Evidence map›Paper›PMID 40424258›Full record

ArticlePLoS biology2025

An animal toxin-antidote system kills cells by creating a novel cation channel.

Lews Caro, Aguan D Wei, Christopher A Thomas, Galen Posch, Ahmet Uremis, Michaela C Franzi, Sarah J Abell, Andrew H Laszlo, Jens H Gundlach, Jan-Marino Ramirez and 1 more

Abstract read
In one paragraph

Article in PLoS biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Parental-effect gene-drive elements under partial selfing, or why dobioRxiv : the preprint server for biology · 2024
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Lews CaroMolecular and Cellular Biology Ph.D. Program, University of Washington, Seattle, Washington, United States of America.
Aguan D WeiNorcliffe Foundation Center for Integrative Brain Research, Seattle Children's Research Institute, Seattle, Washington, United States of America.
Christopher A ThomasDepartment of Physics, University of Washington, Seattle, Washington, United States of America.
Galen PoschDepartment of Biochemistry, University of Washington, Seattle, Washington, United States of America.
Ahmet UremisDepartment of Biochemistry, University of Washington, Seattle, Washington, United States of America.
Michaela C FranziDepartment of Physics, University of Washington, Seattle, Washington, United States of America.
Sarah J AbellDepartment of Physics, University of Washington, Seattle, Washington, United States of America.
Andrew H LaszloDepartment of Physics, University of Washington, Seattle, Washington, United States of America.
Jens H GundlachDepartment of Physics, University of Washington, Seattle, Washington, United States of America.
Jan-Marino RamirezNorcliffe Foundation Center for Integrative Brain Research, Seattle Children's Research Institute, Seattle, Washington, United States of America.
Michael AilionMolecular and Cellular Biology Ph.D. Program, University of Washington, Seattle, Washington, United States of America.ORCID 0000-0002-8070-1362

Funding

TRAINING IN MOLECULAR AND CELLULAR BIOLOGYT32GM007270 · NIGMS · UNIVERSITY OF WASHINGTON · PI RAIBLE, DAVID W · 1985 to 2020
$21.0M
Nanopore sequencing of DNA with MspAR01HG005115 · NHGRI · UNIVERSITY OF WASHINGTON · PI GUNDLACH, JENS, LASZLO, ANDREW · 2009 to 2024
$14.0M
Unraveling respiratory rhythm generation in the medullary networkR01HL126523 · NHLBI · SEATTLE CHILDREN'S HOSPITAL · PI Jan M. Ramirez · 2015 to 2026
$8.3M
Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
Unraveling the dynamic mechanisms underlying opioid respiratory depressionR01HL144801 · NHLBI · SEATTLE CHILDREN'S HOSPITAL · PI Jan M. Ramirez · 2019 to 2026
$5.2M
Neuroglial interactions underlying the generation of the sighR01HL151389 · NHLBI · SEATTLE CHILDREN'S HOSPITAL · PI RAMIREZ, JAN M. · 2020 to 2023
$3.2M
NHGRI NIH HHS R01 HG005115NHLBI NIH HHS R01 HL126523NHLBI NIH HHS R01 HL144801NHLBI NIH HHS R01 HL151389NIGMS NIH HHS T32 GM007270NIH HHS P40 OD010440
6 · The paper itself

Abstract

Toxin-antidote systems are selfish genetic elements composed of a linked toxin and antidote. The peel-1 zeel-1 toxin-antidote system in C. elegans consists of a transmembrane toxin protein PEEL-1 which acts cell autonomously to kill cells. Here we investigate the molecular mechanism of PEEL-1 toxicity. We find that PEEL-1 requires a small membrane protein, PMPL-1, for toxicity. Together, PEEL-1 and PMPL-1 are sufficient for toxicity in a heterologous system, HEK293T cells, and cause cell swelling and increased cell permeability to monovalent cations. Using purified proteins, we show that PEEL-1 and PMPL-1 allow ion flux through lipid bilayers and generate currents which resemble ion channel gating. Our work suggests that PEEL-1 kills cells by co-opting PMPL-1 and creating a cation channel.

Indexed as

Caenorhabditis elegansCaenorhabditis elegans ProteinsIon ChannelsToxins, BiologicalAnimalsCationsHEK293 CellsHumansIon Channel GatingLipid BilayersCaenorhabditis elegans ProteinsCationsIon ChannelsLipid BilayersToxins, Biological

Identifiers

PMID40424258
PMCPMC12136403

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.