Evidence map›Paper›PMID 23705025›Full record

ArticlePloS one2013

Identification of antithrombin-modulating genes. Role of LARGE, a gene encoding a bifunctional glycosyltransferase, in the secretion of proteins?

María Eugenia de la Morena-Barrio, Alfonso Buil, Ana Isabel Antón, Irene Martínez-Martínez, Antonia Miñano, Ricardo Gutiérrez-Gallego, José Navarro-Fernández, Sonia Aguila, Juan Carlos Souto, Vicente Vicente and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. 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
0.8field-weighted citation impact, top 26% 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, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Defects of splicing in antithrombin deficiency.Research and practice in thrombosis and haemostasis · 2017
    Article
  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

12 authors at 5 institutions in 1 country.

María Eugenia de la Morena-BarrioCentro Regional de Hemodonación, Servicio de Hematología y Oncología Médica, HU Morales Meseguer, Regional Campus of International Excellence Campus Mare Nostrum University of Murcia, Murcia, Spain.
Alfonso Buil
Ana Isabel Antón
Irene Martínez-Martínez
Antonia Miñano
Ricardo Gutiérrez-Gallego
José Navarro-Fernández
Sonia Aguila
Juan Carlos Souto
Vicente Vicente
José Manuel Soria
Javier Corral
Universidad de Murcia · ESCentro Regional de Hemodonación · ESHospital de Sant Pau · ESParc de Salut · ESSociedad Española de Trombosis y Hemostasia · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The haemostatic relevance of antithrombin together with the low genetic variability of SERPINC1, and the high heritability of plasma levels encourage the search for modulating genes. We used a hypothesis-free approach to identify these genes, evaluating associations between plasma antithrombin and 307,984 polymorphisms in the GAIT study (352 individuals from 21 Spanish families). Despite no SNP reaching the genome wide significance threshold, we verified milder positive associations in 307 blood donors from a different cohort. This validation study suggested LARGE, a gene encoding a protein with xylosyltransferase and glucuronyltransferase activities that forms heparin-like linear polysaccharides, as a potential modulator of antithrombin based on the significant association of one SNPs, rs762057, with anti-FXa activity, particularly after adjustment for age, sex and SERPINC1 rs2227589 genotype, all factors influencing antithrombin levels (p = 0.02). Additional results sustained this association. LARGE silencing inHepG2 and HEK-EBNA cells did not affect SERPINC1 mRNA levels but significantly reduced the secretion of antithrombin with moderate intracellular retention. Milder effects were observed on α1-antitrypsin, prothrombin and transferrin. Our study suggests LARGE as the first known modifier of plasma antithrombin, and proposes a new role for LARGE in modulating extracellular secretion of certain glycoproteins.

Indexed as

AdultAntithrombinsCase-Control StudiesFactor XaFemaleGene SilencingGenetic Association StudiesGenome-Wide Association StudyGlycomicsGlycoproteinsHaplotypesHEK293 CellsHep G2 CellsHumansMaleN-AcetylglucosaminyltransferasesAntithrombinsFactor XaGlycoproteinsLARGE1 protein, humanN-Acetylglucosaminyltransferases

Identifiers

PMID23705025
PMCPMC3660365
OpenAlexW2073610398

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.