Evidence map›Paper›PMID 35486290›Full record

ArticlePlant molecular biology2022

Construction of two regulatory networks related to salt stress and lignocellulosic synthesis under salt stress based on a Populus davidiana × P. bolleana transcriptome analysis.

Xiaojin Lei, Zhongyuan Liu, Qingjun Xie, Jiaru Fang, Chunyao Wang, Jinghang Li, Chao Wang, Caiqiu Gao

Abstract read
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In one paragraph

Article in Plant molecular biology, 2022. 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
1.6field-weighted citation impact, top 17% 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

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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, 18 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 1 institution in 1 country.

Xiaojin Lei *State Key Laboratory of Tree Genetics and Breeding (Northeast Forestry University), Harbin, 150040, China.
Zhongyuan Liu *State Key Laboratory of Tree Genetics and Breeding (Northeast Forestry University), Harbin, 150040, China.
Qingjun Xie *State Key Laboratory of Tree Genetics and Breeding (Northeast Forestry University), Harbin, 150040, China.
Jiaru FangState Key Laboratory of Tree Genetics and Breeding (Northeast Forestry University), Harbin, 150040, China.
Chunyao WangState Key Laboratory of Tree Genetics and Breeding (Northeast Forestry University), Harbin, 150040, China.
Jinghang LiState Key Laboratory of Tree Genetics and Breeding (Northeast Forestry University), Harbin, 150040, China.
Chao WangState Key Laboratory of Tree Genetics and Breeding (Northeast Forestry University), Harbin, 150040, China.
Caiqiu GaoState Key Laboratory of Tree Genetics and Breeding (Northeast Forestry University), Harbin, 150040, China. gaocaiqiu@nefu.edu.cn.ORCID http://orcid.org/0000-0001-9953-9775
Northeast Forestry University · CN

Funding

Heilongjiang Touyan Innovation Team Program Breeding Innovation TeamHeilongjiang Touyan Innovation Team Program Tree GeneticsThe National Key Research and Development Program of China 2016YFD0600106
6 · The paper itself

Abstract

key messageConstruction of ML-hGRN for the salt pathway in Populus davidiana × P. bolleana. Construction of ML-hGRN for the lignocellulosic pathway in Populus davidiana × P. bolleana under salt stress. Many woody plants, including Populus davidiana × P. bolleana, have made great contributions to human production and life. High salt is one of the main environmental factors that restricts the growth of poplar. This study found that high salt could induce strong biochemical changes in poplar. To detect the effect of salt treatment on gene expression, 18 libraries were sequenced on the Illumina sequencing platform. The results identified a large number of early differentially expressed genes (DEGs) and a small number of late DEGs, which indicated that most of the salt response genes of poplar were early response genes. In addition, 197 TFs, including NAC, ERF, and other TFs related to salt stress, were differentially expressed during salt treatment, which indicated that these TFs may play an important role in the salt stress response of poplar. Based on the RNA-seq analysis results, multilayered hierarchical gene regulatory networks (ML-hGRNs) of salt stress- and lignocellulosic synthesis-related DEGs were constructed using the GGM algorithm. The lignocellulosic synthesis regulatory network under salt stress revealed that lignocellulosic synthesis might play an important role in the process of salt stress resistance. Furthermore, the NAC family transcription factor PdbNAC83, which was found in the upper layer in both pathways, was selected to verify the accuracy of the ML-hGRNs. DAP-seq showed that the binding site of PdbNAC83 included a "TT(G/A)C(G/T)T" motif, and ChIP-PCR further verified that PdbNAC83 can regulate the promoters of at least six predicted downstream genes (PdbNLP2-2, PdbZFP6, PdbMYB73, PdbC2H2-like, PdbMYB93-1, PdbbHLH094) by binding to the "TT(G/A)C(G/T)T" motif, which indicates that the predicted regulatory network diagram obtained in this study is relatively accurate. In conclusion, a species-specific salt response pathway might exist in poplar, and this finding lays a foundation for further study of the regulatory mechanism of the salt stress response and provides new clues for the use of genetic engineering methods to create high-quality and highly resistant forest germplasms.

Indexed as

PopulusGene Expression ProfilingGene Expression Regulation, PlantHumansLigninSalt StressTranscriptomeLigninlignocelluloseChIP-PCRDAP-SeqML-hGRNsPopulus davidiana × P. bolleanaSalt responseTranscriptome

Identifiers

PMID35486290
OpenAlexW4225150571

What OpenQuestion holds

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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.