4.8 Article

Mammalian 5′-Capped MicroRNA Precursors that Generate a SingleMicroRNA

Journal

CELL
Volume 155, Issue 7, Pages 1568-1580

Publisher

CELL PRESS
DOI: 10.1016/j.cell.2013.11.027

Keywords

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Funding

  1. National Institutes of Health [CA16038, MH081896]
  2. Leukemia and Lymphoma Society [5416-13]
  3. Wenner-Gren Foundations
  4. Swedish Society for Medical Research

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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.

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