Gregori C, Ginot F, Decaux J F, Weber A, Berbar T, Kahn A, Pichard A L
ICGM, INSERM U. 129 (Laboratoire de Recherches en Génétique et Pathologie Moléculaires), CHU Cochin, Paris, France.
Biochem Biophys Res Commun. 1991 Apr 30;176(2):722-9. doi: 10.1016/s0006-291x(05)80244-x.
The nature and location of the cis-acting DNA sequences regulating expression of the rat aldolase B gene has been investigated. Two liver-specific DNAse I hypersensitive sites were detected, one located just upstream from the cap site, the second in the middle of the first, 4.8-kbp-long, intron. A fragment of 190 bp 5' to the cap site behaved as a tissue-specific but weak core promoter: it directed a detectable reporter gene expression in the Hep G2 cells and hepatocytes, but not in fibroblasts. The tissue-specific expression was stimulated at least 16 fold when constructs contained the entire first intron. The intronic activating sequences could be ascribed to an inner 2 kbp fragment in which the downstream liver-specific DNAse I hypersensitive site was located.
对调控大鼠醛缩酶B基因表达的顺式作用DNA序列的性质和位置进行了研究。检测到两个肝脏特异性的DNA酶I超敏位点,一个位于帽位点上游,另一个位于第一个4.8kbp长的内含子中间。帽位点上游5'端的190bp片段表现为组织特异性但较弱的核心启动子:它在Hep G2细胞和肝细胞中指导可检测的报告基因表达,但在成纤维细胞中则不然。当构建体包含整个第一个内含子时,组织特异性表达至少被刺激16倍。内含子激活序列可归因于一个内部2kbp片段,下游肝脏特异性DNA酶I超敏位点位于该片段中。