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果蝇肌动蛋白和Hsp70热休克基因上拓扑异构酶I和II切割位点的分析。

Analysis of topoisomerase I and II cleavage sites on the Drosophila actin and Hsp70 heat shock genes.

作者信息

Kroeger P E, Rowe T C

机构信息

Department of Pharmacology and Therapeutics, University of Florida College of Medicine, Gainesville 32610-0267.

出版信息

Biochemistry. 1992 Mar 10;31(9):2492-501. doi: 10.1021/bi00124a008.

Abstract

We have compared topoisomerase I and II cleavage sites on the actin 5C and 57A genes and the hsp70 genes in Drosophila Kc cells using the inhibitors camptothecin (topoisomerase I specific) and VM-26 (topoisomerase II specific) to assess the role of these enzymes in transcriptional regulation. Topoisomerase I cleavage sites were localized to the transcribed regions of the actin 5C and hsp70 genes and were present only when these genes were active. The actin 57A gene, shown previously to be inactive in Kc cells, had no detectable topoisomerase I cleavage sites. In contrast to topoisomerase I, topoisomerase II cleavage sites could be detected on transcriptionally active and inactive actin and hsp70 DNA sequences. Topoisomerase II cleavage sites on the inactive hsp70 gene were primarily localized to the very 5' end of the transcribed region of the gene. However, upon heat-induced activation of hsp70 transcription, topoisomerase II cleavage rapidly shifted from the 5' to the 3' end of the gene. Then, during the shutdown of hsp70 expression, there was a gradual reappearance of topoisomerase II cleavage at the 5' end of the gene that temporally correlated with the repression of hsp70 transcription. There was a similar preferential association of topoisomerase II with the 5' ends of transcriptionally repressed actin 5C and 57A genes. These results demonstrate that there are marked differences in how topoisomerases I and II interact with transcriptionally active and inactive regions of chromatin. In addition, we have identified an unusual type of topoisomerase II binding site that is preferentially associated with the 5' ends of inactive hsp70 and actin genes, suggesting that this enzyme may facilitate changes in chromatin structure that are associated with repression of gene transcription.

摘要

我们使用喜树碱(拓扑异构酶I特异性抑制剂)和VM - 26(拓扑异构酶II特异性抑制剂),比较了果蝇Kc细胞中肌动蛋白5C和57A基因以及热休克蛋白70(hsp70)基因上的拓扑异构酶I和II的切割位点,以评估这些酶在转录调控中的作用。拓扑异构酶I的切割位点定位于肌动蛋白5C和hsp70基因的转录区域,并且仅在这些基因活跃时出现。先前显示在Kc细胞中无活性的肌动蛋白57A基因,未检测到拓扑异构酶I的切割位点。与拓扑异构酶I相反,在转录活跃和不活跃的肌动蛋白及hsp70 DNA序列上均可检测到拓扑异构酶II的切割位点。不活跃的hsp70基因上的拓扑异构酶II切割位点主要定位于该基因转录区域的5'端。然而,在热诱导hsp70转录激活后,拓扑异构酶II的切割迅速从基因的5'端转移至3'端。然后,在hsp70表达关闭期间,拓扑异构酶II在基因5'端的切割逐渐重新出现,这在时间上与hsp70转录的抑制相关。拓扑异构酶II与转录受抑制的肌动蛋白5C和57A基因的5'端也有类似的优先结合。这些结果表明,拓扑异构酶I和II与染色质转录活跃和不活跃区域相互作用的方式存在显著差异。此外,我们鉴定出一种不寻常的拓扑异构酶II结合位点,其优先与不活跃的hsp70和肌动蛋白基因的5'端相关联,这表明该酶可能促进与基因转录抑制相关的染色质结构变化。

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