生物
环状RNA
计算生物学
核糖核酸
基因
遗传学
环状DNA
进化生物学
基因组
作者
Josh N. Vo,Marcin Cieślik,Yajia Zhang,Sudhanshu Shukla,Lanbo Xiao,Yuping Zhang,Yi‐Mi Wu,Saravana M. Dhanasekaran,Carl G. Engelke,Xuhong Cao,Dan R. Robinson,Alexey I. Nesvizhskii,Arul M. Chinnaiyan
出处
期刊:Cell
[Cell Press]
日期:2019-02-01
卷期号:176 (4): 869-881.e13
被引量:1984
标识
DOI:10.1016/j.cell.2018.12.021
摘要
Circular RNAs (circRNAs) are an intriguing class of RNA due to their covalently closed structure, high stability, and implicated roles in gene regulation. Here, we used an exome capture RNA sequencing protocol to detect and characterize circRNAs across >2,000 cancer samples. When compared against Ribo-Zero and RNase R, capture sequencing significantly enhanced the enrichment of circRNAs and preserved accurate circular-to-linear ratios. Using capture sequencing, we built the most comprehensive catalog of circRNA species to date: MiOncoCirc, the first database to be composed primarily of circRNAs directly detected in tumor tissues. Using MiOncoCirc, we identified candidate circRNAs to serve as biomarkers for prostate cancer and were able to detect circRNAs in urine. We further detected a novel class of circular transcripts, termed read-through circRNAs, that involved exons originating from different genes. MiOncoCirc will serve as a valuable resource for the development of circRNAs as diagnostic or therapeutic targets across cancer types.
科研通智能强力驱动
Strongly Powered by AbleSci AI