Tremethick D, Zucker K, Worcel A
Department of Biology, University of Rochester, New York 14627.
J Biol Chem. 1990 Mar 25;265(9):5014-23.
Assembly of nucleosomes on a 5 S DNA plasmid with histone H3.H4-N1 complex and histone H2A-H2B dimers causes a marked, 30-300-fold repression of 5 S RNA transcription. This repression is a time-dependent process that parallels the process of nucleosome formation. At physiological histone levels, DNA plasmids carrying nucleosomes with only histones H3 and H4 are transcriptionally permissive. The histone H3-H4 chromatin becomes transcriptionally nonpermissive when histone H2A-H2B dimers complement the nucleosome assembly reaction. H3-H4-H2A-H2B nucleosomes, but not H3-H4 nucleosomes, displace a DNA-bound transcription factor IIIA. In contrast, a preassembled 5 S RNA transcription complex is refractory to inactivation by nucleosomes.
在5S DNA质粒上,核小体与组蛋白H3.H4-N1复合物以及组蛋白H2A-H2B二聚体的组装会导致5S RNA转录显著受抑制30至300倍。这种抑制是一个时间依赖性过程,与核小体形成过程平行。在生理组蛋白水平下,携带仅含有组蛋白H3和H4的核小体的DNA质粒在转录上是允许的。当组蛋白H2A-H2B二聚体补充核小体组装反应时,组蛋白H3-H4染色质在转录上变得不允许。H3-H4-H2A-H2B核小体而非H3-H4核小体取代了与DNA结合的转录因子IIIA。相反,预先组装的5S RNA转录复合物对核小体的失活具有抗性。