Swamynathan Shivalingappa K, Piatigorsky Joram
Laboratory of Molecular and Developmental Biology, NEI/National Institutes of Health, Bldg. 6 Rm. 201, 6 Center Drive, Bethesda, MD 20892, USA.
J Biol Chem. 2002 Dec 20;277(51):49700-6. doi: 10.1074/jbc.M209700200. Epub 2002 Oct 25.
The mouse Shsp/alphaB-crystallin and Mkbp/HspB2 genes are closely linked and divergently transcribed. In this study, we have analyzed the contribution of the intergenic enhancer to Shsp/alphaB-crystallin and Mkbp/HspB2 promoter activity using dual-reporter vectors in transient transfection and transgenic mouse experiments. Deletion of the enhancer reduced Shsp/alphaB-crystallin promoter activity by 30- and 93-fold and Mkbp/HspB2 promoter activity by 6- and 10-fold in transiently transfected mouse lens alpha-TN4 and myoblast C2C12 cells, respectively. Surprisingly, inversion of the enhancer reduced Shsp/alphaB-crystallin promoter activity by 17-fold, but did not affect Mkbp/HspB2 promoter activity in the transfected cells. In contrast, enhancer activity was orientation-independent in combination with a heterologous promoter in transfected cells. Transgenic mouse experiments established the orientation dependence and Shsp/alphaB-crystallin promoter preference of the intergenic enhancer in its native context. The orientation dependence and preferential effect of the Shsp/alphaB-crystallin enhancer on the Shsp/alphaB-crystallin promoter provide an example of adaptive changes in gene regulation accompanying the functional diversification of duplicated genes during evolution.
小鼠的Shsp/αB-晶状体蛋白基因和Mkbp/HspB2基因紧密连锁且转录方向相反。在本研究中,我们利用双报告载体,通过瞬时转染和转基因小鼠实验,分析了基因间增强子对Shsp/αB-晶状体蛋白和Mkbp/HspB2启动子活性的作用。在瞬时转染的小鼠晶状体α-TN4细胞和成肌细胞C2C12细胞中,增强子的缺失分别使Shsp/αB-晶状体蛋白启动子活性降低30倍和93倍,使Mkbp/HspB2启动子活性降低6倍和10倍。令人惊讶的是,增强子的倒置使转染细胞中Shsp/αB-晶状体蛋白启动子活性降低了17倍,但不影响Mkbp/HspB2启动子活性。相反,在转染细胞中,增强子与异源启动子结合时活性不受方向影响。转基因小鼠实验证实了在其天然环境中基因间增强子的方向依赖性以及对Shsp/αB-晶状体蛋白启动子的偏好性。Shsp/αB-晶状体蛋白增强子对Shsp/αB-晶状体蛋白启动子的方向依赖性和优先效应,为进化过程中伴随重复基因功能多样化的基因调控适应性变化提供了一个例子。