Evidence map›Paper›PMID 40107406›Full record

ReviewArchives of biochemistry and biophysics2025

Insights from selenoprotein I mouse models for understanding biological roles of this enzyme.

Lance G A Nunes, Chi Ma, Matthew W Pitts, Peter R Hoffmann

Abstract readReview
In one paragraph

Review in Archives of biochemistry and biophysics, 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. Review
  2. 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

4 authors.

Lance G A NunesDepartment of Cell and Molecular Biology, John A. Burns School of Medicine, University of Hawaii, Honolulu, HI, 96813, USA.
Chi MaDepartment of Cell and Molecular Biology, John A. Burns School of Medicine, University of Hawaii, Honolulu, HI, 96813, USA.
Matthew W PittsDepartment of Cell and Molecular Biology, John A. Burns School of Medicine, University of Hawaii, Honolulu, HI, 96813, USA.
Peter R HoffmannDepartment of Cell and Molecular Biology, John A. Burns School of Medicine, University of Hawaii, Honolulu, HI, 96813, USA. Electronic address: peterrh@hawaii.edu.

Funding

UH Hilo COP A&RP20GM103466 · NIGMS · UNIVERSITY OF HAWAII AT MANOA · PI Peter R Hoffmann · 2012 to 2026
$60.3M
Selenoprotein K modulates calcium-dependent signaling in immune cellsR01AI089999 · NIAID · UNIVERSITY OF HAWAII AT MANOA · PI HOFFMANN, PETER R · 2010 to 2020
$3.6M
The Role of Selenoprotein I in Phospholipidethanolamine Dependent Mechanisms that Regulate T Cell ActivationR01AI147496 · NIAID · UNIVERSITY OF HAWAII AT MANOA · PI HOFFMANN, PETER R · 2019 to 2023
$2.1M
Assessment of the joint influence of methylmercury and selenium upon postnatal brain development and risk for psychiatric disordersR01ES035851 · NIEHS · UNIVERSITY OF HAWAII AT MANOA · PI Matthew William Pitts · 2024 to 2026
$1.2M
The role of Selenoprotein I in mitigating neurodegeneration.R21NS133944 · NINDS · UNIVERSITY OF HAWAII AT MANOA · PI HOFFMANN, PETER R, PITTS, MATTHEW WILLIAM · 2023 to 2023
$430k
Mechanisms by which selenium influences T helper cells during immune responsesR21AT004844 · NCCIH · UNIVERSITY OF HAWAII AT MANOA · PI HOFFMANN, PETER R · 2009 to 2010
$411k
NCCIH NIH HHS R21 AT004844NIAID NIH HHS R01 AI089999NIAID NIH HHS R01 AI147496NIEHS NIH HHS R01 ES035851NIGMS NIH HHS P20 GM103466NINDS NIH HHS R21 NS133944
6 · The paper itself

Abstract

Selenoprotein I (selenoi) is a metabolic enzyme expressed in a wide variety of tissues that catalyzes the transfer of the ethanolamine phosphate group from CDP-ethanolamine to lipid acceptors to generate ethanolamine phospholipids. It is a member of the selenoprotein family, a class of proteins that mostly play fundamental roles in redox homeostasis and are defined by the co-translational incorporation of selenium in the form of selenocysteine. Loss-of-function mutations in the human SELENOI gene have been found in rare cases leading to a complex form of hereditary spastic paraplegia. Understanding the roles of this selenoprotein and its phospholipid products in different cell types has benefited from the development of mouse models. In particular, global and conditional knockout (KO) of the Selenoi gene in mice has enabled a more complete picture to emerge of how this important selenoprotein is integrated into metabolic pathways. These data have revealed how Selenoi loss-of-function affects embryogenesis, neurodevelopment, the immune system and liver physiology. This review summarizes the insights gained through mouse model experiments and the current understanding the different physiological roles played by this selenoprotein.

Indexed as

SelenoproteinsAnimalsHumansMiceMice, KnockoutSelenoproteinsEthanolamine phospholipid transferaseMetabolismPhosphatidylethanolaminePlasmalogenPlasmenyl-PE

Identifiers

PMID40107406
PMCPMC11994276

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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.