Hirose S, Suzuki Y
Department of Developmental Biology, National Institute for Basic Biology, Okazaki, Japan.
Proc Natl Acad Sci U S A. 1988 Feb;85(3):718-22. doi: 10.1073/pnas.85.3.718.
In a posterior silk gland extract, covalently closed circular (ccc) DNA is in a superhelical state that supports more transcription of fibroin gene than does linear DNA. A HeLa cell extract showed neither the supercoiling activity nor the preference for the transcription of ccc DNA over linear DNA. These activities could be added to the HeLa cell extract. Phosphocellulose fractionation of the posterior silk gland extract yielded a flow-through fraction and a 0.6 M KCl eluate fraction that were required for the supercoiling and for the efficient transcription of the ccc template in the acceptor HeLa cell extract. The 0.6 M KCl fraction had a DNA topoisomerase II activity, and the flow-through fraction contained a supercoiling factor that, with the aid of topoisomerase II, introduced negative supercoils into ccc DNA. When both fractions were added to the posterior silk gland extract, more supercoiling occurred than with the extract alone. Several genes were optimally transcribed under various extents of supercoiling. The fibroin gene and adenovirus 2 major late promoter were fully transcribed as partially supercoiled templates. The sericin gene required more supercoiling for full transcription, whereas no preference for supercoiling was seen with the transcription of hsp70. These results suggest that DNA topology plays a role in the regulation of gene expression.
在后丝腺提取物中,共价闭合环状(ccc)DNA处于超螺旋状态,与线性DNA相比,它能支持更多的丝心蛋白基因转录。HeLa细胞提取物既没有超螺旋活性,也没有对ccc DNA转录优于线性DNA的偏好。这些活性可以添加到HeLa细胞提取物中。后丝腺提取物的磷酸纤维素分级分离产生了一个流穿级分和一个0.6M KCl洗脱级分,它们是超螺旋和受体HeLa细胞提取物中ccc模板高效转录所必需的。0.6M KCl级分具有DNA拓扑异构酶II活性,流穿级分含有一种超螺旋因子,该因子在拓扑异构酶II的帮助下将负超螺旋引入ccc DNA。当将这两个级分都添加到后丝腺提取物中时,超螺旋比单独使用提取物时更多。几个基因在不同程度的超螺旋下被最佳转录。丝心蛋白基因和腺病毒2主要晚期启动子作为部分超螺旋模板被完全转录。丝胶蛋白基因需要更多的超螺旋才能完全转录,而hsp70转录对超螺旋没有偏好。这些结果表明DNA拓扑结构在基因表达调控中起作用。