Ljungman M, Hanawalt P C
Department of Radiation Oncology, University of Michigan Medical Center, Ann Arbor 48109-0582, USA.
Nucleic Acids Res. 1995 May 25;23(10):1782-9. doi: 10.1093/nar/23.10.1782.
DNA topology has been suggested to play an important role in the process of transcription. Negative torsional tension has been shown to stimulate both pre-initiation complex formation and promoter clearance on plasmid DNA in vitro. We recently showed that genomic DNA in human cells contains localized torsional tension. In the present study we have further characterized and mapped torsional tension in the dihydrofolate reductase (DHFR) gene in Chinese hamster ovary (CHO) cells and investigated the effects of differential rates of transcription on the magnitude and location of this tension. Using psoralen photo-cross-linking in conjunction with X-irradiation, we found that relaxable psoralen hypersensitivity was specifically localized to the promoter region of the serum-regulated DHFR gene in serum-stimulated, but not in serum-starved, cells. Moreover, this hypersensitivity did not appear to be caused by transcription elongation, since it persisted in cells in which transcription of the DHFR gene had been reduced by the transcription inhibitor 5,6-dichloro-1-beta-D-ribofurano-sylbenzimidazole (DRB). We suggest that the generation of negative torsional tension in DNA may play an important role in gene regulation by poising genes for transcription.
有人提出DNA拓扑结构在转录过程中起重要作用。体外实验表明,负性扭转张力可刺激质粒DNA上起始前复合物的形成及启动子清除。我们最近发现,人类细胞中的基因组DNA含有局部扭转张力。在本研究中,我们进一步对中国仓鼠卵巢(CHO)细胞中二氢叶酸还原酶(DHFR)基因的扭转张力进行了表征和定位,并研究了不同转录速率对这种张力大小和位置的影响。通过将补骨脂素光交联与X射线照射相结合,我们发现,可松弛的补骨脂素超敏反应特异性定位于血清刺激的细胞中血清调节的DHFR基因的启动子区域,而在血清饥饿的细胞中则没有。此外,这种超敏反应似乎不是由转录延伸引起的,因为它在DHFR基因转录已被转录抑制剂5,6-二氯-1-β-D-呋喃核糖基苯并咪唑(DRB)降低的细胞中持续存在。我们认为,DNA中负性扭转张力的产生可能通过使基因处于转录准备状态而在基因调控中起重要作用。