Kamachi Y, Kondoh H
Department of Molecular Biology, School of Science, Nagoya University, Japan.
Mol Cell Biol. 1993 Sep;13(9):5206-15. doi: 10.1128/mcb.13.9.5206-5215.1993.
Lens-specific expression of the delta 1-crystallin gene is governed by an enhancer in the third intron, and the 30-bp-long DC5 fragment was found to be responsible for eliciting the lens-specific activity. Mutational analysis of the DC5 fragment identified two contiguous, interdependent positive elements and a negative element which overlaps the 3'-located positive element. Previously identified ubiquitous factors delta EF1 bound to the negative element and repressed the enhancer activity in nonlens cells. Mutation and cotransfection analyses indicated the existence of an activator which counteracts the action of delta EF1 in lens cells, probably through binding site competition. We also found a group of nuclear factors, collectively called delta EF2, which bound to the 5'-located positive element. delta EF2a and -b were the major species in lens cells, whereas delta EF2c and -d predominated in nonlens cells. These delta EF2 proteins probably cooperate with factors bound to the 3'-located element in activation in lens cells and repression in nonlens cells. delta EF2 proteins also bound to a promoter sequence of the gamma F-crystallin gene, suggesting that delta EF2 proteins are involved in lens-specific regulation of various crystallin classes.
δ1-晶状体蛋白基因的晶状体特异性表达受第三个内含子中的一个增强子调控,并且发现30bp长的DC5片段负责引发晶状体特异性活性。对DC5片段的突变分析确定了两个相邻的、相互依赖的正调控元件和一个与位于3'端的正调控元件重叠的负调控元件。先前鉴定出的普遍存在的因子δEF1与负调控元件结合,并在非晶状体细胞中抑制增强子活性。突变和共转染分析表明存在一种激活剂,它可能通过结合位点竞争在晶状体细胞中抵消δEF1的作用。我们还发现了一组核因子,统称为δEF2,它们与位于5'端的正调控元件结合。δEF2a和 -b是晶状体细胞中的主要类型,而δEF2c和 -d在非晶状体细胞中占主导。这些δEF2蛋白可能与结合在位于3'端元件上的因子协同作用,在晶状体细胞中激活基因表达,在非晶状体细胞中抑制基因表达。δEF2蛋白也与γF-晶状体蛋白基因的启动子序列结合,这表明δEF2蛋白参与了各种晶状体蛋白类别的晶状体特异性调控。