Abstract
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 (m7G)-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 m7G-capped pre-miRNAs genome wide. The m 7G-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. © 2013 Elsevier Inc.
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CITATION STYLE
Xie, M., Li, M., Vilborg, A., Lee, N., Shu, M. D., Yartseva, V., … Steitz, J. A. (2013). Mammalian 5′-capped microRNA precursors that generate a single microRNA. Cell, 155(7), 1568–1580. https://doi.org/10.1016/j.cell.2013.11.027
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