Evidence map›Paper›PMID 32252633›Full record

ArticleBMC plant biology2020

Novel low-nitrogen stress-responsive long non-coding RNAs (lncRNA) in barley landrace B968 (Liuzhutouzidamai) at seedling stage.

Zhiwei Chen, Qi Jiang, Panpan Jiang, Wan Zhang, Jianhua Huang, Chenghong Liu, Nigel G Halford, Ruiju Lu

Open access · goldAbstract read
In one paragraph

Article in BMC plant biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.4field-weighted citation impact, top 6% 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

19 citing papers in PubMed, 28 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

8 authors at 5 institutions in 2 countries.

Zhiwei ChenBiotechnology Research Institute, Shanghai Academy of Agricultural Sciences, Shanghai, 201106, China. chenzhiwei@saas.sh.cn.
Qi JiangBiotechnology Research Institute, Shanghai Academy of Agricultural Sciences, Shanghai, 201106, China. jiangqi7281@163.com.
Panpan JiangShenzhen RealOm ics (Biotech) Co., Ltd., Shenzhen, 518081, China.
Wan ZhangSuzhou Polytechnic Institute of Agriculture, Suzhou, 215008, Jiangsu, China.
Jianhua HuangBiotechnology Research Institute, Shanghai Academy of Agricultural Sciences, Shanghai, 201106, China.
Chenghong LiuBiotechnology Research Institute, Shanghai Academy of Agricultural Sciences, Shanghai, 201106, China.
Nigel G HalfordPlant Sciences Department, Rothamsted Research, Harpenden, Hertfordshire, AL5 2JQ, UK.
Ruiju LuBiotechnology Research Institute, Shanghai Academy of Agricultural Sciences, Shanghai, 201106, China. luruiju62@163.com.
Shanghai Academy of Agricultural Sciences · CNBiotechnology Research Institute · CNLifetech Scientific (China) · CNRothamsted Research · GBSuzhou Polytechnic Institute of Agriculture · CN

Funding

Agriculture Research System of China CARS-05-01A-02Biotechnology and Biological Sciences Research Council BB/P016855/1National Natural Science Foundation of China 31601295Natural Science Foundation of Shanghai 17ZR1425300
6 · The paper itself

Abstract

backgroundReducing the dependence of crop production on chemical fertilizer with its associated costs, carbon footprint and other environmental problems is a challenge for agriculture. New solutions are required to solve this problem, and crop breeding for high nitrogen use efficiency or tolerance of low nitrogen availability has been widely considered to be a promising approach. However, the molecular mechanisms of high nitrogen use efficiency or low-nitrogen tolerance in crop plants are still to be elucidated, including the role of long non-coding RNAs (lncRNAs).

resultsIn this study, we identified 498 lncRNAs in barley (Hordeum vulgare) landrace B968 (Liuzhutouzidamai), of which 487 were novel, and characterised 56 that were responsive to low-nitrogen stress. For functional analysis of differentially-expressed lncRNAs, the gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment of co-expressed and co-located protein-coding genes were analyzed, and interactions with annotated co-expressed protein coding genes or micro RNAs (miRNAs) were further predicted. Target mimicry prediction between differentially-expressed lncRNAs and miRNAs identified 40 putative target mimics of lncRNAs and 58 target miRNAs. Six differentially-expressed lncRNAs were further validated by qPCR, and one in particular showed consistent differential expression using both techniques. Expression levels of most of the lncRNAs were found to be very low, and this may be the reason for the apparent inconsistency between RNA-seq and qPCR data.

conclusionsThe analysis of lncRNAs that are differentially-expressed under low-nitrogen stress, as well as their co-expressed or co-located protein coding genes and target mimics, could elucidate complex and hitherto uncharacterised mechanisms involved in the adaptation to low-nitrogen stress in barley and other crop plants.

Indexed as

Computational BiologyGene Expression ProfilingGene Expression Regulation, PlantGene OntologyHordeumMicroRNAsNitrogenRNA, Long NoncodingRNA, PlantRNA-SeqSeedlingsStress, PhysiologicalMicroRNAsNitrogenRNA, Long NoncodingRNA, PlantBarleyHordeum vulgareLong non-coding RNAsLow-nitrogen stressNitrogen use efficiencyRNA-seq

Identifiers

PMID32252633
PMCPMC7137197
OpenAlexW3014155869

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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.