Evidence map›Paper›PMID 41015904›Full record

ReviewJournal of cellular physiology2025

Holding Out for a Model: Rhomboid Superfamily in Vertebrate Development and Disease.

Saroj Gourkanti, Yazmin Munoz, Jacqueline Cheung, Rosa M Chavez, Devanshi Agarwal, Taylor J Schoen, Kristina Solorio-Kirpichyan, Sonya E Neal

Abstract readReview
In one paragraph

Review in Journal of cellular physiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Proteolytic control of mitochondrial protein translocases.Protein science : a publication of the Protein Society · 2026
    Review
  3. 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

8 authors.

Saroj GourkantiDepartment of Cell and Developmental Biology, School of Biological Sciences, University of California San Diego, San Diego, California, USA.
Yazmin MunozDepartment of Cell and Developmental Biology, School of Biological Sciences, University of California San Diego, San Diego, California, USA.
Jacqueline CheungDepartment of Cell and Developmental Biology, School of Biological Sciences, University of California San Diego, San Diego, California, USA.
Rosa M ChavezDepartment of Cell and Developmental Biology, School of Biological Sciences, University of California San Diego, San Diego, California, USA.
Devanshi AgarwalDepartment of Cell and Developmental Biology, School of Biological Sciences, University of California San Diego, San Diego, California, USA.
Taylor J SchoenDepartment of Cell and Developmental Biology, School of Biological Sciences, University of California San Diego, San Diego, California, USA.
Kristina Solorio-KirpichyanDepartment of Cell and Developmental Biology, School of Biological Sciences, University of California San Diego, San Diego, California, USA.
Sonya E NealDepartment of Cell and Developmental Biology, School of Biological Sciences, University of California San Diego, San Diego, California, USA.

Funding

UCSD/SDSU IRACDAK12GM068524 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI TREJO, JOANN · 2003 to 2025
$24.4M
The Discovery of Molecules and Mechanisms of the Rhomboid SuperfamilyR35GM133565 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Sonya Elina Neal · 2019 to 2026
$2.9M
NIGMS NIH HHS K12 GM068524NIGMS NIH HHS R35 GM133565
6 · The paper itself

Abstract

The rhomboid superfamily, comprising both proteases and pseudoproteases, has emerged as a central regulator of membrane biology, mediating diverse functions including protein quality control, signal transduction, trafficking, and more. While molecular mechanisms of rhomboid activity have been well-characterized in invertebrate and cell-based systems, their physiological role in vertebrate development remains limited and continues to evolve. Here, we review recent advances in cell culture systems and vertebrate models that uncover the developmental and disease-relevant functions of rhomboid family members, including RHBDLs, iRhoms, PARL, and Derlins. We outline their roles in embryogenesis, tissue regeneration, neurodevelopment, and immune signaling, alongside their pathological involvement in cancer, neurodegeneration, and metabolic disorders. We also emphasize the limitations posed by early embryonic lethality in knockout models and advocate for tissue-specific vertebrate models to dissect rhomboid-dependent pathways in vivo. Understanding how rhomboid proteins coordinate developmental processes will not only reveal fundamental principles of membrane-associated processes, but also open new avenues for therapeutic targeting in disease.

Indexed as

Embryonic DevelopmentMembrane ProteinsVertebratesAnimalsHumansSignal TransductionMembrane Proteinsdevelopmentmembranerhomboid proteinsvertebrate model

Identifiers

PMID41015904
PMCPMC12476590

What OpenQuestion holds

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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.