Evidence map›Paper›PMID 24795531›Full record

ArticleInternational journal of biological sciences2014

Profiling of microRNAs under wound treatment in Aquilaria sinensis to identify possible microRNAs involved in agarwood formation.

Zhi-Hui Gao, Yun Yang, Zheng Zhang, Wen-Ting Zhao, Hui Meng, Yue Jin, Jun-Qing Huang, Yan-Hong Xu, Li-Zi Zhao, Juan Liu and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of biological sciences, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

8 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
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  7. Review
  8. miR394 Acts as a Negative Regulator ofFrontiers in plant science · 2018
    Article
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

11 authors at 1 institution in 1 country.

Zhi-Hui Gao1. Institute of Medicinal Plant Development, Chinese Academy of Medical Science & Peking Union Medicinal College (National Engineering Laboratory for Breeding of Endangered Medicinal Materials), Beijing 100193, China.
Yun Yang2. Hainan Branch, Institute of Medicinal Plant Development (Hainan Provincial Key Laboratory of Resources Conservation and Development of Southern Medicine), Chinese Academy of Medical Science & Peking Union Medicinal College, Wanning 571533, China.
Zheng Zhang1. Institute of Medicinal Plant Development, Chinese Academy of Medical Science & Peking Union Medicinal College (National Engineering Laboratory for Breeding of Endangered Medicinal Materials), Beijing 100193, China.
Wen-Ting Zhao1. Institute of Medicinal Plant Development, Chinese Academy of Medical Science & Peking Union Medicinal College (National Engineering Laboratory for Breeding of Endangered Medicinal Materials), Beijing 100193, China.
Hui Meng2. Hainan Branch, Institute of Medicinal Plant Development (Hainan Provincial Key Laboratory of Resources Conservation and Development of Southern Medicine), Chinese Academy of Medical Science & Peking Union Medicinal College, Wanning 571533, China.
Yue Jin1. Institute of Medicinal Plant Development, Chinese Academy of Medical Science & Peking Union Medicinal College (National Engineering Laboratory for Breeding of Endangered Medicinal Materials), Beijing 100193, China.
Jun-Qing Huang1. Institute of Medicinal Plant Development, Chinese Academy of Medical Science & Peking Union Medicinal College (National Engineering Laboratory for Breeding of Endangered Medicinal Materials), Beijing 100193, China.
Yan-Hong Xu1. Institute of Medicinal Plant Development, Chinese Academy of Medical Science & Peking Union Medicinal College (National Engineering Laboratory for Breeding of Endangered Medicinal Materials), Beijing 100193, China.
Li-Zi Zhao1. Institute of Medicinal Plant Development, Chinese Academy of Medical Science & Peking Union Medicinal College (National Engineering Laboratory for Breeding of Endangered Medicinal Materials), Beijing 100193, China.
Juan Liu1. Institute of Medicinal Plant Development, Chinese Academy of Medical Science & Peking Union Medicinal College (National Engineering Laboratory for Breeding of Endangered Medicinal Materials), Beijing 100193, China.
Jian-He Wei1. Institute of Medicinal Plant Development, Chinese Academy of Medical Science & Peking Union Medicinal College (National Engineering Laboratory for Breeding of Endangered Medicinal Materials), Beijing 100193, China ; 2. Hainan Branch, Institute of Medicinal Plant Development (Hainan Provincial Key Laboratory of Resources Conservation and Development of Southern Medicine), Chinese Academy of Medical Science & Peking Union Medicinal College, Wanning 571533, China.
Chinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Agarwood, a kind of highly valued non-timber product across Asia, is formed only when its resource trees--the endangered genus Aquilaria are wounded or infected by some microbes. To promote the efficiency of agarwood production and protect the wild resource of Aquilaria species, we urgently need to reveal the regulation mechanism of agarwood formation. MicroRNAs (miRNAs) are a group of gene expression regulators with overwhelming effects on a large spectrum of biological processes. However, their roles in agarwood formation remain unknown. This work aimed at identifying possible miRNAs involved in the wound induced agarwood formation. In this study, the high-throughput sequencing was adopted to identify miRNAs and monitor their expression under wound treatment in the stems of A. sinensis. The miR171, miR390, miR394, miR2111, and miR3954 families remained at the reduced level two days after the treatment. 131 homologous miRNAs in the 0.5 h library showed over three-fold variation of read number compared with the control library, of which 12 exhibiting strong expression alterations were further confirmed by real-time quantitative PCR. Target prediction and annotation of the miRNAs demonstrated that the binding, metabolic process, catalytic activity, and cellular process are the most common functions of the predicted targets of these newly identified miRNAs in A.sinensis. The cleaveage sites of three newly predicted targets were verified by 5'RACE.

Indexed as

Base SequenceGene Expression ProfilingGene Expression Regulation, PlantHigh-Throughput Nucleotide SequencingMicroRNAsMolecular Sequence DataReal-Time Polymerase Chain ReactionResins, PlantReverse Transcriptase Polymerase Chain ReactionThymelaeaceaeWoodWound HealingMicroRNAsResins, PlantAgarwoodAquilaria sinensismicroRNAsmall RNAwound

Identifiers

PMID24795531
PMCPMC4007363
OpenAlexW2114175275

What OpenQuestion holds

Textmetadata
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.