首页> 外文期刊>Journal of Molecular Biology >Nucleosome dynamics. II. High flexibility of nucleosome entering and exiting DNAs to positive crossing. An ethidium bromide fluorescence study of mononucleosomes on DNA minicircles.
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Nucleosome dynamics. II. High flexibility of nucleosome entering and exiting DNAs to positive crossing. An ethidium bromide fluorescence study of mononucleosomes on DNA minicircles.

机译:核小体动力学。二。核小体进入和离开DNA进行正向杂交的高度灵活性。 DNA小环上单核小体的溴化乙锭荧光研究。

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摘要

H2A-H2B exchange with the intranuclear histone pool upon chromatin transcription in vivo is generally viewed as being triggered by the DNA positive supercoiling wave pushed by the elongating polymerase. This notion was tested here by investigating a potential release of H2A-H2B by ethidium bromide-induced positive supercoiling in the loop of mononucleosomes reconstituted on DNA minicircles. The results of gel electrophoresis, fluorescence titration and electron microscopy showed that such a positive supercoiling was not able to release H2A-H2B, nor to unfold the nucleosome to any detectable extent. The reason appeared to be the ease with which the loop could undergo a positive crossing, a surprising observation in view of the DNA left-handed wrapping around the octamer. Moreover, the influence of histone acetylation suggested that such loop flexibility to positive crossing is mediated by histone N-terminal tails which, by interacting with entering and exiting DNAs, reduce their electrostatic repulsion. These conclusions are confirmed and extended in the accompanying article through relaxation with topoisomerase I. Copyright 1999 Academic Press.
机译:在体内染色质转录后,与核内组蛋白池进行H2A-H2B交换通常被认为是由延伸聚合酶推动的DNA阳性超螺旋波触发的。在此通过研究溴化乙锭诱导的在DNA小环上重建的单核小体环中的正超螺旋作用释放H2A-H2B的可能性来测试此概念。凝胶电泳,荧光滴定和电子显微镜的结果表明,这种阳性超螺旋不能释放H2A-H2B,也不能将核小体展开到任何可检测的程度。原因似乎是环易于经历正向杂交,考虑到DNA左旋包裹在八聚体上,这一发现令人惊讶。而且,组蛋白乙酰化的影响表明,这种对正相交的环柔性是由组蛋白N-末端尾部介导的,其通过与进入和离开的DNA相互作用而减少了它们的静电排斥力。通过使用拓扑异构酶I放松,这些结论在随附的文章中得到了证实和扩展。版权所有1999,Academic Press。

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