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The Augmented R-Loop Is a Unifying Mechanism for Myelodysplastic Syndromes Induced by High-Risk Splicing Factor Mutations.

Molecular cell | 2018

Mutations in several general pre-mRNA splicing factors have been linked to myelodysplastic syndromes (MDSs) and solid tumors. These mutations have generally been assumed to cause disease by the resultant splicing defects, but different mutations appear to induce distinct splicing defects, raising the possibility that an alternative common mechanism is involved. Here we report a chain of events triggered by multiple splicing factor mutations, especially high-risk alleles in SRSF2 and U2AF1, including elevated R-loops, replication stress, and activation of the ataxia telangiectasia and Rad3-related protein (ATR)-Chk1 pathway. We further demonstrate that enhanced R-loops, opposite to the expectation from gained RNA binding with mutant SRSF2, result from impaired transcription pause release because the mutant protein loses its ability to extract the RNA polymerase II (Pol II) C-terminal domain (CTD) kinase-the positive transcription elongation factor complex (P-TEFb)-from the 7SK complex. Enhanced R-loops are linked to compromised proliferation of bone-marrow-derived blood progenitors, which can be partially rescued by RNase H overexpression, suggesting a direct contribution of augmented R-loops to the MDS phenotype.

Pubmed ID: 29395063 RIS Download

Associated grants

  • Agency: NIGMS NIH HHS, United States
    Id: R01 GM052872
  • Agency: NIDDK NIH HHS, United States
    Id: R01 DK098808
  • Agency: NCI NIH HHS, United States
    Id: P30 CA008748
  • Agency: NHGRI NIH HHS, United States
    Id: R01 HG004659
  • Agency: NIGMS NIH HHS, United States
    Id: R01 GM049369

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This is a list of tools and resources that we have found mentioned in this publication.


SAM format (tool)

RRID:SCR_012093

A generic alignment format for storing read alignments against reference sequences, supporting short and long reads (up to 128 Mbp) produced by different sequencing platforms.

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Bowtie 2 (tool)

RRID:SCR_016368

Ultrafast and memory efficient tool for aligning sequencing reads to long reference sequences. Supports gapped, local, and paired end alignment modes. More suited to finding longer, gapped alignments in comparison with original Bowtie method.

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Bowtie (tool)

RRID:SCR_005476

Software ultrafast memory efficient tool for aligning sequencing reads. Bowtie is short read aligner.

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Anti-DNA-RNA Hybrid [S9.6] Antibody (antibody)

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POLR2AphosphoS2-human (antibody)

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This polyclonal targets POLR2AphosphoS2

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HEXIM1 Antibody (antibody)

RRID:AB_10892626

This unknown targets HEXIM1

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HEXIM1 Antibody (antibody)

RRID:AB_10893099

This unknown targets HEXIM1

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CDK9 (C12F7) (antibody)

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This monoclonal targets CDK9

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RPA32 Antibody (antibody)

RRID:AB_185548

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Phospho RPA32 (S4/S8) Antibody (antibody)

RRID:AB_210547

This unknown targets Phospho-RPA32 (Ser4, Ser8)

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CHK2 Antibody (antibody)

RRID:AB_513590

This unknown targets Chk2

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Anti-Chk2, phospho (Thr68) Antibody, Unconjugated (antibody)

RRID:AB_331479

This polyclonal targets Chk2, phospho (Thr68)

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ATM Antibody (antibody)

RRID:AB_263415

This unknown targets ATM

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Chk1 Antibody (antibody)

RRID:AB_309459

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Phospho-Chk1 (Ser345) (133D3) Rabbit mAb (antibody)

RRID:AB_331212

This monoclonal targets Chk1, phospho (Ser345)

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H2AX Antibody (antibody)

RRID:AB_203289

This unknown targets H2AX

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