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Diverse mechanisms for spliceosome-mediated 3′ end processing of telomerase RNA

Author

Listed:
  • Ram Kannan

    (Stowers Institute for Medical Research
    University of Kansas Medical Center
    Present address: Memorial Sloan Kettering Cancer Center, 417 E 68th Street, New York, New York 10065, USA)

  • Rachel M. Helston

    (Stowers Institute for Medical Research)

  • Richard O. Dannebaum

    (Stowers Institute for Medical Research)

  • Peter Baumann

    (Stowers Institute for Medical Research
    University of Kansas Medical Center
    Howard Hughes Medical Institute)

Abstract

The 3′ end of Schizosaccharomyces pombe telomerase RNA (SpTER1) is generated by spliceosomal cleavage, a reaction that corresponds to the first step of splicing. The observation that the spliceosome functions in 3′ end processing raised questions about the evolutionary origin and conservation of this mechanism. We now present data in support of spliceosomes generating 3′ ends of telomerase RNAs in other fungi. Strikingly, the mechanistic basis for restricting spliceosomal splicing to the first transesterification reaction differs substantially among species. Unlike S. pombe, two other fission yeasts rely on hyperstabilization of the U6 snRNA—5′ splice site interaction to impede the 2nd step of splicing. In contrast, a non-canonical 5′ splice site blocks the second transesterification reaction in Aspergillus species. These results demonstrate a conserved role for spliceosomes functioning in 3′ end processing. Divergent mechanisms of uncoupling the two steps of splicing argue for multiple origins of this pathway.

Suggested Citation

  • Ram Kannan & Rachel M. Helston & Richard O. Dannebaum & Peter Baumann, 2015. "Diverse mechanisms for spliceosome-mediated 3′ end processing of telomerase RNA," Nature Communications, Nature, vol. 6(1), pages 1-8, May.
  • Handle: RePEc:nat:natcom:v:6:y:2015:i:1:d:10.1038_ncomms7104
    DOI: 10.1038/ncomms7104
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