Evidence map›Paper›PMID 29881386›Full record

ArticleFrontiers in immunology2018

Ancient Origin of the CARD-Coiled Coil/Bcl10/MALT1-Like Paracaspase Signaling Complex Indicates Unknown Critical Functions.

Jens Staal, Yasmine Driege, Mira Haegman, Alice Borghi, Paco Hulpiau, Laurens Lievens, Ismail Sahin Gul, Srividhya Sundararaman, Amanda Gonçalves, Ineke Dhondt and 6 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

17 citing papers in PubMed, 31 citations in OpenAlex.

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  4. The role of the CBM complex in allergic inflammation and disease.The Journal of allergy and clinical immunology · 2022
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  17. AFrontiers in immunology · 2018
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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

16 authors at 4 institutions in 3 countries.

Jens StaalUnit of Molecular Signal Transduction in Inflammation, VIB-UGent Center for Inflammation Research (IRC), Ghent, Belgium.
Yasmine DriegeUnit of Molecular Signal Transduction in Inflammation, VIB-UGent Center for Inflammation Research (IRC), Ghent, Belgium.
Mira HaegmanUnit of Molecular Signal Transduction in Inflammation, VIB-UGent Center for Inflammation Research (IRC), Ghent, Belgium.
Alice BorghiUnit of Molecular Signal Transduction in Inflammation, VIB-UGent Center for Inflammation Research (IRC), Ghent, Belgium.
Paco HulpiauDepartment of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.
Laurens LievensUnit of Molecular Signal Transduction in Inflammation, VIB-UGent Center for Inflammation Research (IRC), Ghent, Belgium.
Ismail Sahin GulDepartment of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.
Srividhya SundararamanDepartment of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.
Amanda GonçalvesDepartment of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.
Ineke DhondtLaboratory for Aging Physiology and Molecular Evolution, Biology Department, Ghent University, Ghent, Belgium.
Jorge H PinzónDepartment of Biology, University of Texas Arlington, Arlington, TX, United States.
Bart P BraeckmanLaboratory for Aging Physiology and Molecular Evolution, Biology Department, Ghent University, Ghent, Belgium.
Ulrich TechnauDepartment of Molecular Evolution and Development, Faculty of Life Sciences, University of Vienna, Vienna, Austria.
Yvan SaeysUnit of Data Mining and Modeling for Biomedicine, VIB-UGent Center for Inflammation Research (IRC), Ghent, Belgium.
Frans van RoyDepartment of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.
Rudi BeyaertUnit of Molecular Signal Transduction in Inflammation, VIB-UGent Center for Inflammation Research (IRC), Ghent, Belgium.
Ghent University · BEVIB-UGent Center for Inflammation Research · BEThe University of Texas at Arlington · USUniversity of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The CARD-coiled coil (CC)/Bcl10/MALT1-like paracaspase (CBM) signaling complexes composed of a CARD-CC family member (CARD-9, -10, -11, or -14), Bcl10, and the type 1 paracaspase MALT1 (PCASP1) play a pivotal role in immunity, inflammation, and cancer. Targeting MALT1 proteolytic activity is of potential therapeutic interest. However, little is known about the evolutionary origin and the original functions of the CBM complex. Type 1 paracaspases originated before the last common ancestor of planulozoa (bilaterians and cnidarians). Notably in bilaterians, Ecdysozoa (e.g., nematodes and insects) lacks Bcl10, whereas other lineages have a Bcl10 homolog. A survey of invertebrate CARD-CC homologs revealed such homologs only in species with Bcl10, indicating an ancient common origin of the entire CBM complex. Furthermore, vertebrate-like Syk/Zap70 tyrosine kinase homologs with the ITAM-binding SH2 domain were only found in invertebrate organisms with CARD-CC/Bcl10, indicating that this pathway might be related to the original function of the CBM complex. Moreover, the type 1 paracaspase sequences from invertebrate organisms that have CARD-CC/Bcl10 are more similar to vertebrate paracaspases. Functional analysis of protein-protein interactions, NF-κB signaling, and CYLD cleavage for selected invertebrate type 1 paracaspase and Bcl10 homologs supports this scenario and indicates an ancient origin of the CARD-CC/Bcl10/paracaspase signaling complex. By contrast, many of the known MALT1-associated activities evolved fairly recently, indicating that unknown functions are at the basis of the protein conservation. As a proof-of-concept, we provide initial evidence for a CBM- and NF-κB-independent neuronal function of the Caenorhabditis elegans type 1 paracaspase malt-1. In conclusion, this study shows how evolutionary insights may point at alternative functions of MALT1.

Indexed as

Signal TransductionAnimalsB-Cell CLL-Lymphoma 10 ProteinBiological EvolutionCARD Signaling Adaptor ProteinsCaspasesCell LineHumansMucosa-Associated Lymphoid Tissue Lymphoma Translocation 1 ProteinMultiprotein ComplexesNF-kappa BProtein BindingProteolysisSea AnemonesVertebratesB-Cell CLL-Lymphoma 10 ProteinCARD Signaling Adaptor ProteinsCaspasesMucosa-Associated Lymphoid Tissue Lymphoma Translocation 1 ProteinMultiprotein ComplexesNF-kappa BCaenorhabditis eleganscoral bleachingmolecular evolutionNematostella vectensisNF-kappaBprotein–protein interactionsignal transductionstructure–function analysis

Identifiers

PMID29881386
PMCPMC5978004
OpenAlexW2802588814

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.