Lipoprotein lipase gene polymorphism rs1059611 functionally influences serum lipid concentrations

被引:11
作者
Mo, Xingbo [1 ,2 ]
Liu, Xuehui [1 ,2 ]
Wang, Laiyuan [1 ,2 ]
Li, Hongfan [1 ,2 ]
Lu, Xiangfeng [1 ,2 ]
Huang, Jianfeng [1 ,2 ]
Chen, Jichun [1 ,2 ]
Cao, Jie [1 ,2 ]
Li, Jianxin [1 ,2 ]
Chen, Shufeng [1 ,2 ]
Tang, Yida [2 ,3 ]
Peng, Xiaozhong [4 ,5 ]
Gu, Dongfeng [1 ,2 ]
机构
[1] Chinese Acad Med Sci, State Key Lab Cardiovasc Dis, Natl Ctr Cardiovasc Dis, Div Populat Genet,Fuwai Hosp, Beijing 100037, Peoples R China
[2] Peking Union Med Coll, Beijing 100037, Peoples R China
[3] Chinese Acad Med Sci, State Key Lab Cardiovasc Dis, Natl Ctr Cardiovasc Dis, Dept Cardiol,Fuwai Hosp, Beijing 100037, Peoples R China
[4] Chinese Acad Med Sci, State Key Lab Med Mol Biol, Inst Basic Med Sci, Beijing 100005, Peoples R China
[5] Peking Union Med Coll, Beijing 100005, Peoples R China
基金
中国国家自然科学基金;
关键词
Lipid; Lipoprotein lipase; Expression; Transcription factor; HIGH-DENSITY-LIPOPROTEIN; HAPLOTYPE STRUCTURE; HEART-DISEASE; TRIGLYCERIDES; ASSOCIATION; CHOLESTEROL; PREVALENCE; DEFICIENCY; METABOLISM; VARIANTS;
D O I
10.1016/j.atherosclerosis.2013.05.005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Dozens of single nucleotide polymorphisms (SNPs) in the lipoprotein lipase (LPL) gene have been reported to be associated with lipid concentrations. The aim of this study was to validate the association between rs1059611 in the LPL gene and serum lipid concentrations in the Chinese Han population and explore the biological relevance. Methods: A total of 5664 participants were recruited and genotyped for the SNP. Gene expression levels of LPL in blood cells were evaluated by real-time PCR and western blotting analysis. The functional potential of the SNP was examined by luciferase reporter assay and electrophoretic mobility-shift assay (EMSA). Results: We observed significant associations between rs1059611 and increased HDL-C (P = 5.65 x 10(-5)) and decreased TG concentrations (P = 2.68 x 10(-7)). We also found that participants with the C allele had higher mRNA expression level (P = 0.0334) and protein expression level (P = 0.0641) of LPL. The luciferase activity of the rs1059611 T construct was 0.69-fold of the rs1059611 C construct (P = 0.0009). The EMSA showed that the binding of the transcription factor(s) differed for the alleles of the SNP. Conclusion: The results of our study demonstrated that rs1059611 was associated with HDL-C and TG concentrations in Chinese Han population and might have a functional effect on the transcription of LPL by differential binding of transcription factors. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:511 / 516
页数:6
相关论文
共 22 条
  • [1] A systematic analysis of disease-associated variants in the 3′ regulatory regions of human protein-coding genes II:: the importance of mRNA secondary structure in assessing the functionality of 3′ UTR variants
    Chen, Jian-Min
    Ferec, Claude
    Cooper, David N.
    [J]. HUMAN GENETICS, 2006, 120 (03) : 301 - 333
  • [2] Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase
    Clark, AG
    Weiss, KM
    Nickerson, DA
    Taylor, SL
    Buchanan, A
    Stengård, J
    Salomaa, V
    Vartiainen, E
    Perola, M
    Boerwinkle, E
    Sing, CF
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (02) : 595 - 612
  • [3] Genetic variations at the lipoprotein lipase gene influence plasma lipid concentrations and interact with plasma n-6 polyunsaturated fatty acids to modulate lipid metabolism
    Garcia-Rios, Antonio
    Delgado-Lista, Javier
    Perez-Martinez, Pablo
    Phillips, Catherine M.
    Ferguson, Jane F.
    Gjelstad, Ingrid M. F.
    Williams, Christine M.
    Karlstrom, Brita
    Kiec-Wilkh, Beata
    Blaak, Ellen E.
    Lairon, Denis
    Planells, Richard
    Malczewska-Malec, Malgorzata
    Defoort, Catherine
    Riserus, Ulf
    Saris, Wim H. M.
    Lovegrove, Julie A.
    Drevon, Christian A.
    Roche, Helen M.
    Lopez-Miranda, Jose
    [J]. ATHEROSCLEROSIS, 2011, 218 (02) : 416 - 422
  • [4] Gaudet D, 2012, GENE THER, V19, P1
  • [5] Gene therapy for lipoprotein lipase deficiency
    Gaudet, Daniel
    Methot, Julie
    Kastelein, John
    [J]. CURRENT OPINION IN LIPIDOLOGY, 2012, 23 (04) : 310 - 320
  • [6] Goldberg IJ, 1996, J LIPID RES, V37, P693
  • [7] The 3′ untranslated region of the lipoprotein lipase gene:: Haplotype structure and association with post-heparin plasma lipase activity
    Goodarzi, MO
    Wong, H
    Quiñones, MJ
    Taylor, KD
    Guo, XQ
    Castellani, LW
    Antoine, HJ
    Yang, HY
    Hsueh, WA
    Rotter, JI
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2005, 90 (08) : 4816 - 4823
  • [8] Prevalence of the metabolic syndrome and overweight among adults in China
    Gu, DF
    Reynolds, K
    Wu, XG
    Chen, F
    Duan, XF
    Reynolds, RF
    Whelton, PK
    He, J
    [J]. LANCET, 2005, 365 (9468) : 1398 - 1405
  • [9] GENETIC AND ENVIRONMENTAL-INFLUENCES ON SERUM-LIPID LEVELS IN TWINS
    HELLER, DA
    DEFAIRE, U
    PEDERSEN, NL
    DAHLEN, G
    MCCLEARN, GE
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1993, 328 (16) : 1150 - 1156
  • [10] Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans
    Kathiresan, Sekar
    Melander, Olle
    Guiducci, Candace
    Surti, Aarti
    Burtt, Noel P.
    Rieder, Mark J.
    Cooper, Gregory M.
    Roos, Charlotta
    Voight, Benjamin F.
    Havulinna, Aki S.
    Wahlstrand, Bjorn
    Hedner, Thomas
    Corella, Dolores
    Tai, E. Shyong
    Ordovas, Jose M.
    Berglund, Goran
    Vartiainen, Erkki
    Jousilahti, Pekka
    Hedblad, Bo
    Taskinen, Marja-Riitta
    Newton-Cheh, Christopher
    Salomaa, Veikko
    Peltonen, Leena
    Groop, Leif
    Altshuler, David M.
    Orho-Melander, Marju
    [J]. NATURE GENETICS, 2008, 40 (02) : 189 - 197