Evidence map›Paper›PMID 26342708›Full record

ArticlePlanta2016

High-throughput sequencing and degradome analysis reveal neutral evolution of Cercis gigantea microRNAs and their targets.

Wenna Guo, Ying Zhang, Qiang Wang, Yueping Zhan, Guanghui Zhu, Qi Yu, Liucun Zhu

Open access · hybridAbstract readComparative Study
In one paragraph

Article in Planta, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

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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

7 authors at 3 institutions in 1 country.

Wenna GuoSchool of Life Sciences, Shanghai University, Shanghai, 200444, People's Republic of China. gwn0807@shu.edu.cn.
Ying ZhangYangzhou Breeding Biological Agriculture Technology Co. Ltd, Yangzhou, 225200, People's Republic of China. zhyingfly@163.com.
Qiang WangState Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing, 210093, People's Republic of China. Wangq@nju.edu.cn.
Yueping ZhanSchool of Life Sciences, Shanghai University, Shanghai, 200444, People's Republic of China. zhanyp@shu.edu.cn.
Guanghui ZhuSchool of Life Sciences, Shanghai University, Shanghai, 200444, People's Republic of China. moonshadowzhu@gmail.com.
Qi YuDepartment of Radiation Oncology, Fudan University Shanghai Cancer Center, Shanghai, People's Republic of China. yuphar@126.com.
Liucun ZhuSchool of Life Sciences, Shanghai University, Shanghai, 200444, People's Republic of China. zhuliucun1983@163.com.
Shanghai University · CNFudan University Shanghai Cancer Center · CNNanjing University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MAIN

conclusionHigh-throughput sequencing and degradome analysis for Cercis gigantea identified 194 known miRNAs and 23 novel miRNAs with 61 targets. The comparison results of highly conserved miRNAs and non-conserved miRNAs implied that C. gigantea miRNAs were subjected to the neutral evolution. MicroRNAs play a key role in post-transcriptionally regulating gene expression during plant growth, development and other various biological processes. Although numerous miRNAs have been identified and documented, to date, there are no reports on Cercis gigantea (C. gigantea) miRNAs. In this study, C. gigantea miRNAs and their target genes were investigated by extracting RNA from young roots, tender stems, young leaves, and flower buds of C. gigantea to establish a small RNA and a degradome library to further sequence. This study identified 194 known miRNAs belonging to 52 miRNA families and 23 novel miRNAs. Among these, 158 miRNAs from 27 miRNA families were highly conserved and existed in a plurality of plants. In addition, 60 different targets for 30 known families and one target for novel miRNA were identified by high-throughput sequencing and degradome analysis in C. gigantea. The comparison results revealed that highly conserved miRNAs have higher expression levels, more family members and more targets than non-conserved miRNAs, indicating that C. gigantea miRNAs were subjected to the neutral evolution. Meanwhile, these conserved miRNAs were also found to be involved in auxin signal transduction, regulation of transcription, and other developmental processes, which will help further understanding regulatory mechanisms of C. gigantea miRNAs.

Indexed as

EndoribonucleasesGenetic DriftMultienzyme ComplexesPolyribonucleotide NucleotidyltransferaseRNA HelicasesRNA Processing, Post-TranscriptionalBase SequenceFabaceaeFlowersGene Expression Regulation, PlantGene LibraryHigh-Throughput Nucleotide SequencingMicroRNAsPlant LeavesPlant RootsPlant StemsdegradosomeEndoribonucleasesMicroRNAsMultienzyme ComplexesPolyribonucleotide NucleotidyltransferaseRNA HelicasesRNA, PlantDegradome analysisHigh-throughput sequencingLegumemiRNANeutral evolution

Identifiers

PMID26342708
PMCPMC4698290
OpenAlexW1826249740

What OpenQuestion holds

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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.