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Accès ouvert déclaré 2024 article

Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes

8Citations signalées, ce qui n’est pas une note de qualité
62Institutions déclarées
4Pays d’affiliation déclarés

Rattachement africain : us, tw, ws, de. Niveau de preuve : code pays fourni par la source.

Le résumé fourni par la source

Genome-wide association studies (GWAS) have become well-powered to detect loci associated with telomere length. However, no prior work has validated genes nominated by GWAS to examine their role in telomere length regulation. We conducted a multi-ancestry meta-analysis of 211,369 individuals and identified five novel association signals. Enrichment analyses of chromatin state and cell-type heritability suggested that blood/immune cells are the most relevant cell type to examine telomere length association signals. We validated specific GWAS associations by overexpressing KBTBD6 or POP5 and demonstrated that both lengthened telomeres. CRISPR/Cas9 deletion of the predicted causal regions in K562 blood cells reduced expression of these genes, demonstrating that these loci are related to transcriptional regulation of KBTBD6 and POP5. Our results demonstrate the utility of telomere length GWAS in the identification of telomere length regulation mechanisms and validate KBTBD6 and POP5 as genes affecting telomere length regulation.

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Le contrôle bibliographique ouvert

DOI retrouvé dans Crossref DOI retrouvé ; titre concordant.

Titre Crossref
Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes
Date Crossref
24/05/2024
Éditeur
Springer Science and Business Media LLC
Type
journal-article

Ce recoupement confirme des métadonnées liées au DOI. Il ne confirme ni la méthode ni les conclusions de l’étude, et il ne compte pas comme une seconde source scientifique indépendante.

Les institutions déclarées

Johns Hopkins UniversityUniversity of WashingtonHarvard UniversityUniversity of Alabama at BirminghamMedical College of WisconsinEmmes (United States)Johns Hopkins MedicineThe University of Texas Rio Grande ValleyUniversity of ArizonaBrigham and Women's HospitalUniversity of PittsburghNational Taiwan UniversityInstitute of Biomedical Sciences, Academia SinicaBoston UniversityNational Heart, Lung, and Blood InstituteFramingham Heart StudyUniversity of California, San FranciscoPacific Research InstituteVitalantVitalant Research InstituteWake Forest UniversityUniversity of Maryland, BaltimoreNorthwestern UniversityAlbert Einstein College of MedicineGenomic Health (United States)Icahn School of Medicine at Mount SinaiFred Hutch Cancer CenterNational University of SamoaBrown UniversityYale UniversityHoward UniversityUniversity of MinnesotaUniversity of MichiganUCLA Medical CenterHarbor–UCLA Medical CenterDuke Medical CenterHenry Ford HealthUniversity of Colorado BoulderUniversity of South CarolinaUniversity of Colorado AnschutzUniversity of Colorado DenverThe University of Texas Health Science Center at HoustonJackson Memorial HospitalUniversity of Mississippi Medical CenterUniversity of Southern CaliforniaUniversity of Illinois ChicagoMayo ClinicBroad InstituteChild Health and Development InstitutePediatrics and GeneticsTulane UniversityLMU KlinikumLudwig-Maximilians-Universität MünchenUCSF Benioff Children's HospitalLurie Children's HospitalOklahoma Medical Research FoundationUniversity of North Carolina at Chapel HillBoston Children's HospitalUniversity of VirginiaVanderbilt UniversityVanderbilt University Medical CenterUniversity of California, Santa Cruz

Une affiliation ne permet pas de déduire la nationalité d’un auteur.

Les sujets associés

Telomeres, Telomerase, and SenescenceGenomics and Chromatin DynamicsEpigenetics and DNA Methylation

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