Evidence map›Paper›PMID 32934312›Full record

ArticleScientific reports2020

Analysis of TabZIP15 transcription factor from Trichoderma asperellum ACCC30536 and its function under pathogenic toxin stress.

Zeyang Yu, Zhiying Wang, Yuzhou Zhang, Yucheng Wang, Zhihua Liu

Abstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Zeyang YuSchool of Forestry, Northeast Forestry University, No. 26 Hexing Road, Harbin, 150040, China.
Zhiying WangSchool of Forestry, Northeast Forestry University, No. 26 Hexing Road, Harbin, 150040, China.
Yuzhou ZhangGeneral Station of Forest and Grassland Pest Management, National Forestry and Grassland Administration, No. 58 Huanghe Street, Shenyang, 110034, China.
Yucheng WangSchool of Forestry, Northeast Forestry University, No. 26 Hexing Road, Harbin, 150040, China.
Zhihua LiuSchool of Forestry, Northeast Forestry University, No. 26 Hexing Road, Harbin, 150040, China. LZHNEFU@126.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The TabZIP15 gene encoding a 396 amino acid (aa) polypeptide in the fungus Trichoderma asperellum ACCC30536 was cloned and characterised. The protein includes a basic region motif (NR-x2-QR-x2-R) and has a pillar-like structure. The 25 basic region/leucine zipper transcription factors (TFs) identified in the T. asperellum genome were divided into YAP (14 TFs), ATF2 (5), GCN4 (2), Zip1 (2), BRLZ (1) and u1 (1) subfamilies based on conserved domains. T. asperellum was cultured in minimal media (MM) control, C-Hungry and N-Hungry medium (to simulate nutrient competition and interaction with pathogens, respectively), and differential expression analysis showed that 14 TabZIP genes (including TabZIP15) were significantly altered under both conditions; TabZIP23 responded strongly to N-Hungry media and TabZIP24 responded strongly to C-Hungry media. However, only YAP genes TabZIP15, TabZIP12 and TabZIP2 were significantly upregulated under both conditions, and expression levels of TabZIP15 were highest. T. asperellum was also cultured in the presence of five fungal pathogenic toxins, and RT-qPCR results showed that TabZIP15 was significantly upregulated in four of the five toxin stress conditions (MM + Rhizoctonia solani, MM + Fusarium oxysporum, MM + Alternaria alternata and MM + Cytospora chrysosperma).

Indexed as

AlternariaAscomycotaBacterial ToxinsFungal ProteinsFusariumGene Expression Regulation, FungalGenes, FungalHypocrealesMycotoxinsRhizoctoniaTranscription FactorsUp-RegulationBacterial ToxinsFungal ProteinsMycotoxinsTranscription Factors

Identifiers

PMID32934312
PMCPMC7493895

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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.