FB2026_03 , released September 17, 2026
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Citation
Vargas, D.Y., Shah, K., Batish, M., Levandoski, M., Sinha, S., Marras, S.A., Schedl, P., Tyagi, S. (2011). Single-molecule imaging of transcriptionally coupled and uncoupled splicing.  Cell 147(5): 1054--1065.
FlyBase ID
FBrf0217264
Publication Type
Research paper
Abstract
Introns are removed from pre-mRNAs during transcription while the pre-mRNA is still tethered to the gene locus via RNA polymerase. However, during alternative splicing, it is important that splicing be deferred until all of the exons and introns involved in the choice have been synthesized. We have developed an in situ RNA imaging method with single-molecule sensitivity to define the intracellular sites of splicing. Using this approach, we found that the normally tight coupling between transcription and splicing is broken in situations where the intron's polypyrimidine tract is sequestered within strong secondary structures. We also found that in two cases of alternative splicing, in which certain exons are skipped due to the activity of the RNA-binding proteins Sxl and PTB, splicing is uncoupled from transcription. This uncoupling occurs only on the perturbed introns, whereas the preceding and succeeding introns are removed cotranscriptionally. PAPERCLIP:
Graphical Abstract
Obtained with permission from Cell Press.
PubMed ID
PubMed Central ID
PMC3245879 (PMC) (EuropePMC)
Related Publication(s)
Note

Gene expression: splicing steps aside to consider its options.
Burgess, 2012, Nat. Rev. Genet. 13(1): 2 [FBrf0218622]

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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Cell
    Title
    Cell
    Publication Year
    1974-
    ISBN/ISSN
    0092-8674
    Data From Reference
    Genes (2)