小RNA
诱饵
计算生物学
功能(生物学)
生物
细胞生物学
基因
遗传学
受体
作者
Gavriel Mullokandov,Alessia Baccarini,Albert Ruzo,Anitha D. Jayaprakash,Navpreet Tung,Benjamin Israelow,Matthew J. Evans,Ravi Sachidanandam,Brian D. Brown
出处
期刊:Nature Methods
[Nature Portfolio]
日期:2012-07-01
卷期号:9 (8): 840-846
被引量:375
摘要
Two large-scale resources for studying microRNA function are presented: one is a library of fluorescent sensors with a corresponding assay for global profiling of microRNA activity in different cell types; the other is a decoy library for suppressing microRNA activity individually or in pooled loss-of-function screens. We introduce two large-scale resources for functional analysis of microRNA (miRNA): a decoy library for inhibiting miRNA function and a sensor library for monitoring microRNA activity. To take advantage of the sensor library, we developed a high-throughput assay called Sensor-seq to simultaneously quantify the activity of hundreds of miRNAs. Using this approach, we show that only the most abundant miRNAs in a cell mediate target suppression. Over 60% of detected miRNAs had no discernible activity, which indicated that the functional 'miRNome' of a cell is considerably smaller than currently inferred from profiling studies. Moreover, some highly expressed miRNAs exhibited relatively weak activity, which in some cases correlated with a high target-to-miRNA ratio or increased nuclear localization of the miRNA. Finally, we show that the miRNA decoy library can be used for pooled loss-of-function studies. These tools are valuable resources for studying miRNA biology and for miRNA-based therapeutics.
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