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10.1038/nsmb.2982

http://scihub22266oqcxt.onion/10.1038/nsmb.2982
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suck abstract from ncbi


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pmid25730776
      Nat+Struct+Mol+Biol 2015 ; 22 (4 ): 319-27
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  • Microprocessor mediates transcriptional termination of long noncoding RNA transcripts hosting microRNAs #MMPMID25730776
  • Dhir A ; Dhir S ; Proudfoot NJ ; Jopling CL
  • Nat Struct Mol Biol 2015[Apr]; 22 (4 ): 319-27 PMID25730776 show ga
  • MicroRNAs (miRNAs) play a major part in the post-transcriptional regulation of gene expression. Mammalian miRNA biogenesis begins with cotranscriptional cleavage of RNA polymerase II (Pol II) transcripts by the Microprocessor complex. Although most miRNAs are located within introns of protein-coding transcripts, a substantial minority of miRNAs originate from long noncoding (lnc) RNAs, for which transcript processing is largely uncharacterized. We show, by detailed characterization of liver-specific lnc-pri-miR-122 and genome-wide analysis in human cell lines, that most lncRNA transcripts containing miRNAs (lnc-pri-miRNAs) do not use the canonical cleavage-and-polyadenylation pathway but instead use Microprocessor cleavage to terminate transcription. Microprocessor inactivation leads to extensive transcriptional readthrough of lnc-pri-miRNA and transcriptional interference with downstream genes. Consequently we define a new RNase III-mediated, polyadenylation-independent mechanism of Pol II transcription termination in mammalian cells.
  • |*Models, Genetic [MESH]
  • |*RNA Processing, Post-Transcriptional [MESH]
  • |*Transcription, Genetic [MESH]
  • |Gene Expression Regulation [MESH]
  • |HeLa Cells [MESH]
  • |Humans [MESH]
  • |MicroRNAs/chemistry/*metabolism [MESH]


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