Evidence map›Paper›PMID 29227022›Full record

ArticleMolecular plant pathology2018

The GATA-type IVb zinc-finger transcription factor SsNsd1 regulates asexual-sexual development and appressoria formation in Sclerotinia sclerotiorum.

Jingtao Li, Wenhui Mu, Selvakumar Veluchamy, Yanzhi Liu, Yanhua Zhang, Hongyu Pan, Jeffrey A Rollins

Open access · bronzeAbstract read
In one paragraph

Article in Molecular plant pathology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
11.7field-weighted citation impact, top 2% 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

37 citing papers in PubMed, 68 citations in OpenAlex.

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  14. An Amidase Contributes to Full Virulence ofInternational journal of molecular sciences · 2022
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  18. ε-poly-Journal of fungi (Basel, Switzerland) · 2021
    Article
  19. Diversity and Function of Appressoria.Pathogens (Basel, Switzerland) · 2021
    Review
  20. Article
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

7 authors at 2 institutions in 2 countries.

Jingtao LiDepartment of Plant Pathology, University of Florida, Gainesville, FL 32611, USA.
Wenhui MuDepartment of Plant Pathology, University of Florida, Gainesville, FL 32611, USA.
Selvakumar VeluchamyDepartment of Plant Pathology, University of Florida, Gainesville, FL 32611, USA.
Yanzhi LiuCollege of Plant Science, Jilin University, Changchun, Jilin Province, 130062, China.
Yanhua ZhangDepartment of Plant Pathology, University of Florida, Gainesville, FL 32611, USA.
Hongyu PanCollege of Plant Science, Jilin University, Changchun, Jilin Province, 130062, China.
Jeffrey A RollinsDepartment of Plant Pathology, University of Florida, Gainesville, FL 32611, USA.ORCID 0000-0002-9897-6292
Jilin University · CNUniversity of Florida · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The sclerotium, a multicellular structure composed of the compact aggregation of vegetative hyphae, is critical for the long-term survival and sexual reproduction of the plant-pathogenic fungus Sclerotinia sclerotiorum. The development and carpogenic germination of sclerotia are regulated by integrating signals from both environmental and endogenous processes. Here, we report the regulatory functions of the S. sclerotiorum GATA-type IVb zinc-finger transcription factor SsNsd1 in these processes. SsNsd1 is orthologous to the Aspergillus nidulans NsdD (never in sexual development) and the Neurospora crassa SUB-1 (submerged protoperithecia-1) proteins. Ssnsd1 gene transcript accumulation remains relatively low, but variable, during vegetative mycelial growth and multicellular development. Ssnsd1 deletion mutants (Δnsd1-KOs) produce phialides and phialospores (spermatia) excessively in vegetative hyphae and promiscuously within the interior medulla of sclerotia. In contrast, phialospore development occurs only on the sclerotium surface in the wild-type. Loss of SsNsd1 function affects sclerotium structural integrity and disrupts ascogonia formation during conditioning for carpogenic germination. As a consequence, apothecium development is abolished. The Ssnsd1 deletion mutants are also defective in the transition from hyphae to compound appressorium formation, resulting in a loss of pathogenicity on unwounded hosts. In sum, our results demonstrate that SsNsd1 functions in a regulatory role similar to its ascomycete orthologues in regulating sexual and asexual development. Further, SsNsd1 appears to have evolved as a regulator of pre-penetration infectious development required for the successful infection of its many hosts.

Indexed as

AscomycotaFungal ProteinsGene Expression Regulation, FungalTranscription FactorsFungal ProteinsTranscription Factorsappressoriumasexual developmentNsdDsexual developmentspermatia

Identifiers

PMID29227022
PMCPMC6638148
OpenAlexW2772769731

What OpenQuestion holds

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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.