Evidence map›Paper›PMID 31595490›Full record

ArticleFEBS letters2020

Impacts of deletion and ichthyosis prematurity syndrome-associated mutations in fatty acid transport protein 4 on the function of RPE65.

Songhua Li, John F Green, Minghao Jin

Open access · bronzeAbstract read
In one paragraph

Article in FEBS letters, 2020. 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
0.2field-weighted citation impact, top 47% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Ablation of Fatty Acid Transport Protein-4 Enhances Cone Survival, M-cone Vision, and Synthesis of Cone-Tropic 9-The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  3. Review
  4. 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

3 authors at 1 institution in 1 country.

Songhua LiNeuroscience Center of Excellence, Louisiana State University School of Medicine, New Orleans, LA, USA.
John F GreenNeuroscience Center of Excellence, Louisiana State University School of Medicine, New Orleans, LA, USA.
Minghao JinNeuroscience Center of Excellence, Louisiana State University School of Medicine, New Orleans, LA, USA.ORCID 0000-0002-6790-8860
Louisiana State University · US

Funding

SYNAPTIC AND EXTRASYNAPTIC NMDA RECEPTORS AND NEUROPROTECTIVE LIPID SIGNALINGP20RR016816 · NCRR · LSU HEALTH SCIENCES CENTER · PI CANAVIER, CARMEN CASTRO · 2002 to 2011
$20.2M
Multiphoton ConfocalP30GM103340 · NIGMS · LSU HEALTH SCIENCES CENTER · PI SHELINE, CHRISTIAN THOMAS · 2012 to 2016
$5.1M
Regulation of normal and Leber congenital amaurosis-associated RPE65sR01EY021208 · NEI · LSU HEALTH SCIENCES CENTER · PI JIN, MINGHAO · 2011 to 2015
$1.7M
Mechanisms that regulate RPE65 isomerase in normal and blindness-associated RPER01EY028572 · NEI · LSU HEALTH SCIENCES CENTER · PI JIN, MINGHAO · 2018 to 2021
$1.5M
NCRR NIH HHS P20 RR016816NEI NIH HHS R01 EY021208NEI NIH HHS R01 EY028572NIGMS NIH HHS P30 GM103340
6 · The paper itself

Abstract

The retinal pigment epithelium-specific 65 kDa (RPE65) isomerase plays a pivotal role in photoreceptor survival and function. RPE65-catalyzed synthesis of 11-cis-retinol from all-trans-retinyl esters in the visual cycle is negatively regulated, through a heretofore unknown mechanism, by the fatty acid transport protein FATP4, mutations in which are associated with ichthyosis prematurity syndrome (IPS). Here, we analyzed the interaction between deletion mutants of FATP4 and RPE65 and the impacts of IPS-associated FATP4 mutations on RPE65 expression, 11-cis-retinol synthesis, and all-trans-retinyl ester synthesis. Our results suggest that the interaction between FATP4 and RPE65 contributes to the inhibition of RPE65 function and that IPS-associated nonsense and missense mutations in FATP4 have different effects on the visual cycle.

Indexed as

Gene Deletioncis-trans-IsomerasesCodon, NonsenseFatty Acid Transport ProteinsGene Expression RegulationHEK293 CellsHumansIchthyosisInfant, Premature, DiseasesPoint MutationRetinoid IsomerohydrolaseVitamin Acis-trans-IsomerasesCodon, NonsenseFatty Acid Transport ProteinsRetinoid IsomerohydrolaseSLC27A4 protein, humanVitamin Aacyl-CoA synthetaseichthyosis prematurity syndromeLeber congenital amaurosislecithin:retinol acyltransferaseretinal pigment epitheliumretinoid visual cycle

Identifiers

PMID31595490
PMCPMC7012757
OpenAlexW2980182251

What OpenQuestion holds

Textmetadata
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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.