Evidence map›Paper›PMID 40892950›Full record

ArticlePloS one2025

KFERQ-selective protein autophagy in Caenorhabditis elegans depends on LMP-1.

María Gallardo-Campos, Alicia N Minniti, Juan Hormazabal, Gonzalo Núñez, Carlos F Lagos, Tomás Perez-Acle, Rebeca Aldunate, Iván E Alfaro

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Autophagy: A Double-Edged Sword in the Aging ofInternational journal of molecular sciences · 2026
    Review
  2. Crosstalk Between Allergic Inflammation and Autophagy.International journal of molecular sciences · 2025
    Review
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

8 authors.

María Gallardo-CamposEscuela de Biotecnología, Facultad de Ciencias, Universidad Santo Tomás, Santiago, Chile.ORCID https://orcid.org/0009-0001-3965-7718
Alicia N MinnitiFacultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.
Juan HormazabalInstituto de Ciencias e Innovación en Medicina, Facultad de Medicina Clínica Alemana Universidad del Desarrollo, Santiago, Chile.ORCID https://orcid.org/0000-0003-0726-2778
Gonzalo NúñezInstituto de Ciencias e Innovación en Medicina, Facultad de Medicina Clínica Alemana Universidad del Desarrollo, Santiago, Chile.ORCID https://orcid.org/0000-0002-6698-1732
Carlos F LagosChemical Biology & Drug Discovery Lab, Escuela de Química y Farmacia, Facultad de Medicina y Ciencias, Universidad San Sebastián, Campus Los Leones, Santiago, Chile.ORCID https://orcid.org/0000-0002-5432-9747
Tomás Perez-AcleCentro Ciencia & Vida, Fundación Ciencia & Vida, Santiago, Chile.ORCID https://orcid.org/0000-0002-3769-390X
Rebeca AldunateEscuela de Biotecnología, Facultad de Ciencias, Universidad Santo Tomás, Santiago, Chile.ORCID https://orcid.org/0000-0002-5540-3187
Iván E AlfaroInstituto de Ciencias e Innovación en Medicina, Facultad de Medicina Clínica Alemana Universidad del Desarrollo, Santiago, Chile.

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
NIH HHS P40 OD010440
6 · The paper itself

Abstract

Mammalian cells exhibit three autophagy mechanisms: macroautophagy, microautophagy (MIA), and chaperone-mediated autophagy (CMA), each employing unique mechanisms for transporting cellular material to the lysosome for degradation. MIA involves the engulfment of proteins via lysosomes/late endosomes through membrane invagination, while CMA directly imports cytosolic proteins into lysosomes, selectively targeting those harboring the KFERQ pentapeptide motif, helped by the chaperone HSC70. Despite the identification of several genetic markers of these pathways, our understanding of the underlying mechanisms, particularly in MIA and CMA, remains limited. To study CMA in vivo we designed a photoactivatable CMA reporter consisting of a plasmid encoding the KFERQ consensus signal for CMA targeting. We generated transgenic C. elegans strains with diverse genetic backgrounds to analyze the role of known molecular components of CMA in mammals. Additionally, we conducted an in-silico analysis of the structural interaction between C. elegans LMP-1 or LMP-2 proteins with the HSP-1 chaperone. Results: Our study shows a significant alteration in the distribution pattern of the KFERQ reporter in muscle cells upon induction of selective autophagy (CMA or MIA). We found that the reporter localized into lysosomes only during starvation, which abrogated in the absence of LMP-1. This study validates CMA in C. elegans and provides the development of a new tool for understanding selective autophagy mechanisms and their potential implications in various organisms.

Indexed as

AutophagyCaenorhabditis elegansCaenorhabditis elegans ProteinsChaperone-Mediated AutophagyAnimalsAnimals, Genetically ModifiedHSC70 Heat-Shock ProteinsLysosomesCaenorhabditis elegans ProteinsHSC70 Heat-Shock Proteins

Identifiers

PMID40892950
PMCPMC12404552

What OpenQuestion holds

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LicenceCC BY
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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.