Waters K M, Miller C W, Ntambi J M
Department of Biochemistry, University of Wisconsin, Madison 53706, USA.
Biochem Biophys Res Commun. 1997 Apr 28;233(3):838-43. doi: 10.1006/bbrc.1997.6550.
The effect of thyroid hormone on stearoyl-CoA desaturase gene 1 (SCD1) expression was investigated in mouse liver. Daily injections of 15 micrograms triiodothyronine (T3)/100 g body weight to hypothyroid mice resulted in repression of SCD1 mRNA levels by more than 50% in 48 hours and up to 65% in 6 days. Transient co-transfections were performed with an expression vector for T3 receptor alpha (T3R alpha) in HepG2 cells using chimeric reporter gene constructs of the SCD1 5'-flanking region. Transcriptional repression of the SCD1 putative promoter was observed upon treatment with 100 nM T3 when cotransfected with T3R alpha, but not without cotransfection of receptor. Transient gene expression studies localized a T3 response region to a 70-bp sequence in the SCD1 putative promoter. Eliminating the TATA box and an AP-2 binding site, DNA mobility shift analysis demonstrated specific binding of in vivo nuclear protein from mouse liver nuclear extract to a 43-bp sequence. DNA mobility shift with purified T3R alpha confirmed the presence of a T3 receptor binding site in this thyroid hormone-responsive region. These data indicate that SCD1 contains a negative T3 response region in its proximal promoter.
研究了甲状腺激素对小鼠肝脏中硬脂酰辅酶A去饱和酶基因1(SCD1)表达的影响。对甲状腺功能减退的小鼠每日注射15微克三碘甲状腺原氨酸(T3)/100克体重,48小时内SCD1 mRNA水平降低超过50%,6天内高达65%。在HepG2细胞中使用SCD1 5'侧翼区域的嵌合报告基因构建体与T3受体α(T3Rα)的表达载体进行瞬时共转染。当与T3Rα共转染时,用100 nM T3处理可观察到SCD1假定启动子的转录抑制,但未共转染受体时则未观察到。瞬时基因表达研究将T3反应区域定位到SCD1假定启动子中的一个70 bp序列。去除TATA盒和一个AP-2结合位点后,DNA迁移率变动分析表明,小鼠肝脏核提取物中的体内核蛋白与一个43 bp序列发生特异性结合。用纯化的T3Rα进行DNA迁移率变动分析证实了该甲状腺激素反应区域中存在T3受体结合位点。这些数据表明,SCD1在其近端启动子中含有一个负性T3反应区域。