Novel mutations in scavenger receptor BI associated with high HDL cholesterol in humans

被引:67
作者
Brunham, L. R. [1 ]
Tietjen, I. [2 ]
Bochem, A. E. [3 ]
Singaraja, R. R. [1 ,2 ]
Franchini, P. L. [2 ]
Radomski, C. [2 ]
Mattice, M. [2 ]
Legendre, A. [2 ]
Hovingh, G. K. [3 ]
Kastelein, J. J. P. [3 ]
Hayden, M. R. [1 ]
机构
[1] Univ British Columbia, Child & Family Res Inst, Ctr Mol Med & Therapeut, Dept Med & Med Genet, Vancouver, BC V5Z 1M9, Canada
[2] Xenon Pharmaceut, Burnaby, BC, Canada
[3] Univ Amsterdam, Acad Med Ctr, Dept Vasc Med, NL-1105 AZ Amsterdam, Netherlands
关键词
atherosclerosis; HDL; lipids; lipoproteins; SR-BI; DENSITY-LIPOPROTEIN RECEPTOR; SR-BI; PLASMA HDL; I GENE; TARGETED MUTATION; TANGIER-DISEASE; ABCA1; ATHEROSCLEROSIS; POPULATION; DEFICIENCY;
D O I
10.1111/j.1399-0004.2011.01682.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The scavenger receptor class B, member 1 (SR-BI), is a key cellular receptor for high-density lipoprotein (HDL) in mice, but its relevance to human physiology has not been well established. Recently a family was reported with a mutation in the gene encoding SR-BI and high HDL cholesterol (HDL-C). Here we report two additional individuals with extremely high HDL-C (greater than the 90th percentile for age and gender) with rare mutations in the gene encoding SR-BI. These mutations segregate with high HDL-C in family members of each proband and are associated with a 37% increase in plasma HDL-C in heterozygous individuals carrying them. Both mutations occur at highly conserved positions in the large extracellular loop region of SR-BI and are predicted to impair the function of the SR-BI protein. Our findings, combined with the prior report of a single mutation in the gene encoding SR-BI, further validate that mutations in SR-BI are a rare but recurring cause of elevated HDL-C in humans.
引用
收藏
页码:575 / 581
页数:7
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