Evidence map›Paper›PMID 26357884›Full record

ArticleJournal of experimental botany2015

Identification, evolution, and expression partitioning of miRNAs in allopolyploid Brassica napus.

Enhui Shen, Jun Zou, Falk Hubertus Behrens, Li Chen, Chuyu Ye, Shutao Dai, Ruiyan Li, Meng Ni, Xiaoxue Jiang, Jie Qiu and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of experimental botany, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
9.3field-weighted citation impact, top 3% 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

26 citing papers in PubMed, 53 citations in OpenAlex.

  1. Article
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  10. Catalase (CAT) Gene Family in Rapeseed (International journal of molecular sciences · 2021
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  12. ComprehensiveFrontiers in genetics · 2021
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  13. Review
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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

18 authors at 6 institutions in 5 countries.

Enhui ShenInstitute of Crop Sciences & Institute of Bioinformatics, College of Agriculture and Biotechnology, Zhejiang University, Hangzhou 310058, PR China.
Jun ZouNational Key Laboratory of Crop Genetic Improvement, Huazhong Agricultural University, Wuhan 430070, PR China.
Falk Hubertus BehrensDepartment of Molecular Phytopathology and Biotechnology, Christian-Albrechts University of Kiel, Hermann Rodewald Str. 9, D-24118 Kiel, Germany.
Li ChenInstitute of Crop Sciences & Institute of Bioinformatics, College of Agriculture and Biotechnology, Zhejiang University, Hangzhou 310058, PR China.
Chuyu YeInstitute of Crop Sciences & Institute of Bioinformatics, College of Agriculture and Biotechnology, Zhejiang University, Hangzhou 310058, PR China.
Shutao DaiNational Key Laboratory of Crop Genetic Improvement, Huazhong Agricultural University, Wuhan 430070, PR China.
Ruiyan LiNational Key Laboratory of Crop Genetic Improvement, Huazhong Agricultural University, Wuhan 430070, PR China.
Meng NiNational Key Laboratory of Crop Genetic Improvement, Huazhong Agricultural University, Wuhan 430070, PR China.
Xiaoxue JiangNational Key Laboratory of Crop Genetic Improvement, Huazhong Agricultural University, Wuhan 430070, PR China.
Jie QiuInstitute of Crop Sciences & Institute of Bioinformatics, College of Agriculture and Biotechnology, Zhejiang University, Hangzhou 310058, PR China.
Yang LiuInstitute of Crop Sciences & Institute of Bioinformatics, College of Agriculture and Biotechnology, Zhejiang University, Hangzhou 310058, PR China.
Weidi WangInstitute of Crop Sciences & Institute of Bioinformatics, College of Agriculture and Biotechnology, Zhejiang University, Hangzhou 310058, PR China.
Qian-Hao ZhuCSIRO Agriculture Flagship, Canberra, ACT2601, Australia.
Boulos ChalhoubOrganization and Evolution of Plant Genomes, Unité de Recherche en Génomique Végétale, Unité Mixte de Recherche 1165 (Institut National de Recherche Agronomique, Centre National de la Recherche Scientifique, Université Evry Val d'Essonne), Evry 91057, France.
Ian BancroftCentre for Novel Agricultural Products (CNAP), Department of Biology, University of York, Wentworth Way, Heslington, York YO10 5DD, UK.
Jinling MengNational Key Laboratory of Crop Genetic Improvement, Huazhong Agricultural University, Wuhan 430070, PR China.
Daguang CaiDepartment of Molecular Phytopathology and Biotechnology, Christian-Albrechts University of Kiel, Hermann Rodewald Str. 9, D-24118 Kiel, Germany fanlj@zju.edu.cn dcai@phytomed.uni-kiel.de.
Longjiang FanInstitute of Crop Sciences & Institute of Bioinformatics, College of Agriculture and Biotechnology, Zhejiang University, Hangzhou 310058, PR China fanlj@zju.edu.cn dcai@phytomed.uni-kiel.de.
Institute of Crop Sciences · CNHuazhong Agricultural University · CNChristian-Albrechts-Universität zu Kiel · DECentre National de la Recherche Scientifique · FRCommonwealth Scientific and Industrial Research Organisation · AUUniversity of York · GB

Funding

Biotechnology and Biological Sciences Research Council BB/E017363/1
6 · The paper itself

Abstract

The recently published genome of Brassica napus offers for the first time the opportunity to gain insights into the genomic organization and the evolution of miRNAs in oilseed rape. In this study, 12 small RNA libraries from two B. napus cultivars (Tapidor and Ningyou7) and their four double-haploid lines were sequenced, employing the newly sequenced B. napus genome, together with genomes of its progenitors Brassica rapa and Brassica oleracea. A total of 645 miRNAs including 280 conserved and 365 novel miRNAs were identified. Comparative analysis revealed a high level of genomic conservation of MIRNAs (75.9%) between the subgenomes of B. napus and its two progenitors' genomes, and MIRNA lost/gain events (133) occurred in B. napus after its speciation. Furthermore, significant partitioning of miRNA expressions between the two subgenomes in B. napus was detected. The data of degradome sequencing, miRNA-mediated cleavage, and expression analyses support specific interactions between miRNAs and their targets in the modulation of diverse physiological processes in roots and leaves, as well as in biosynthesis of, for example, glucosinolates and lipids in oilseed rape. These data provide a first genome-wide view on the origin, evolution, and genomic organization of B. napus MIRNAs.

Indexed as

Brassica napusBrassica rapaChromosome MappingEvolution, MolecularGenome, PlantMicroRNAsRNA, PlantSpecies SpecificityMicroRNAsRNA, Plantallopolyploid evolutionBrassica napusexpression partitioningmicroRNA.

Identifiers

PMID26357884
PMCPMC4765792
OpenAlexW1930564483

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.