Alcorn J L, Hammer R E, Graves K R, Smith M E, Maika S D, Michael L F, Gao E, Wang Y, Mendelson C R
Department of Biochemistry, University of Texas Southwestern Medical Center, Dallas, Texas 75235, USA.
Am J Physiol. 1999 Aug;277(2):L349-61. doi: 10.1152/ajplung.1999.277.2.L349.
The gene encoding surfactant protein (SP) A, a developmentally regulated pulmonary surfactant-associated protein, is expressed in a lung-specific manner, primarily in pulmonary type II cells. SP-A gene transcription in the rabbit fetal lung is increased by cAMP. To delineate the genomic regions involved in regulation of SP-A gene expression, lines of transgenic mice carrying fusion genes composed of various amounts of 5'-flanking DNA from the rabbit SP-A gene linked to the human growth hormone structural gene as a reporter were established. We found that as little as 378 bp of 5'-flanking DNA was sufficient to direct appropriate lung cell-selective and developmental regulation of transgene expression. The same region was also sufficient to mediate cAMP induction of transgene expression. Mutagenesis or deletion of either of two DNA elements, proximal binding element and a cAMP response element-like sequence, previously found to be crucial for cAMP induction of SP-A promoter activity in transfected type II cells, did not affect lung-selective or temporal regulation of expression of the transgene; however, overall levels of fusion gene expression were reduced compared with those of wild-type transgenes.
编码表面活性蛋白(SP)A的基因是一种受发育调控的肺表面活性物质相关蛋白,以肺特异性方式表达,主要在肺II型细胞中表达。兔胎肺中SP-A基因转录受cAMP增加。为了描绘参与SP-A基因表达调控的基因组区域,建立了携带融合基因的转基因小鼠品系,该融合基因由来自兔SP-A基因的不同量的5'-侧翼DNA与人类生长激素结构基因连接作为报告基因。我们发现,仅378 bp的5'-侧翼DNA就足以指导转基因表达的适当肺细胞选择性和发育调控。同一区域也足以介导cAMP对转基因表达的诱导。先前发现对转染的II型细胞中SP-A启动子活性的cAMP诱导至关重要的两个DNA元件(近端结合元件和cAMP反应元件样序列)中的任何一个发生诱变或缺失,均不影响转基因表达的肺选择性或时间调控;然而,与野生型转基因相比,融合基因表达的总体水平降低了。