Pregled bibliografske jedinice broj: 1238183
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids // American journal of human genetics, 109 (2022), 8; 1366-1387 doi:10.1016/j.ajhg.2022.06.012 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1238183 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
A multi-layer functional genomic analysis to
understand noncoding genetic variation in lipids
Autori
Ramdas, Shweta ; Judd, Jonathan ; Graham, Sarah E. ; Kanoni, Stavroula ; Wang, Yuxuan ; Surakka, Ida ; ... ; Kolčić, Ivana ; … ; Polašek, Ozren ; [et al.]
Kolaboracija
Million Vet Program ; Global Lipids Genetics Consortium
Izvornik
American journal of human genetics (0002-9297) 109
(2022), 8;
1366-1387
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
INTEGRATIVE ANALYSIS ; WIDE ASSOCIATION ; 3D GENOME ; VARIANTS ; CHOLESTEROL ; ANNOTATION ; OBESITY ; COMMON ; LOCI ; EXPRESSION
Sažetak
A major challenge of genome-wide association studies (GWASs) is to translate phenotypic associations into biological insights. Here, we integrate a large GWAS on blood lipids involving 1.6 million individuals from five ancestries with a wide array of functional genomic datasets to discover regulatory mechanisms underlying lipid associations. We first prioritize lipid-associated genes with expression quantitative trait locus (eQTL) colocalizations and then add chromatin interaction data to narrow the search for functional genes. Polygenic enrichment analysis across 697 annotations from a host of tissues and cell types confirms the central role of the liver in lipid levels and highlights the selective enrichment of adipose-specific chromatin marks in high-density lipoprotein cholesterol and triglycerides. Overlapping transcription factor (TF) binding sites with lipid-associated loci identifies TFs relevant in lipid biology. In addition, we present an integrative framework to prioritize causal variants at GWAS loci, producing a comprehensive list of candidate causal genes and variants with multiple layers of functional evidence. We highlight two of the prioritized genes, CREBRF and RRBP1, which show convergent evidence across functional datasets supporting their roles in lipid biology.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Ustanove:
Medicinski fakultet, Split
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE
- Nature Index