Evidence map›Paper›PMID 34647200›Full record

ArticleEcotoxicology (London, England)2022

Transcriptome profiling of Arabidopsis thaliana roots in response to allelopathic effects of Conyza canadensis.

Haiyan Zhang, Susan Rutherford, Shanshan Qi, Ping Huang, Zhicong Dai, Daolin Du

Abstract read
PubMed Publisher
In one paragraph

Article in Ecotoxicology (London, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

6 citing papers in PubMed, 14 citations in OpenAlex.

  1. 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

6 authors at 1 institution in 2 countries.

Haiyan Zhang *Institute of Environment and Ecology, School of the Environment Safety Engineering, Jiangsu University, Xuefu Road 301, Zhenjiang, 212013, PR China.
Susan Rutherford *Institute of Environment and Ecology, School of the Environment Safety Engineering, Jiangsu University, Xuefu Road 301, Zhenjiang, 212013, PR China.
Shanshan QiInstitute of Agricultural Engineering, Jiangsu University, Xuefu Road 301, Zhenjiang, 212013, PR China.
Ping HuangInstitute of Environment and Ecology, School of the Environment Safety Engineering, Jiangsu University, Xuefu Road 301, Zhenjiang, 212013, PR China.
Zhicong DaiInstitute of Environment and Ecology, School of the Environment Safety Engineering, Jiangsu University, Xuefu Road 301, Zhenjiang, 212013, PR China. daizhicong@163.com.ORCID http://orcid.org/0000-0002-0748-8059
Daolin DuInstitute of Environment and Ecology, School of the Environment Safety Engineering, Jiangsu University, Xuefu Road 301, Zhenjiang, 212013, PR China. ddl@ujs.edu.cn.
Jiangsu University · CN

Funding

National Natural Science Foundation of China 32001087
6 · The paper itself

Abstract

The molecular mechanisms underlying allelopathy and their role in the interactions between invasive weeds and native species remain unclear. In this study, we aimed to explore the physiological and molecular response of plant roots of a native species to allelopathy from an invasive weed. We examined the growth and development of roots of native Arabidopsis thaliana for a 2-week period after being treated with aqueous extracts at different concentrations from invasive Conyza canadensis. Extracts with higher concentration in the Murashige and Skoog (MS) media (i.e., 4 mg of extract/mL of MS) significantly affected the root growth of A. thaliana. Roots of A. thaliana displayed weakened root tip activity and an accumulation of reactive oxygen species (ROS) in response to extracts from C. canadensis. The transcriptome analysis of A. thaliana roots exposed to phytotoxicity revealed differentially expressed genes (DEGs) involved in cell wall formation, abiotic stress, transporter genes and signal transduction. We found that genes associated with nutrient transport, such as major facilitator superfamily (MFS) and amino acid permease (AAP3) transporters as well as genes involved in stress response, including leucine-rich repeat receptor-like protein kinases (LRR-RLKs) were down-regulated. In addition, we found that many transcription factors associated with plant stress (such as APETALA2/ethylene response factors) were up-regulated while others (e.g., zinc-finger proteins) were down-regulated. Allelochemicals from C. canadensis also induced the up-regulation of detoxification (DTX) genes, ROS related genes, calcineurin B-like interacting protein kinases (CIPKs) and calmodulin. Overall, our findings provided insights into allelopathy in C. canadensis at the molecular level, and contributes to our understanding of invasion mechanisms of alien plant species. CLINICAL TRIALS REGISTRATION: This study does not contain any studies with clinical trials performed by any of the authors.

Indexed as

ArabidopsisConyzaAllelopathyGene Expression ProfilingGene Expression Regulation, PlantPlant RootsStress, PhysiologicalTranscriptomeAllelopathyGene expression profilingInvasive plantRoot growthToxicity

Identifiers

PMID34647200
OpenAlexW3207127931

What OpenQuestion holds

Textmetadata
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.