Scott R S, Truong K Y, Vos J M
Department of Biochemistry and Biophysics, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-7295, USA.
Nucleic Acids Res. 1997 Nov 15;25(22):4505-12. doi: 10.1093/nar/25.22.4505.
Replication of the 400 copies of the 43 kb human ribosomal RNA (rDNA) locus spans most of the S phase. To examine the basis for the unusual pattern of rDNA replication, a sensitive strategy was developed to map origins of DNA replication and measure apparent rates of fork progression within a chromosomal locus. This technique, termed differential intragenomic replication timing, revealed that initiation within the actively transcribed rDNA occurred in early S within a 10.7 kb region spanning the promoter and 5' external transcribed spacer. Forks emanating from this early bidirectional origin progressed at an apparent slow rate with the sense and anti-sense forks moving at 0.32 and 0.23 kb/min. Using a photochemical-based technique, the chromatin status of the rDNA repeats was assayed throughout the S phase. Approximately 85% of the rDNA repeats were in a transcriptionally active chromatin structure at the start of S phase. A progressive decrease in the transcription state of the rDNA loci was observed, reaching a minimum between 3 and 6 h in mid S phase. Altogether, the data suggest a link between RNA polymerase I mediated transcription and site-specific initiation of DNA replication within the rDNA multicopy locus.
43 kb人类核糖体RNA(rDNA)基因座的400个拷贝的复制跨越了大部分S期。为了研究rDNA复制异常模式的基础,开发了一种灵敏的策略来绘制DNA复制起点并测量染色体基因座内叉进展的表观速率。这种技术称为差异基因组内复制时间,揭示了在活跃转录的rDNA内的起始发生在早期S期,在一个跨越启动子和5'外部转录间隔区的10.7 kb区域内。从这个早期双向起点发出的叉以明显缓慢的速率进展,正义叉和反义叉分别以0.32和0.23 kb/分钟移动。使用基于光化学的技术,在整个S期测定rDNA重复序列的染色质状态。在S期开始时,大约85%的rDNA重复序列处于转录活跃的染色质结构中。观察到rDNA基因座的转录状态逐渐下降,在S期中期3至6小时达到最低。总之,数据表明RNA聚合酶I介导的转录与rDNA多拷贝基因座内DNA复制的位点特异性起始之间存在联系。