Autocatalytic RNA cleavage in the human β-globin pre-mRNA promotes transcription termination

Alexandre Teixeira, Abdessamad Tahiri-Alaoui, Steve West, Benjamin Thomas, Aroul Ramadass, Igor Martianov, Mick Dye, William James, Nick J. Proudfoot and Alexandre Akoulitchev ()
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Alexandre Teixeira: University of Oxford
Abdessamad Tahiri-Alaoui: University of Oxford
Steve West: University of Oxford
Benjamin Thomas: University of Oxford
Aroul Ramadass: The Wellcome Trust Sanger Institute
Igor Martianov: University of Oxford
Mick Dye: University of Oxford
William James: University of Oxford
Nick J. Proudfoot: University of Oxford
Alexandre Akoulitchev: University of Oxford

Nature, 2004, vol. 432, issue 7016, 526-530

Abstract: Abstract New evidence indicates that termination of transcription is an important regulatory step, closely related to transcriptional interference1 and even transcriptional initiation2. However, how this occurs is poorly understood. Recently, in vivo analysis of transcriptional termination for the human β-globin gene revealed a new phenomenon—co-transcriptional cleavage (CoTC)3. This primary cleavage event within β-globin pre-messenger RNA, downstream of the poly(A) site, is critical for efficient transcriptional termination by RNA polymerase II3. Here we show that the CoTC process in the human β-globin gene involves an RNA self-cleaving activity. We characterize the autocatalytic core of the CoTC ribozyme and show its functional role in efficient termination in vivo. The identified core CoTC is highly conserved in the 3′ flanking regions of other primate β-globin genes. Functionally, it resembles the 3′ processive, self-cleaving ribozymes described for the protein-encoding genes from the myxomycetes Didymium iridis and Physarum polycephalum, indicating evolutionary conservation of this molecular process. We predict that regulated autocatalytic cleavage elements within pre-mRNAs may be a general phenomenon and that functionally it may provide the entry point for exonucleases involved in mRNA maturation, turnover and, in particular, transcriptional termination.

Date: 2004
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DOI: 10.1038/nature03032

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