假尿苷
化学
核糖核酸
滚动圆复制
脱氨基
分子生物学
核糖体RNA
髓系白血病
荧光
生物物理学
计算生物学
生物化学
实时聚合酶链反应
细胞生物学
核酸
DNA
荧光显微镜
分辨率(逻辑)
分子信标
白血病
转移RNA
作者
Xiumin Liu,Jiehua Li,Xiaoyang Duan,Xin Fang,Xiaochen Xue,Shaoqing Han,Xiang Zhou,Wang Yc
标识
DOI:10.1021/acs.analchem.5c08088
摘要
Pseudouridine (Ψ) is a prevalent RNA modification whose site-resolved quantification is critical for understanding epitranscriptomic regulation. We present pseU-SCOPE, a ligation-assisted rolling circle amplification (RCA) assay that converts a bisulfite-derived Ψ signature into a padlock-probe ligation gate, enabling single-nucleotide resolution without qPCR. The workflow supports fluorescence and gel-based, naked-eye readouts following RCA and operates with low RNA input. We validate pseU-SCOPE on established Ψ sites across human rRNAs and mitochondrial tRNAs, generate calibration curves for absolute quantification, and estimate site stoichiometry. Applied to peripheral blood samples, the assay reveals elevated rRNA pseudouridylation in acute myeloid leukemia relative to healthy donors, suggesting disease relevance. Coupled with the deamination mediated by GLORI (glyoxal and nitrite-mediated deamination of unmethylated adenosines), this strategy is adaptable to other RNA modifications such as N 6 -methyladenosine (m 6 A). Together, pseU-SCOPE provides a simple, rapid, qPCR-free, and visual platform for site-specific detection and quantification of RNA modifications, facilitating functional studies and translational research.
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