Knezetic J A, Luse D S
Cell. 1986 Apr 11;45(1):95-104. doi: 10.1016/0092-8674(86)90541-6.
RNA was synthesized in vitro using HeLa cell nuclear extracts and circular DNA templates onto which varying numbers of nucleosomes had been reconstituted with Xenopus oocyte extracts. We found that fully reconstituted templates supported no specific initiation by RNA polymerase II; however, DNA exposed to the reconstitution extracts under conditions which did not allow nucleosome deposition was transcribed normally. A set of successively less reconstituted templates was also transcribed. No initiation occurred on reconstitutes with more than two-thirds of the physiological nucleosome density; reconstitutes with less than one-third of the physiological nucleosome density were transcribed as efficiently as naked DNA.
使用HeLa细胞核提取物和环状DNA模板在体外合成RNA,这些环状DNA模板已用非洲爪蟾卵母细胞提取物重建了不同数量的核小体。我们发现,完全重建的模板不支持RNA聚合酶II的特异性起始;然而,在不允许核小体沉积的条件下暴露于重建提取物的DNA能正常转录。还转录了一组连续重建程度较低的模板。在核小体密度超过生理密度三分之二的重建模板上没有发生起始;核小体密度低于生理密度三分之一的重建模板转录效率与裸露DNA一样高。