학술논문

Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes
Document Type
article
Author
Rebecca KeenerSurya B. ChhetriCarla J. ConnellyMargaret A. TaubMatthew P. ConomosJoshua WeinstockBohan NiBenjamin StroberStella AslibekyanPaul L. AuerLucas BarwickLewis C. BeckerJohn BlangeroEugene R. BleeckerJennifer A. BrodyBrian E. CadeJuan C. CeledonYi-Cheng ChangL. Adrienne CupplesBrian CusterBarry I. FreedmanMark T. GladwinSusan R. HeckbertLifang HouMarguerite R. IrvinCarmen R. IsasiJill M. JohnsenEimear E. KennyCharles KooperbergRyan L. MinsterTake NaseriSatupa’itea VialiSergei NekhaiNathan PankratzPatricia A. PeyserKent D. TaylorMarilyn J. TelenBaojun WuLisa R. YanekIvana V. YangChristine AlbertDonna K. ArnettAllison E. Ashley-KochKathleen C. BarnesJoshua C. BisThomas W. BlackwellEric BoerwinkleEsteban G. BurchardApril P. CarsonZhanghua ChenYii-Der Ida ChenDawood DarbarMariza de AndradePatrick T. EllinorMyriam FornageBruce D. GelbFrank D. GillilandJiang HeTalat IslamStefan KaabSharon L. R. KardiaShannon KellyBarbara A. KonkleRajesh KumarRuth J. F. LoosFernando D. MartinezStephen T. McGarveyDeborah A. MeyersBraxton D. MitchellCourtney G. MontgomeryKari E. NorthNicholette D. PalmerJuan M. PeraltaBenjamin A. RabySusan RedlineStephen S. RichDan RodenJerome I. RotterIngo RuczinskiDavid SchwartzFrank SciurbaM. Benjamin ShoemakerEdwin K. SilvermanMoritz F. SinnerNicholas L. SmithAlbert V. SmithHemant K. TiwariRamachandran S. VasanScott T. WeissL. Keoki WilliamsYingze ZhangElad ZivLaura M. RaffieldAlexander P. ReinerNHLBI Trans-Omics for Precision Medicine (TOPMed) ConsortiumTOPMed Hematology and Hemostasis Working GroupTOPMed Structural Variation Working GroupMarios ArvanitisCarol W. GreiderRasika A. MathiasAlexis Battle
Source
Nature Communications, Vol 15, Iss 1, Pp 1-21 (2024)
Subject
Science
Language
English
ISSN
2041-1723
Abstract
Abstract 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.