4.8 Article

Heteromeric RNP Assembly at LINEs Controls Lineage-Specific RNA Processing

期刊

CELL
卷 174, 期 5, 页码 1067-+

出版社

CELL PRESS
DOI: 10.1016/j.cell.2018.07.001

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资金

  1. European Research Council [617837]
  2. Boehringer Ingelheim Fond PhD fellowship
  3. Wellcome Trust [092900, 103760/Z/14/Z, 110292/Z/15/Z, FC001110]
  4. MRC eMedLab Medical Bioinformatics Infrastructure Award [MR/L016311/1]
  5. Okinawa Institute of Science & Technology Graduate University
  6. Cancer Research UK [FC001110]
  7. UK Medical Research Council [FC001110]
  8. Wellcome Trust [110292/Z/15/Z] Funding Source: Wellcome Trust
  9. MRC [MR/L016311/1] Funding Source: UKRI
  10. European Research Council (ERC) [617837] Funding Source: European Research Council (ERC)

向作者/读者索取更多资源

Long mammalian introns make it challenging for the RNA processing machinery to identify exons accurately. We find that LINE-derived sequences (LINEs) contribute to this selection by recruiting dozens of RNA-binding proteins (RBPs) to introns. This includes MATR3, which promotes binding of PTBP1 to multivalent binding sites within LINEs. Both RBPs repress splicing and 3 ' end processing within and around LINEs. Notably, repressive RBPs preferentially bind to evolutionarily young LINEs, which are located far from exons. These RBPs insulate the LINEs and the surrounding intronic regions from RNA processing. Upon evolutionary divergence, changes in RNA motifs within LINEs lead to gradual loss of their insulation. Hence, older LINEs are located closer to exons, are a common source of tissue-specific exons, and increasingly bind to RBPs that enhance RNA processing. Thus, LINEs are hubs for the assembly of repressive RBPs and also contribute to the evolution of new, lineage-specific transcripts in mammals.

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