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转录因子IID与启动子DNA结合时近乎零的连接差异。

Near-zero linking difference upon transcription factor IID binding to promoter DNA.

作者信息

Lorch Y, Kornberg R D

机构信息

Department of Cell Biology, Stanford University School of Medicine, California 94305.

出版信息

Mol Cell Biol. 1993 Mar;13(3):1872-5. doi: 10.1128/mcb.13.3.1872-1875.1993.

Abstract

Binding of yeast transcription factor IID (TFIID) to the adenoviral major late promoter in circular DNA molecules caused a linking number change of less than 0.1. TFIID on its own therefore fails to unwind DNA appreciably, or else it causes both unwinding and compensatory writhing. Highly purified, recombinant yeast TFIID relaxed supercoiled DNA, because of a contaminant of bacterial topoisomerase I. Relaxing activity of topoisomerase I was enhanced by the adenoviral major late promoter, suggesting an instability of the TATA sequence or a destabilizing effect on flanking DNA.

摘要

酵母转录因子IID(TFIID)与环状DNA分子中的腺病毒主要晚期启动子结合,导致连接数变化小于0.1。因此,单独的TFIID无法明显解开DNA,否则它会导致解开和补偿性扭曲。由于存在细菌拓扑异构酶I污染物,高度纯化的重组酵母TFIID可使超螺旋DNA松弛。腺病毒主要晚期启动子增强了拓扑异构酶I的松弛活性,这表明TATA序列不稳定或对侧翼DNA有去稳定化作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f772/359500/81f38c678012/molcellb00015-0571-a.jpg

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