Evidence map›Paper›PMID 33494703›Full record

ArticleBMC genomics2021

Phylogenetic analysis of the caspase family in bivalves: implications for programmed cell death, immune response and development.

Susanne Vogeler, Stefano Carboni, Xiaoxu Li, Alyssa Joyce

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
4.5field-weighted citation impact, top 4% 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

22 citing papers in PubMed, 60 citations in OpenAlex.

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  16. Programmed Cell Death in Diabetic Nephropathy: A Review of Apoptosis, Autophagy, and Necroptosis.Medical science monitor : international medical journal of experimental and clinical research · 2022
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  20. Effects ofThe Journal of international medical research · 2022
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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

4 authors at 3 institutions in 3 countries.

Susanne VogelerDepartment of Marine Science, University of Gothenburg, Carl Skottbergsgata 22 B, 41319, Gothenburg, Sweden.
Stefano CarboniInstitute of Aquaculture, University of Stirling, Stirling, Scotland, FK9 4LA, UK.
Xiaoxu LiSouth Australia Research and Development Institute Aquatic Sciences Centre, 2 Hamra Ave, West Beach, SA, 5024, Australia.
Alyssa JoyceDepartment of Marine Science, University of Gothenburg, Carl Skottbergsgata 22 B, 41319, Gothenburg, Sweden. alyssa.joyce@marine.gu.se.
University of Gothenburg · SESouth Australian Research and Development Institute · AUUniversity of Stirling · GB

Funding

AquaExcel 2020 AE120009Svenska Forskningsrådet Formas Joyce 2015-1484
6 · The paper itself

Abstract

backgroundApoptosis is an important process for an organism's innate immune system to respond to pathogens, while also allowing for cell differentiation and other essential life functions. Caspases are one of the key protease enzymes involved in the apoptotic process, however there is currently a very limited understanding of bivalve caspase diversity and function.

resultsIn this work, we investigated the presence of caspase homologues using a combination of bioinformatics and phylogenetic analyses. We blasted the Crassostrea gigas genome for caspase homologues and identified 35 potential homologues in the addition to the already cloned 23 bivalve caspases. As such, we present information about the phylogenetic relationship of all identified bivalve caspases in relation to their homology to well-established vertebrate and invertebrate caspases. Our results reveal unexpected novelty and complexity in the bivalve caspase family. Notably, we were unable to identify direct homologues to the initiator caspase-9, a key-caspase in the vertebrate apoptotic pathway, inflammatory caspases (caspase-1, - 4 or - 5) or executioner caspases-3, - 6, - 7. We also explored the fact that bivalves appear to possess several unique homologues to the initiator caspase groups - 2 and - 8. Large expansions of caspase-3 like homologues (caspase-3A-C), caspase-3/7 group and caspase-3/7-like homologues were also identified, suggesting unusual roles of caspases with direct implications for our understanding of immune response in relation to common bivalve diseases. Furthermore, we assessed the gene expression of two initiator (Cg2A, Cg8B) and four executioner caspases (Cg3A, Cg3B, Cg3C, Cg3/7) in C. gigas late-larval development and during metamorphosis, indicating that caspase expression varies across the different developmental stages.

conclusionOur analysis provides the first overview of caspases across different bivalve species with essential new insights into caspase diversity, knowledge that can be used for further investigations into immune response to pathogens or regulation of developmental processes.

Indexed as

ApoptosisCaspasesAnimalsCaspase 7ImmunityPhylogenyCaspase 7CaspasesApoptosisBivalvesCaspaseInflammation responseInnate immune systemProgrammed cell deathPyroptosis

Identifiers

PMID33494703
PMCPMC7836458
OpenAlexW3122885492

What OpenQuestion holds

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LicenceCC BY
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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.