Evidence map›Paper›PMID 31203412›Full record

ArticleArchives of toxicology2019

Combined transcriptomic and proteomic analysis reveals a diversity of venom-related and toxin-like peptides expressed in the mat anemone Zoanthus natalensis (Cnidaria, Hexacorallia).

Qiwen Liao, Guiyi Gong, Terence C W Poon, Irene L Ang, Kate M K Lei, Shirley Weng In Siu, Clarence Tsun Ting Wong, Gandhi Rádis-Baptista, Simon Ming-Yuen Lee

Abstract read
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In one paragraph

Article in Archives of toxicology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

  1. Review
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  8. TRPV1 Modulator Ameliorates Alzheimer-Like Amyloid-Oxidative medicine and cellular longevity · 2022
    Article
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  10. Review
  11. 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

9 authors.

Qiwen LiaoState Key Laboratory of Quality Research in Chinese Medicine and Institute of Chinese Medical Sciences, University of Macau, Macau, China.
Guiyi GongState Key Laboratory of Quality Research in Chinese Medicine and Institute of Chinese Medical Sciences, University of Macau, Macau, China.
Terence C W PoonPilot Laboratory and Proteomics Core, Faculty of Health Sciences, University of Macau, Macau, China.
Irene L AngPilot Laboratory and Proteomics Core, Faculty of Health Sciences, University of Macau, Macau, China.
Kate M K LeiPilot Laboratory and Proteomics Core, Faculty of Health Sciences, University of Macau, Macau, China.
Shirley Weng In SiuDepartment of Computer and Information Science, Faculty of Science and Technology, University of Macau, Macau, China.
Clarence Tsun Ting WongDepartment of Chemistry, The Chinese University of Hong Kong, Shatin, Hong Kong, China.
Gandhi Rádis-BaptistaLaboratory of Biochemistry and Biotechnology, Institute for Marine Sciences, Federal University of Ceará, Fortaleza, Brazil.
Simon Ming-Yuen LeeState Key Laboratory of Quality Research in Chinese Medicine and Institute of Chinese Medical Sciences, University of Macau, Macau, China. simonlee@umac.mo.

Funding

Fundo para o Desenvolvimento das Ciências e da Tecnologia No. 069/2015/A2Fundo para o Desenvolvimento das Ciências e da Tecnologia No. 134/2014/A3Universidade de Macau MYRG2015-00182-ICMS-QRCMUniversidade de Macau MYRG2016-00129-ICMS-QRCMUniversidade de Macau MYRG2016-00133-ICMS-QRCM
6 · The paper itself

Abstract

Venoms from marine animals have been recognized as a new emerging source of peptide-based therapeutics. Several peptide toxins from sea anemone have been investigated as therapeutic leads or pharmacological tools. Venom complexity should be further highlighted using combined strategies of large-scale sequencing and data analysis which integrated transcriptomics and proteomics to elucidate new proteins or peptides to be compared among species. In this work, transcriptomic and proteomic analyses were combined to identify six groups of expressed peptide toxins in Zoanthus natalensis. These include neurotoxin, hemostatic and hemorrhagic toxin, protease inhibitor, mixed function enzymes, venom auxiliary proteins, allergen peptides, and peptides related to the innate immunity. Molecular docking analysis indicated that one expressed Zoanthus Kunitz-like peptide, ZoaKuz1, could be a voltage-gated potassium channels blocker and, hence, it was selected for functional studies. Functional bioassays revealed that ZoaKuz1 has an intrinsic neuroprotective activity in zebrafish model of Parkinson's disease. Since pharmacological blockade of K

Indexed as

ProteomicsTranscriptomeAllergensAnimalsAntiparkinson AgentsCnidarian VenomsHemostaticsHumansMolecular Docking SimulationNeuroprotective AgentsNeurotoxinsPeptidesPotassium Channel BlockersProtease InhibitorsProtein FoldingSea AnemonesAllergensAntiparkinson AgentsCnidarian VenomsHemostaticsNeuroprotective AgentsNeurotoxinsPeptidesPotassium Channel BlockersProtease InhibitorsCnidariaNeuroprotectionProteomicTranscriptomicVenom-derived peptideZoantharian

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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.