Nm-seq maps 2′-O-methytation sites in human mRNA with base precision

被引:207
作者
Dai, Qing [1 ,2 ]
Moshitch-Moshkovitz, Sharon [3 ,4 ]
Han, Dali [1 ,2 ]
Kol, Nitzan [3 ]
Amariglio, Ninette [3 ,4 ,5 ]
Rechavi, Gideon [3 ,4 ,6 ]
Dominissini, Dan [3 ,4 ,6 ]
He, Chuan [1 ,2 ,7 ,8 ]
机构
[1] Univ Chicago, Dept Chem, 5735 S Ellis Ave, Chicago, IL 60637 USA
[2] Univ Chicago, Howard Hughes Med Inst, 5841 S Maryland Ave, Chicago, IL 60637 USA
[3] Chaim Sheba Med Ctr, Canc Res Ctr, Tel Hashomer, Israel
[4] Chaim Sheba Med Ctr, Wohl Ctr Translat Med, Tel Hashomer, Israel
[5] Bar Ilan Univ, Mina & Everard Goodman Fac Life Sci, Ramat Gan, Israel
[6] Tel Aviv Univ, Sackler Sch Med, Tel Aviv, Israel
[7] Univ Chicago, Dept Biochem & Mol Biol, 920 E 58th St, Chicago, IL 60637 USA
[8] Univ Chicago, Inst Biophys Dynam, Chicago, IL 60637 USA
基金
美国国家卫生研究院;
关键词
RIBOSOMAL-RNA; METHYLATION; CAP; THERMODYNAMICS; TRANSLATION; ELIMINATION; BIOGENESIS; COMPLEXES; PROTEINS; SEQUENCE;
D O I
10.1038/nmeth.4294
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The ribose of RNA nucleotides can be 2'-O-methylated (Nm). Despite advances in high-throughput detection, the inert chemical nature of Nm still limits sensitivity and precludes mapping in mRNA. We leveraged the differential reactivity of 2'-O-methylated and 2'-hydroxylated nucleosides to periodate oxidation to develop Nm-seq, a sensitive method for transcriptome-wide mapping of Nm with base precision. Nm-seq uncovered thousands of Nm sites in human mRNA with features suggesting functional roles.
引用
收藏
页码:695 / +
页数:6
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