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一个在雄性转基因大鼠中优先驱动基因表达的启动子。

A promoter that drives gene expression preferentially in male transgenic rats.

机构信息

Department of Obstetrics and Gynecology, First Affiliated Hospital, Xi'an Jiaotong University, Xi'an, Shaanxi, China.

出版信息

Transgenic Res. 2014 Apr;23(2):341-9. doi: 10.1007/s11248-013-9773-9. Epub 2013 Dec 15.

Abstract

Gender-preferential gene expression is a widespread phenomenon in humans. It is important to study how gender differences influence the pathogenesis of various diseases and response to specific drugs. The aim of this study is to determine if the mouse albumin enhancer/promoter may serve as the promoter to introduce gender-preferential gene expression in transgenic animals. We created four independent transgenic rat lines in which the human C-reactive protein transgene was under the control of mouse albumin enhancer/promoter. Quantitative real time RT-PCR analysis showed that transgene expression in the liver of male rats was significantly higher than transgene expression in the female rats (P < 0.05).There was a 5.3-fold (male/female) difference in line-519, and a 12.2-fold (male/female) difference in line-488. Enzyme-linked immunosorbent assay showed that the serum of male transgenic rats had a 13- to 679-fold difference at the protein level on transgene production compared with female transgenic rats. The male-to-female difference in gene expression was 10- to 17-fold in the liver of transgenic rats. Orchiectomy dramatically reduced protein production from the transgene in the liver. Testosterone administration into female rats did not increase the transgene expression, but estrogen administration into the male rats reduced transgene expression. This study provides a valuable tool for investigating the pathological roles of genes that are expressed in a gender-preferential manner in human disease.

摘要

性别偏好基因表达是人类中普遍存在的现象。研究性别差异如何影响各种疾病的发病机制和对特定药物的反应非常重要。本研究旨在确定小鼠白蛋白增强子/启动子是否可作为引入转基因动物中性别偏好基因表达的启动子。我们创建了四条独立的转基因大鼠品系,其中人类 C 反应蛋白转基因受小鼠白蛋白增强子/启动子的控制。定量实时 RT-PCR 分析表明,雄性大鼠肝脏中转基因的表达明显高于雌性大鼠(P < 0.05)。在 519 号线中存在 5.3 倍(雄性/雌性)的差异,在 488 号线中存在 12.2 倍(雄性/雌性)的差异。酶联免疫吸附测定显示,雄性转基因大鼠的血清中转基因产物的蛋白水平比雌性转基因大鼠高 13-679 倍。在转基因大鼠的肝脏中,基因表达的雄性与雌性差异为 10-17 倍。去势术可显著降低肝脏中转基因的蛋白产生。向雌性大鼠中给予睾酮不会增加转基因的表达,但向雄性大鼠中给予雌激素会降低转基因的表达。本研究为研究在人类疾病中以性别偏好方式表达的基因的病理作用提供了有价值的工具。

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