Thymidylate synthase: a novel genetic determinant of plasma homocysteine and folate levels

被引:113
作者
Trinh, BN
Ong, CN
Coetzee, GA
Yu, MC
Laird, PW [1 ]
机构
[1] Univ So Calif, Keck Sch Med, Dept Surg, Norris Comprehens Canc Ctr, Los Angeles, CA 90089 USA
[2] Univ So Calif, Keck Sch Med, Dept Biochem, Norris Comprehens Canc Ctr, Los Angeles, CA 90089 USA
[3] Univ So Calif, Keck Sch Med, Dept Biol Mol, Norris Comprehens Canc Ctr, Los Angeles, CA 90089 USA
[4] Univ So Calif, Keck Sch Med, Norris Comprehens Canc Ctr, Dept Urol, Los Angeles, CA USA
[5] Univ So Calif, Norris Comprehens Canc Ctr, Keck Sch Med, Dept Prevent Med, Los Angeles, CA USA
[6] Natl Univ Singapore, Dept Community Occupat & Family Med, Singapore, Singapore
关键词
D O I
10.1007/s00439-002-0779-2
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The thymidylate synthase gene (TYMS or TS) encodes a tightly regulated enzyme that catalyzes the conversion of deoxyuridylate to thymidylate, and contains a tandem repeat polymorphism that affects expression of the enzyme. We have investigated the relationship between TYMS genotype and plasma concentrations of homocysteine and folate in a cohort of 505 Chinese from Singapore. TYMS 313 genotype was associated with reduced plasma folate and, among individuals with low dietary folate intake, with elevated plasma homocysteine levels. These associations were independent of the well-established methylenetetrahydrofolate reductase (MTHFR) C677T genotype effects on plasma folate and homocysteine levels. Our results suggest that TYMS and MTHFR compete for limiting supplies of folate required for the remethylation of homocysteine. These genetic determinants of plasma folate and homocysteine levels may be useful in identifying individuals at increased risk for cardiovascular disease.
引用
收藏
页码:299 / 302
页数:4
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