Department of Biochemistry, Stanford University, Stanford, United States.
Department of Biology, Stanford University, Stanford, United States.
Elife. 2018 Apr 12;7:e27024. doi: 10.7554/eLife.27024.
RNA is a critical component of chromatin in eukaryotes, both as a product of transcription, and as an essential constituent of ribonucleoprotein complexes that regulate both local and global chromatin states. Here, we present a proximity ligation and sequencing method called romatin-ssociated NA uencing (ChAR-seq) that maps all RNA-to-DNA contacts across the genome. Using cells, we show that ChAR-seq provides unbiased, de novo identification of targets of chromatin-bound RNAs including nascent transcripts, chromosome-specific dosage compensation ncRNAs, and genome-wide trans-associated RNAs involved in co-transcriptional RNA processing.
RNA 是真核生物染色质的关键组成部分,既是转录的产物,也是调节局部和全局染色质状态的核蛋白复合物的必需成分。在这里,我们提出了一种称为 romatin-ssociated NA uencing(ChAR-seq)的邻近连接和测序方法,该方法可以绘制整个基因组上的所有 RNA-DNA 接触点。使用 细胞,我们表明 ChAR-seq 提供了染色质结合 RNA 靶点的无偏、从头鉴定,包括新生转录物、染色体特异性剂量补偿 ncRNA 以及涉及共转录 RNA 加工的全基因组转关联 RNA。