Mammalian 5′-Capped MicroRNA Precursors that Generate a SingleMicroRNA

被引:190
作者
Xie, Mingyi [1 ]
Li, Mingfeng [2 ]
Vilborg, Anna [1 ]
Lee, Nara [1 ]
Shu, Mei-Di [1 ]
Yartseva, Valeria [3 ]
Sestan, Nenad [2 ]
Steitz, Joan A. [1 ]
机构
[1] Yale Univ, Sch Med, Boyer Ctr Mol Med, Dept Mol Biophys & Biochem,Howard Hughes Med Inst, New Haven, CT 06536 USA
[2] Yale Univ, Sch Med, Dept Neurobiol, Kavli Inst Neurosci, New Haven, CT 06510 USA
[3] Yale Univ, Sch Med, Dept Genet, New Haven, CT 06510 USA
基金
美国国家卫生研究院;
关键词
RNA-POLYMERASE-II; EMBRYONIC STEM-CELLS; NUCLEAR EXPORT; HERPESVIRUS USES; VIRAL MICRORNAS; MESSENGER-RNAS; IN-VIVO; BIOGENESIS; PATHWAY; EXPRESSION;
D O I
10.1016/j.cell.2013.11.027
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MicroRNAs (miRNAs) are short RNA gene regulators typically produced from primary transcripts that are cleaved by the nuclear microprocessor complex, with the resulting precursor miRNA hairpins exported by exportin 5 and processed by cytoplasmic Dicer to yield two (5p and 3p) miRNAs. Here, we document microprocessor-independent 7-methylguanosine (m(7)G)-capped pre-miRNAs, whose 5' ends coincide with transcription start sites and 3' ends are most likely generated by transcription termination. By establishing a small RNA Cap-seq method that employs the cap-binding protein eIF4E, we identified a group of murine m(7)G-capped pre-miRNAs genome wide. The m(7)G-capped pre-miRNAs are exported via the PHAX-exportin 1 pathway. After Dicer cleavage, only the 3p-miRNA is efficiently loaded onto Argonaute to form a functional microRNP. This unusual miRNA biogenesis pathway, which differs in pre-miRNA synthesis, nuclear-cytoplasmic transport, and guide strand selection, enables the development of shRNA expression constructs that produce a single 3p-siRNA.
引用
收藏
页码:1568 / 1580
页数:13
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