Woodfine Kathryn, Fiegler Heike, Beare David M, Collins John E, McCann Owen T, Young Bryan D, Debernardi Silvana, Mott Richard, Dunham Ian, Carter Nigel P
The Welcome Trust Sanger Institute, Welcome Genome Campus, Cambridge, UK.
Hum Mol Genet. 2004 Jan 15;13(2):191-202. doi: 10.1093/hmg/ddh016. Epub 2003 Nov 25.
We have developed a directly quantitative method utilizing genomic clone DNA microarrays to assess the replication timing of sequences during the S phase of the cell cycle. The genomic resolution of the replication timing measurements is limited only by the genomic clone size and density. We demonstrate the power of this approach by constructing a genome-wide map of replication timing in human lymphoblastoid cells using an array with clones spaced at 1 Mb intervals and a high-resolution replication timing map of 22q with an array utilizing overlapping sequencing tile path clones. We show a positive correlation, both genome-wide and at a high resolution, between replication timing and a range of genome parameters including GC content, gene density and transcriptional activity.
我们开发了一种直接定量的方法,利用基因组克隆DNA微阵列来评估细胞周期S期序列的复制时间。复制时间测量的基因组分辨率仅受基因组克隆大小和密度的限制。我们通过使用间隔为1 Mb的克隆阵列构建人类淋巴母细胞中复制时间的全基因组图谱,以及使用重叠测序片段路径克隆的阵列构建22q的高分辨率复制时间图谱,证明了这种方法的强大之处。我们在全基因组和高分辨率水平上均显示,复制时间与一系列基因组参数(包括GC含量、基因密度和转录活性)之间存在正相关。