Evidence map›Paper›PMID 32572596›Full record

ArticleCurrent genetics2020

Two mating-type genes MAT1-1-1 and MAT1-1-2 with significant functions in conidiation, stress response, sexual development, and pathogenicity of rice false smut fungus Villosiclava virens.

Mingli Yong, Junjie Yu, Xiayan Pan, Mina Yu, Huijuan Cao, Tianqiao Song, Zhongqiang Qi, Yan Du, Rongsheng Zhang, Xiaole Yin and 2 more

Abstract read
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In one paragraph

Article in Current genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

10 citing papers in PubMed, 18 citations in OpenAlex.

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  7. Assessing thermal adaptation of a global sample ofFrontiers in public health · 2023
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  8. Truncation ofMicrobiology spectrum · 2022
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  9. TheFrontiers in fungal biology · 2022
    Article
  10. Genetic Networks That Govern Sexual Reproduction in the Pezizomycotina.Microbiology and molecular biology reviews : MMBR · 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

12 authors at 2 institutions in 1 country.

Mingli YongInstitute of Plant Protection, Jiangsu Academy of Agricultural Sciences, Nanjing, China.
Junjie YuInstitute of Plant Protection, Jiangsu Academy of Agricultural Sciences, Nanjing, China.
Xiayan PanInstitute of Plant Protection, Jiangsu Academy of Agricultural Sciences, Nanjing, China.
Mina YuInstitute of Plant Protection, Jiangsu Academy of Agricultural Sciences, Nanjing, China.
Huijuan CaoInstitute of Plant Protection, Jiangsu Academy of Agricultural Sciences, Nanjing, China.
Tianqiao SongInstitute of Plant Protection, Jiangsu Academy of Agricultural Sciences, Nanjing, China.
Zhongqiang QiInstitute of Plant Protection, Jiangsu Academy of Agricultural Sciences, Nanjing, China.
Yan DuInstitute of Plant Protection, Jiangsu Academy of Agricultural Sciences, Nanjing, China.
Rongsheng ZhangInstitute of Plant Protection, Jiangsu Academy of Agricultural Sciences, Nanjing, China.
Xiaole YinInstitute of Plant Protection, Jiangsu Academy of Agricultural Sciences, Nanjing, China.
Wende LiuState Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing, China.
Yongfeng LiuInstitute of Plant Protection, Jiangsu Academy of Agricultural Sciences, Nanjing, China. liuyf@jaas.ac.cn.ORCID http://orcid.org/0000-0003-3583-8092
Jiangsu Academy of Agricultural Sciences · CNInstitute of Plant Protection · CN

Funding

National Natural Science Foundation of China No. 31571961Postdoctoral Research Foundation of China 2018M632257
6 · The paper itself

Abstract

Rice false smut caused by Villosiclava virens is one of the destructive diseases on panicles of rice. Sexual development of V. virens, controlled by mating-type locus, plays an important role in the prevalence of rice false smut and genetic diversity of the pathogen. However, how the mating-type genes mediate sexual development of the V. virens remains largely unknown. In this study, we characterized the two mating-type genes, MAT1-1-1 and MAT1-1-2, in V. virens. MAT1-1-1 knockout mutant showed defects in hyphal growth, conidia morphogenesis, sexual development, and increase in the tolerance to salt and osmotic stress. Targeted deletion of MAT1-1-2 not only impaired the sclerotia formation and pathogenicity of V. virens, but also reduced the production of conidia. The MAT1-1-2 mutant showed increases in tolerance to salt and hydrogen peroxide stress, but decreases in tolerance to osmotic stress. Yeast two-hybrid assay showed that MAT1-1-1 interacted with MAT1-1-2, indicating that those proteins might form a complex to regulate sexual development. In addition, MAT1-1-1 localized in the nucleus, and MAT1-1-2 localized in the cytoplasm. Collectively, our results demonstrate that MAT1-1-1 and MAT1-1-2 play important roles in the conidiation, stress response, sexual development, and pathogenicity of V. virens, thus providing new insights into the function of mating-type gene.

Indexed as

Genes, Mating Type, FungalSexual DevelopmentStress, PhysiologicalHost-Pathogen InteractionsHypocrealesOryzaPlant DiseasesSpores, FungalVirulenceConidiationMating-type genePathogenicitySexual developmentStress responseVillosiclava virens

Identifiers

PMID32572596
OpenAlexW3036502999

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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.