O'Neill T E, Meersseman G, Pennings S, Bradbury E M
Department of Biological Chemistry, School of Medicine, University of California, Davis 95616, USA.
Nucleic Acids Res. 1995 Mar 25;23(6):1075-82. doi: 10.1093/nar/23.6.1075.
The effect of histone H1 on transcription by bacteriophage T7 RNA polymerase was examined using reconstituted chromatin templates. A 3.8 kb linear DNA template consisting of a specific transcription promoter for T7 RNA polymerase placed upstream of 18 tandem repeats of a 207 bp nucleosome positioning sequence derived from the 5S rRNA gene of Lytechinus variegatus was used as a template for chromatin reconstitution. Regularly spaced arrays of nucleosome cores were assembled onto this DNA template from donor histone octamers by salt step dialysis. Histone H1 was incorporated onto free DNA or reconstituted chromatin templates and double label transcription assays were performed. The experiments indicated that histone H1 has a strong inhibitory effect on both transcription initiation and elongation. These effects are especially pronounced on chromatin templates, where both transcription initiation and elongation are virtually halted. The inhibition of transcription elongation appears to result from a dramatic increase in premature termination of transcripts. These experiments indicate that assembly of histone H1 into chromatin can result in structures which are completely repressed with respect to transcription.
利用重组染色质模板研究了组蛋白H1对噬菌体T7 RNA聚合酶转录的影响。一个3.8 kb的线性DNA模板被用作染色质重组的模板,该模板由T7 RNA聚合酶的特定转录启动子组成,该启动子位于来自多棘海胆5S rRNA基因的207 bp核小体定位序列的18个串联重复序列的上游。通过盐步透析将规则间隔排列的核小体核心从供体组蛋白八聚体组装到该DNA模板上。将组蛋白H1掺入游离DNA或重组染色质模板中,并进行双标记转录分析。实验表明,组蛋白H1对转录起始和延伸均有强烈的抑制作用。这些作用在染色质模板上尤为明显,在染色质模板上转录起始和延伸实际上都停止了。转录延伸的抑制似乎是由于转录本过早终止的显著增加所致。这些实验表明,组蛋白H1组装到染色质中可导致相对于转录完全被抑制的结构。