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转基因小鼠中大鼠心房利钠因子基因调控序列的顺式显性

cis-dominance of rat atrial natriuretic factor gene regulatory sequences in transgenic mice.

作者信息

Seidman C E, Schmidt E V, Seidman J G

机构信息

Division of Cardiology, Brigham and Women's Hospital, Boston, MA 02115.

出版信息

Can J Physiol Pharmacol. 1991 Oct;69(10):1486-92. doi: 10.1139/y91-223.

Abstract

We have produced transgenic mice that express the prokaryotic marker protein chloramphenicol acetyltransferase under the control of regulatory sequences derived from the rat atrial natriuretic factor gene. The transgene, which contains 2.4 kilobases of the rat atrial natriuretic factor gene regulatory region, was found to direct 4000-fold more chloramphenicol acetyltransferase expression in adult atria than in ventricles. Low-level activity was also detected in the hypothalamus, demonstrating that these sequences contain the signals necessary for cardiac and central nervous system expression of the hormone atrial natriuretic factor. Developmental analyses showed early, high-level transgene expression in fetal atrial and ventricular tissues but marked reduction of ventricular transgene expression following birth. Further, the developmental expression patterns of the endogenous murine atrial natriuretic factor gene and rat transgene were found to be quite distinct. Although both the rat and mouse atrial natriuretic factor genes are activated early in embryogenesis, perinatal ventricular expression appears to differ in these two rodent species. The transgene is expressed in a pattern analogous to the neonatal rat rather than the endogenous murine gene. These studies demonstrate that the cis-acting signals required for correct tissue specificity and developmental regulation of the rat atrial natriuretic factor gene are encoded in this 2.4-kilobase fragment and that these sequences act in a dominant fashion.

摘要

我们培育出了转基因小鼠,这些小鼠在源自大鼠心钠素基因的调控序列控制下表达原核标记蛋白氯霉素乙酰转移酶。该转基因包含2.4千碱基的大鼠心钠素基因调控区,发现在成年心房中指导的氯霉素乙酰转移酶表达比心室中高4000倍。在下丘脑中也检测到低水平活性,表明这些序列包含心钠素在心脏和中枢神经系统表达所需的信号。发育分析显示,转基因在胎儿心房和心室组织中早期高水平表达,但出生后心室转基因表达显著降低。此外,发现内源性小鼠心钠素基因和大鼠转基因的发育表达模式截然不同。虽然大鼠和小鼠的心钠素基因在胚胎发育早期都被激活,但围产期心室表达在这两种啮齿动物中似乎有所不同。转基因以类似于新生大鼠而非内源性小鼠基因的模式表达。这些研究表明,大鼠心钠素基因正确的组织特异性和发育调控所需的顺式作用信号编码在这个2.4千碱基的片段中,并且这些序列以显性方式起作用。

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