Department of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
Drug Metab Pharmacokinet. 2012;27(4):456-64. doi: 10.2133/dmpk.dmpk-11-sh-104. Epub 2012 Jan 13.
MCT4 (SLC16A3) is the third member of the monocarboxylate transporter (MCT) family and is involved in the transportation of metabolically important monocarboxylates such as lactate, pyruvate, acetate and ketone bodies. This study aimed to identify genetic variations of the SLC16A3 gene that may be present in the ethnic Chinese (n = 95) and Indian (n = 96) groups of the Singaporean population. The genetic variations in the promoter, coding region and exon-intron junctions of the SLC16A3 gene encoding the MCT4 transporter were screened by DNA sequencing. A total of 46 genetic variants were detected in the SLC16A3 gene, of which 33 are novel. Of these variants, 22 are located in the promoter regions, 2 in the 5' untranslated region (UTR), 10 in the coding exons (5 nonsynonymous and 5 synonymous variations), 6 in 3'UTR and 6 in the intron. Of the 5 nonsynonymous variants, only 44C>T (Ala15Val) was predicted by PolyPhen and SIFT as having a potentially damaging effect on protein function, whereas 55G>A (Gly19Ser), 574G>A (Val192Met) and 916G>A (Gly306Ser) had conflicting results between the SIFT and PolyPhen algorithms. Finally, 641C>T (Ser214Phe) was predicted to be a tolerated variant.
MCT4(SLC16A3)是单羧酸转运蛋白(MCT)家族的第三个成员,参与代谢重要的单羧酸如乳酸盐、丙酮酸、醋酸盐和酮体的转运。本研究旨在鉴定可能存在于新加坡华人(n=95)和印度人(n=96)群体中的 SLC16A3 基因的遗传变异。通过 DNA 测序筛选了编码 MCT4 转运蛋白的 SLC16A3 基因的启动子、编码区和外显子-内含子接头的遗传变异。在 SLC16A3 基因中共检测到 46 种遗传变异,其中 33 种是新的。这些变异中,22 种位于启动子区域,2 种位于 5'非翻译区(UTR),10 种位于编码外显子(5 种非同义变异和 5 种同义变异),6 种位于 3'UTR,6 种位于内含子。在 5 种非同义变异中,只有 44C>T(Ala15Val)被 PolyPhen 和 SIFT 预测为对蛋白质功能具有潜在破坏性影响,而 55G>A(Gly19Ser)、574G>A(Val192Met)和 916G>A(Gly306Ser)在 SIFT 和 PolyPhen 算法之间存在冲突结果。最后,641C>T(Ser214Phe)被预测为耐受变异。