期刊
JOURNAL OF CELL SCIENCE
卷 125, 期 11, 页码 2709-2720出版社
COMPANY BIOLOGISTS LTD
DOI: 10.1242/jcs.100354
关键词
Intranuclear RNA trafficking; Transcription sites; microRNA; Nuclear architecture; pri-miRNA processing; DGCR8-Drosha (Microprocessor) complex
类别
资金
- European Molecular Biology Organization (EMBO Young Investigator Programme)
- Agence National pour la Recherche (ANR-ImpmiR)
- Association pour la Recherche sur le Cancer (ARC)
- Ligue Regionale contre le Cancer
- PhD fellowship from the RegRNA program of the Paul Sabatier University (AOCS)
Nuclear primary microRNA (pri-miRNA) processing catalyzed by the DGCR8-Drosha (Microprocessor) complex is highly regulated. Little is known, however, about how microRNA biogenesis is spatially organized within the mammalian nucleus. Here, we image for the first time, in living cells and at the level of a single microRNA cluster, the intranuclear distribution of untagged, endogenously-expressed pri-miRNAs generated at the human imprinted chromosome 19 microRNA cluster (C19MC), from the environment of transcription sites to single molecules of fully released DGCR8-bound pri-miRNAs dispersed throughout the nucleoplasm. We report that a large fraction of Microprocessor concentrates onto unspliced C19MC pri-miRNA deposited in close proximity to their genes. Our live-cell imaging studies provide direct visual evidence that DGCR8 and Drosha are targeted post-transcriptionally to C19MC pri-miRNAs as a preformed complex but dissociate separately. These dynamics support the view that, upon pri-miRNA loading and most probably concomitantly with Drosha-mediated cleavages, Microprocessor undergoes conformational changes that trigger the release of Drosha while DGCR8 remains stably bound to pri-miRNA.
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