Evidence map›Paper›PMID 40512334›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2025

Genomic Locus Tagged by Lung Function GWAS SNV rs12477314 (2q37.3) Acts as a Regulatory Region for a Systemic Inflammatory Phenotype.

Godwin M Grech, Katherine A Fawcett, Robert J Hall, Godfrey Grech, Roger Ellul-Micallef, Ian P Hall, Anthony G Fenech

Erratum issuedAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Godwin M GrechDepartment of Clinical Pharmacology and Therapeutics, Faculty of Medicine & Surgery, University of Malta, Msida, Malta.ORCID https://orcid.org/0009-0005-3251-2208
Katherine A FawcettDepartment of Population Health Sciences, University of Leicester, Leicester, UK.
Robert J HallDivision of Respiratory Medicine and NIHR Nottingham Biomedical Research Centre, University of Nottingham, Nottingham, UK.ORCID https://orcid.org/0000-0001-9114-7144
Godfrey GrechDepartment of Pathology, Faculty of Medicine & Surgery, University of Malta, Msida, Malta.
Roger Ellul-MicallefDepartment of Clinical Pharmacology and Therapeutics, Faculty of Medicine & Surgery, University of Malta, Msida, Malta.
Ian P HallDivision of Respiratory Medicine and NIHR Nottingham Biomedical Research Centre, University of Nottingham, Nottingham, UK.
Anthony G FenechDepartment of Clinical Pharmacology and Therapeutics, Faculty of Medicine & Surgery, University of Malta, Msida, Malta.

Funding

Malta Government Scholarship Scheme (MGSS)Wellcome Trust 225221Wellcome Trust Discovery Award
6 · The paper itself

Abstract

SNV rs12477314 (C>T; 1000G MAF = 0.14), which maps to an intergenic region on 2q37.3, is a genome-wide significant association signal for pulmonary function in genome-wide association study meta-analyses. Bioinformatic analysis revealed that the intergenic region in proximity to the sentinel SNV is enriched for histone methylation markers suggestive of active enhancer regions modifiable by DNA methylation. The aim of this study was to investigate the functionality of putative enhancer/s and their potential interaction with CpG islands in the genomic region tagged by rs12477314 and their relevance to lung disease, in particular COPD. Two independent CRISPR/Cas9n-targeted deletions of the putative enhancer/s were performed in an airway epithelial cell line (NCI-H460). Deletion clones were subjected to RNA-Seq, and differential expression gene (DEG) datasets were generated using the Cufflinks version 2.2.1 pipeline (p-FDR < 0.05). Biological pathway analysis was performed using Qiagen's Ingenuity Pathway Analysis. Associations with the blood proteome were explored in UK Biobank. Our results suggest that the deleted regions are co-acting enhancers regulating overlapping gene expression patterns. The DEG datasets from the two genomic deletions are enriched for similar canonical pathways, which may contribute to a pro-inflammatory phenotype. Pathway-based regulatory effects analysis of the two DEG datasets resulted in identifying potential downstream biological processes. There was overlap between the pathways identified in protein association datasets and the DEG datasets. Our results suggest that the genomic region tagged by SNV rs12477314 constitutes a regulatory region responsible for regulating biological pathways conducive to a systemic inflammatory phenotype.

Indexed as

Genome-Wide Association StudyInflammationLungPolymorphism, Single NucleotidePulmonary Disease, Chronic ObstructiveCpG IslandsDNA MethylationEnhancer Elements, GeneticHumansPhenotypebiological pathway analysisCOPDCRISPRDNA methylationenhancersRNA‐seqSNV

Identifiers

PMID40512334
PMCPMC12164972

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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.