Webb C F, Eneff K L, Drake F H
Oklahoma Medical Research Foundation, Department of Immunobiology and Cancer, Oklahoma City 73104.
Nucleic Acids Res. 1993 Sep 11;21(18):4363-8. doi: 10.1093/nar/21.18.4363.
We previously identified a B cell-specific protein-DNA complex 5' of an immunoglobulin mu heavy chain promoter. The sequences to which this protein complex bound were required for induction of immunoglobulin mRNA levels with interleukin-5 + antigen. Further studies identified a second sequence 5' of these regulatory sequences that bound to both the nuclear matrix and to a similar interleukin-5 + antigen inducible protein complex. Therefore, we sought to identify the putative regulatory proteins that comprised this DNA-binding complex. In this study, we have used anti-topoisomerase II antibodies to demonstrate that one of the proteins found in the interleukin-5 + antigen inducible complexes is serologically related to topoisomerase II. To our knowledge, this is the first report where a topoisomerase II related protein participates in an inducible mobility shifted protein-DNA complex. These data suggest a model in which the enhanced immunoglobulin gene transcription observed after treatment with interleukin-5 + antigen might be explained by the induction of a protein complex that acts to relieve torsional stress along the gene.
我们之前鉴定出一种位于免疫球蛋白μ重链启动子5'端的B细胞特异性蛋白质-DNA复合物。该蛋白质复合物所结合的序列是白细胞介素-5+抗原诱导免疫球蛋白mRNA水平所必需的。进一步研究在这些调控序列的5'端鉴定出第二个序列,它既能与核基质结合,也能与类似的白细胞介素-5+抗原诱导性蛋白质复合物结合。因此,我们试图鉴定构成这种DNA结合复合物的假定调控蛋白。在本研究中,我们使用抗拓扑异构酶II抗体来证明在白细胞介素-5+抗原诱导复合物中发现的一种蛋白质在血清学上与拓扑异构酶II相关。据我们所知,这是第一份关于拓扑异构酶II相关蛋白参与诱导性迁移率变动蛋白质-DNA复合物的报告。这些数据提示了一个模型,其中用白细胞介素-5+抗原处理后观察到的免疫球蛋白基因转录增强可能是由一种蛋白质复合物的诱导所解释的,该复合物的作用是缓解基因上的扭转应力。