Smith C I, Rosenberg E, Reisher S R, Li F, Kefalides P, Fisher A B, Feinstein S I
Institute for Environmental Medicine, University of Pennsylvania School of Medicine, Philadelphia 19104-6068, USA.
Am J Physiol. 1995 Nov;269(5 Pt 1):L603-12. doi: 10.1152/ajplung.1995.269.5.L603.
Surfactant protein A (SP-A) is the major pulmonary surfactant protein. We have isolated a rat SP-A genomic clone and determined the sequence from 2.9 kilobases upstream of the transcriptional start through the termination of translation. The exon-intron structure of the rat gene has been determined and compared with the mouse, rabbit, and human genes. We have localized the major transcriptional start site in adult rat lung to nucleotide 30 downstream from the start of the TATA box. Functional mapping indicates that a DNA fragment containing 163 nucleotides upstream of the transcriptional start (-163) can function as a promoter of transcription of a reporter gene in both lung and nonlung derived cell lines. However, the function of this element is weaker in cells of nonlung origin. DNA elements located between -2902 and -163 silence the promoter activity in both lung and nonlung cells. Because the SP-A gene promoter region exhibits limited tissue specificity, the results suggest the existence of other DNA elements which overcome the silencer and confer further lung specificity.
表面活性蛋白A(SP-A)是主要的肺表面活性蛋白。我们分离出了大鼠SP-A基因组克隆,并确定了从转录起始点上游2.9千碱基到翻译终止处的序列。已确定大鼠基因的外显子-内含子结构,并与小鼠、兔子和人类基因进行了比较。我们已将成年大鼠肺中的主要转录起始位点定位到TATA框起始下游的第30个核苷酸处。功能图谱表明,一个包含转录起始点上游163个核苷酸(-163)的DNA片段在肺源性和非肺源性细胞系中均可作为报告基因转录的启动子。然而,该元件在非肺源性细胞中的功能较弱。位于-2902和-163之间的DNA元件会使肺源性和非肺源性细胞中的启动子活性沉默。由于SP-A基因启动子区域表现出有限的组织特异性,这些结果表明存在其他DNA元件,它们可克服沉默子并赋予进一步的肺特异性。