Pazin M J, Kamakaka R T, Kadonaga J T
Department of Biology, University of California, San Diego, La Jolla 92093-0347.
Science. 1994 Dec 23;266(5193):2007-11. doi: 10.1126/science.7801129.
GAL4-VP16-mediated nucleosome reconfiguration and transcriptional activation were observed with preassembled chromatin templates that contained regular and physiological nucleosome spacing. Both processes were dependent on adenosine triphosphate (ATP), although binding of GAL4-VP16 to the chromatin was ATP-independent. Factor-mediated nucleosome reconfiguration was not, however, sufficient for transcriptional activation. These experiments recreate in vitro the active participation of nucleosomal cores in the regulation of transcription that occurs in vivo, and they suggest a multistep pathway for transcriptional activation in which factor- and ATP-dependent nucleosome reconfiguration is followed by facilitation by the DNA-bound activator of transcription from the repressed chromatin template.
利用含有规则且符合生理状态的核小体间距的预组装染色质模板,观察到了GAL4-VP16介导的核小体重构和转录激活。这两个过程均依赖于三磷酸腺苷(ATP),尽管GAL4-VP16与染色质的结合不依赖于ATP。然而,因子介导的核小体重构并不足以实现转录激活。这些实验在体外重现了核小体核心在体内发生的转录调控中的积极参与,并且它们提示了一个转录激活的多步骤途径,其中因子和ATP依赖的核小体重构之后是与DNA结合的激活因子对来自受抑制染色质模板的转录的促进作用。