Evidence map›Paper›PMID 33579187›Full record

ArticleBMC plant biology2021

Transcriptomic and genome-wide association study reveal long noncoding RNAs responding to nitrogen deficiency in maize.

Peng Ma, Xiao Zhang, Bowen Luo, Zhen Chen, Xuan He, Haiying Zhang, Binyang Li, Dan Liu, Ling Wu, Shiqiang Gao and 3 more

Open access · goldAbstract read
In one paragraph

Article in BMC plant biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
10.8field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

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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

13 citing papers in PubMed, 32 citations in OpenAlex.

  1. Exploring the CeRNA landscape in plants: advances, methods, and challenges.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2026
    Review
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  10. MicroRNA Mediated Plant Responses to Nutrient Stress.International journal of molecular sciences · 2022
    Review
  11. Article
  12. Article
  13. miRNAomic Approach to Plant Nitrogen Starvation.International journal of genomics · 2021
    Review
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

13 authors at 1 institution in 1 country.

Peng Ma *Maize Research Institute, Sichuan Agricultural University, Chengdu, 611130, Sichuan, China.
Xiao Zhang *Maize Research Institute, Sichuan Agricultural University, Chengdu, 611130, Sichuan, China.
Bowen LuoMaize Research Institute, Sichuan Agricultural University, Chengdu, 611130, Sichuan, China.
Zhen ChenMaize Research Institute, Sichuan Agricultural University, Chengdu, 611130, Sichuan, China.
Xuan HeMaize Research Institute, Sichuan Agricultural University, Chengdu, 611130, Sichuan, China.
Haiying ZhangMaize Research Institute, Sichuan Agricultural University, Chengdu, 611130, Sichuan, China.
Binyang LiMaize Research Institute, Sichuan Agricultural University, Chengdu, 611130, Sichuan, China.
Dan LiuMaize Research Institute, Sichuan Agricultural University, Chengdu, 611130, Sichuan, China.
Ling WuMaize Research Institute, Sichuan Agricultural University, Chengdu, 611130, Sichuan, China.
Shiqiang GaoMaize Research Institute, Sichuan Agricultural University, Chengdu, 611130, Sichuan, China.
Duojiang GaoMaize Research Institute, Sichuan Agricultural University, Chengdu, 611130, Sichuan, China.
Suzhi ZhangMaize Research Institute, Sichuan Agricultural University, Chengdu, 611130, Sichuan, China.
Shibin GaoMaize Research Institute, Sichuan Agricultural University, Chengdu, 611130, Sichuan, China. shibingao@163.com.ORCID http://orcid.org/0000-0001-7184-580X
Sichuan Agricultural University · CN

Funding

China Agricultural Research System CARS-02National Key Technologies Research and Development Program of China 2016YFD0100707 and 2018YFD0200707National Natural Science Foundation of China 31971955The Sichuan science and technology support project 2016NZ0103, 2016NYZ0043, and 2018HH0013
6 · The paper itself

Abstract

backgroundLong noncoding RNAs (lncRNAs) play important roles in essential biological processes. However, our understanding of lncRNAs as competing endogenous RNAs (ceRNAs) and their responses to nitrogen stress is still limited.

resultsHere, we surveyed the lncRNAs and miRNAs in maize inbred line P178 leaves and roots at the seedling stage under high-nitrogen (HN) and low-nitrogen (LN) conditions using lncRNA-Seq and small RNA-Seq. A total of 894 differentially expressed lncRNAs and 38 different miRNAs were identified. Co-expression analysis found that two lncRNAs and four lncRNA-targets could competitively combine with ZmmiR159 and ZmmiR164, respectively. To dissect the genetic regulatory by which lncRNAs might enable adaptation to limited nitrogen availability, an association mapping panel containing a high-density single-nucleotide polymorphism (SNP) array (56,110 SNPs) combined with variable LN tolerant-related phenotypes obtained from hydroponics was used for a genome-wide association study (GWAS). By combining GWAS and RNA-Seq, 170 differently expressed lncRNAs within the range of significant markers were screened. Moreover, 40 consistently LN-responsive genes including those involved in glutamine biosynthesis and nitrogen acquisition in root were identified. Transient expression assays in Nicotiana benthamiana demonstrated that LNC_002923 could inhabit ZmmiR159-guided cleavage of Zm00001d015521.

conclusionsThese lncRNAs containing trait-associated significant SNPs could consider to be related to root development and nutrient utilization. Taken together, the results of our study can provide new insights into the potential regulatory roles of lncRNAs in response to LN stress, and give valuable information for further screening of candidates as well as the improvement of maize resistance to LN stress.

Indexed as

Gene Expression Regulation, PlantGenome, PlantGenome-Wide Association StudyGlutamineMicroRNAsNicotianaNitrogenPlant ProteinsPolymorphism, Single NucleotideRNA, Long NoncodingRNA, PlantTranscriptomeZea maysGlutamineMicroRNAsNitrogenPlant ProteinsRNA, Long NoncodingRNA, PlantCo-expressionGenome-wide association studyLncRNAMaizeNitrogen use efficiencyRNA-Seq

Identifiers

PMID33579187
PMCPMC7879672
OpenAlexW3107645248

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.