Liu Q R, Tini M, Tsui L C, Breitman M L
Division of Molecular and Developmental Biology, Samuel Lunenfeld Research Institute, Mount Sinai Hospital, Toronto, Ontario, Canada.
Mol Cell Biol. 1991 Mar;11(3):1531-7. doi: 10.1128/mcb.11.3.1531-1537.1991.
The elements regulating lens-specific expression of the mouse gamma F-crystallin gene were examined. Here we show that mouse gamma F-crystallin sequences -67 to +45 contain a low basal level of lens-specific promoter activity and that sequences -67 to -25, which are highly conserved among different gamma-crystallin genes, are able to function as a strong transcriptional activator when duplicated and placed upstream of the TATA box. We also show that nuclear factors from lens and nonlens cells are able to form different complexes with sequences centered at -46 to -36 and demonstrate that binding of the factor from lens cells correlates with lens-specific promoter activity of the mouse gamma F-crystallin gene.
对调控小鼠γF-晶体蛋白基因晶状体特异性表达的元件进行了研究。在此我们表明,小鼠γF-晶体蛋白基因序列-67至+45具有低水平的晶状体特异性启动子活性,而在不同γ-晶体蛋白基因中高度保守的序列-67至-25,当重复并置于TATA框上游时,能够作为一种强大的转录激活因子发挥作用。我们还表明,来自晶状体和非晶状体细胞的核因子能够与以-46至-36为中心的序列形成不同的复合物,并证明来自晶状体细胞的因子的结合与小鼠γF-晶体蛋白基因的晶状体特异性启动子活性相关。