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碳水化合物消化/吸收相关基因表达的调控。

Regulation of the expression of carbohydrate digestion/absorption-related genes.

作者信息

Goda T

机构信息

Laboratory of Nutritional Physiology, School of Food and Nutritional Sciences, University of Shizuoka, Japan.

出版信息

Br J Nutr. 2000 Dec;84 Suppl 2:S245-8. doi: 10.1079/096582197388626.

Abstract

To explore the underlying molecular mechanism whereby nutrients modulate the expression of intestinal digestion/absorption-related genes, we have cloned the 5' flanking regions of two representing disaccharidase genes, i.e. sucrase-isomaltase (SI) and lactase-phlorizin hydrolase (LPH), and investigated whether the binding activity of putative common nuclear factor(s) binding to the cis-elements located in these regions is altered by dietary manipulations. Oro-gastric feeding of a sucrose-containing diet to rats caused parallel increases in SI mRNA and LPH mRNA levels within 3 h. Among the monosaccharides tested, fructose gave rise to the most prominent increase in the mRNA levels of SI and LPH genes, which were accompanied by a coordinate rise in the mRNA levels of two microvillar hexose transporters, i.e. SGLT1 and GLUT5. Nuclear run-on assays revealed that fructose, but not glucose, increased the transcription of SI, LPH and GLUT5. DNase I footprinting analysis of the rat LPH gene showed that the protected region conserved the same sequence as the cis-element (CE-LPH1) reported in the pig LPH gene. Electrophoretic mobility shift assay using CE-LPH1 and the related cis-element of SI gene (SIF1) revealed that nuclear extracts from the jejunum of rats fed the high-starch diet gave greater density of retarded bands than those of rats fed the low-starch diet. Force feeding a fructose diet gave rise to an increase in the binding of the dimeric nuclear protein (Cdx-2) to the SIF1 element. These results suggest that the cis-elements of CE-LPH1 and SIF1 might be involved in the carbohydrate-induced increases of the transcription of LPH and SI, presumably through a change in the expression and/or binding activity of Cdx-2.

摘要

为了探究营养素调节肠道消化/吸收相关基因表达的潜在分子机制,我们克隆了两个代表性双糖酶基因,即蔗糖酶-异麦芽糖酶(SI)和乳糖酶-根皮苷水解酶(LPH)的5'侧翼区域,并研究了与这些区域中顺式元件结合的假定共同核因子的结合活性是否会因饮食操作而改变。给大鼠经口胃饲含蔗糖饮食在3小时内使SI mRNA和LPH mRNA水平平行升高。在所测试的单糖中,果糖使SI和LPH基因的mRNA水平升高最为显著,同时两个微绒毛己糖转运体,即SGLT1和GLUT5的mRNA水平也协同升高。核转录分析表明,果糖而非葡萄糖增加了SI,LPH和GLUT5的转录。大鼠LPH基因的DNase I足迹分析表明,受保护区域与猪LPH基因中报道的顺式元件(CE-LPH1)具有相同序列。使用CE-LPH1和SI基因相关顺式元件(SIF1)进行的电泳迁移率变动分析表明,高淀粉饮食喂养的大鼠空肠核提取物产生的阻滞带密度比低淀粉饮食喂养的大鼠更高。强制喂食果糖饮食导致二聚体核蛋白(Cdx-2)与SIF1元件的结合增加。这些结果表明,CE-LPH1和SIF1的顺式元件可能参与了碳水化合物诱导的LPH和SI转录增加,大概是通过Cdx-2表达和/或结合活性的改变。

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