THOC5 : A novel gene involved in HDL-cholesterol metabolism
(2013) In Journal of Lipid Research 54(11). p.3170-3176- Abstract
Although numerous genes are known to regulate serum lipid traits, identified variants explain only a small proportion of the expected heritability. We intended to identify further genetic variants associated with lipid phenotypes in a self-contained population of Sorbs in Germany. We performed a genome-wide association study (GWAS) on LDL-cholesterol, HDL-cholesterol (HDL-C), and triglyceride (TG) levels in 839 Sorbs. All single-nucleotide polymorphisms with a P value <0.01 were subjected to a meta-analysis, including an independent Swedish cohort (Diabetes Genetics Initiative; n = ∼ 3,100). Novel association signals with the strongest effects were subjected to replication studies in an additional German cohort (Berlin, n = 2,031).... (More)
Although numerous genes are known to regulate serum lipid traits, identified variants explain only a small proportion of the expected heritability. We intended to identify further genetic variants associated with lipid phenotypes in a self-contained population of Sorbs in Germany. We performed a genome-wide association study (GWAS) on LDL-cholesterol, HDL-cholesterol (HDL-C), and triglyceride (TG) levels in 839 Sorbs. All single-nucleotide polymorphisms with a P value <0.01 were subjected to a meta-analysis, including an independent Swedish cohort (Diabetes Genetics Initiative; n = ∼ 3,100). Novel association signals with the strongest effects were subjected to replication studies in an additional German cohort (Berlin, n = 2,031). In the initial GWAS in the Sorbs, we identified 14 loci associated with lipid phenotypes reaching P values <10 -5 and confirmed significant effects for 18 previously reported loci. The combined meta-analysis of the three study cohorts (n(HDL) = 6041; n (LDL) = 5,995; n(TG) = 6,087) revealed a novel association for a variant in THOC5 (rs8135828) with serum HDL-C levels (P = 1.78 × 10-7; Z -score = -5.221). Consistently, the variant was also associated with circulating APOA1 levels in Sorbs. The small interfering RNA-mediated mRNA silencing of THOC5 in HepG2 cells resulted in lower mRNA levels of APOA1, SCARB1, and ABCG8 (all P < 0.05). We propose THOC5 to be a novel gene involved in the regulation of serum HDL-C levels.
(Less)
- author
- organization
- publishing date
- 2013-11-01
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- Genomewide-association study, MRNA silencing, Single nucleotide polymorphism
- in
- Journal of Lipid Research
- volume
- 54
- issue
- 11
- pages
- 7 pages
- publisher
- American Society for Biochemistry and Molecular Biology
- external identifiers
-
- scopus:84885996384
- pmid:24023261
- ISSN
- 0022-2275
- DOI
- 10.1194/jlr.M039420
- language
- English
- LU publication?
- yes
- id
- 5b4c6ec6-7f84-4819-8057-8aa28014d493
- date added to LUP
- 2018-10-01 13:52:31
- date last changed
- 2024-12-24 15:01:51
@article{5b4c6ec6-7f84-4819-8057-8aa28014d493, abstract = {{<p>Although numerous genes are known to regulate serum lipid traits, identified variants explain only a small proportion of the expected heritability. We intended to identify further genetic variants associated with lipid phenotypes in a self-contained population of Sorbs in Germany. We performed a genome-wide association study (GWAS) on LDL-cholesterol, HDL-cholesterol (HDL-C), and triglyceride (TG) levels in 839 Sorbs. All single-nucleotide polymorphisms with a P value <0.01 were subjected to a meta-analysis, including an independent Swedish cohort (Diabetes Genetics Initiative; n = ∼ 3,100). Novel association signals with the strongest effects were subjected to replication studies in an additional German cohort (Berlin, n = 2,031). In the initial GWAS in the Sorbs, we identified 14 loci associated with lipid phenotypes reaching P values <10 <sup>-5</sup> and confirmed significant effects for 18 previously reported loci. The combined meta-analysis of the three study cohorts (n<sub>(HDL)</sub> = 6041; n <sub>(LDL)</sub> = 5,995; n<sub>(TG)</sub> = 6,087) revealed a novel association for a variant in THOC5 (rs8135828) with serum HDL-C levels (P = 1.78 × 10<sup>-7</sup>; Z -score = -5.221). Consistently, the variant was also associated with circulating APOA1 levels in Sorbs. The small interfering RNA-mediated mRNA silencing of THOC5 in HepG2 cells resulted in lower mRNA levels of APOA1, SCARB1, and ABCG8 (all P < 0.05). We propose THOC5 to be a novel gene involved in the regulation of serum HDL-C levels.</p>}}, author = {{Keller, Maria and Schleinitz, Dorit and Förster, Julia and Tönjes, Anke and Böttcher, Yvonne and Fischer-Rosinsky, Antje and Breitfeld, Jana and Weidle, Kerstin and Rayner, Nigel W. and Burkhardt, Ralph and Enigk, Beate and Müller, Ines and Halbritter, Jan and Koriath, Moritz and Pfeiffer, Andreas and Krohn, Knut and Groop, Leif and Spranger, Joachim and Stumvoll, Michael and Kovacs, Peter}}, issn = {{0022-2275}}, keywords = {{Genomewide-association study; MRNA silencing; Single nucleotide polymorphism}}, language = {{eng}}, month = {{11}}, number = {{11}}, pages = {{3170--3176}}, publisher = {{American Society for Biochemistry and Molecular Biology}}, series = {{Journal of Lipid Research}}, title = {{THOC5 : A novel gene involved in HDL-cholesterol metabolism}}, url = {{http://dx.doi.org/10.1194/jlr.M039420}}, doi = {{10.1194/jlr.M039420}}, volume = {{54}}, year = {{2013}}, }