat (Triticum aestivum L.) immature embryos (IMEs) are preferred for tissue culture to mature embryos (MEs) because IMEs easily generate embryogenic callus, producing large number of plants. The molecular mechanisms of regulation and the biological pathways involved in embryogenic callus formation in wheat remain unclear. Here, microRNAs (miRNAs) potentially involved in embryogenic callus formation and somatic embryogenesis were identified through deep sequencing of small RNAs (sRNAs) and analyzed with bioinformatics tools. Six sRNA libraries derived from calli of IMEs and MEs after 3, 6, or 15 d of culture (DC) were constructed and sequenced. A total of 85 known miRNAs were identified, of which 30, 33, and 18 were differentially expressed (P < 0.05) between the IME and ME libraries at 3, 6, and 15 DC, respectively. Additionally, 171 novel and 41 candidate miRNAs were also identified, of the novel miRNA, 69, 67, and 37 were differentially expressed (P < 0.05) between the two types of libraries at 3, 6, and 15 DC, respectively. The expression patterns of eight known and eight novel miRNAs were validated using quantitative real-time polymerase chain reaction. Gene ontology annotation of differentially expressed miRNA targets provided information regarding the underlying molecular functions, biological processes, and cellular components involved in embryogenic callus development. Functional miRNAs, such as miR156, miR164, miR1432, miR398, and miR397, differentially expressed in IMEs and MEs might be related to embryogenic callus formation and somatic embryogenesis. This study suggests that miRNA plays an important role in embryogenic callus formation and somatic embryogenesis in wheat, and our data provide a useful resource for further research.

Indexed as

embryogenic callusimmature embryomature embryomicroRNAwheat (Triticum aestivum L.)

Identifiers

PMID27625667
PMCPMC5003897
OpenAlexW2511896162

What OpenQuestion holds

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LicenceCC BY
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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.