Lee M S, Garrard W T
Department of Biochemistry, University of Texas Southwestern Medical Center, Dallas 75235.
EMBO J. 1991 Mar;10(3):607-15. doi: 10.1002/j.1460-2075.1991.tb07988.x.
Utilizing yeast strains containing promoter mutations, we demonstrate that transcription of the HSP82 gene causes nucleosomes toward the 3'-end to become DNase I sensitive and 'split' into structures that exhibit a 'half-nucleosomal' cleavage periodicity. Splitting occurs even when only a few RNA polymerase II molecules are engaged in basal level transcription or during the first round of induced transcription. The split nucleosomal structure survives nuclear isolation suggesting that it may be stabilized by post-translational modifications or non-histone proteins, and may require DNA replication for reversal to a whole nucleosomal structure. Split nucleosomes represent a structure for DNase I sensitive chromatin and are probably of common occurrence but difficult to detect experimentally. We suggest that transient positive supercoils downstream of traversing RNA polymerase lead to nucleosome splitting.
利用含有启动子突变的酵母菌株,我们证明HSP82基因的转录会使朝向3'端的核小体对DNase I敏感,并“分裂”成呈现“半核小体”切割周期性的结构。即使只有少数RNA聚合酶II分子参与基础水平转录或在第一轮诱导转录期间,分裂也会发生。分裂的核小体结构在核分离后仍然存在,这表明它可能通过翻译后修饰或非组蛋白稳定,并且可能需要DNA复制才能恢复为完整的核小体结构。分裂核小体代表了DNase I敏感染色质的一种结构,可能普遍存在但难以通过实验检测到。我们认为,在穿越的RNA聚合酶下游的瞬时正超螺旋会导致核小体分裂。