Evidence map›Paper›PMID 18596935›Full record

ArticlePloS one2008

Targeted disruption of the PME-1 gene causes loss of demethylated PP2A and perinatal lethality in mice.

Silvia Ortega-Gutiérrez, Donmienne Leung, Scott Ficarro, Eric C Peters, Benjamin F Cravatt

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

24 citing papers in PubMed, 48 citations in OpenAlex.

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  7. Therapeutic targeting of PP2A.The international journal of biochemistry & cell biology · 2018
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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

5 authors at 2 institutions in 1 country.

Silvia Ortega-GutiérrezThe Skaggs Institute for Chemical Biology and Department of Cell Biology, The Scripps Research Institute, La Jolla, California, United States of America.
Donmienne Leung
Scott Ficarro
Eric C Peters
Benjamin F Cravatt
Scripps Research Institute · USGenomics Institute of the Novartis Research Foundation · US

Funding

Enzymes That Regulate Fatty Acid Amide Function In VivoR01DA015197 · NIDA · SCRIPPS RESEARCH INSTITUTE, THE · PI CRAVATT, BENJAMIN F · 2002 to 2009
$2.5M
NIDA NIH HHS DA015197NIDA NIH HHS R01 DA015197
6 · The paper itself

Abstract

backgroundPhosphoprotein phosphatase 2A (PP2A), a major serine-threonine protein phosphatase in eukaryotes, is an oligomeric protein comprised of structural (A) and catalytic (C) subunits to which a variable regulatory subunit (B) can associate. The C subunit contains a methyl ester post-translational modification on its C-terminal leucine residue, which is removed by a specific methylesterase (PME-1). Methylesterification is thought to control the binding of different B subunits to AC dimers, but little is known about its physiological significance in vivo. METHODOLOGY/PRINCIPAL

findingsHere, we show that targeted disruption of the PME-1 gene causes perinatal lethality in mice, a phenotype that correlates with a virtually complete loss of the demethylated form of PP2A in the nervous system and peripheral tissues. Interestingly, PP2A catalytic activity over a peptide substrate was dramatically reduced in PME-1(-/-) tissues, which also displayed alterations in phosphoproteome content.

conclusionsThese findings suggest a role for the demethylated form of PP2A in maintenance of enzyme function and phosphorylation networks in vivo.

Indexed as

AnimalsCarboxylic Ester HydrolasesCatalytic DomainGenes, LethalGene TargetingMethylationMiceMice, TransgenicModels, GeneticProtein Phosphatase 2Carboxylic Ester HydrolasesProtein Phosphatase 2protein phosphatase methylesterase-1

Identifiers

PMID18596935
PMCPMC2438471
OpenAlexW2011159058

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.