Group II intron splicing in vivo by first-step hydrolysis
Mircea Podar,
Vi T. Chu,
Anna Marie Pyle and
Philip S. Perlman ()
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Mircea Podar: University of Texas Southwestern Medical Center
Vi T. Chu: Columbia University College of Physicians and Surgeons
Anna Marie Pyle: Columbia University College of Physicians and Surgeons
Philip S. Perlman: University of Texas Southwestern Medical Center
Nature, 1998, vol. 391, issue 6670, 915-918
Abstract:
Abstract Group I, group II and spliceosomal introns splice by two sequential transesterification reactions1. For both spliceosomal and group II introns, the first-step reaction occurs by nucleophilic attack on the 5′ splice junction by the 2′ hydroxyl of an internal adenosine, forming a 2′–5′ phosphodiester branch in the intron. The second reaction joins the two exons with a 3′–5′ phosphodiester bond and releases intron lariat. In vitro, group II introns can self-splice by an efficient alternative pathway in which the first-step reaction occurs by hydrolysis. The resulting linear splicing intermediate participates in normal second-step reactions, forming spliced exon and linear intron RNAs2,3. Here we show that the group II intron first-step hydrolysis reaction occurs in vivo in place of transesterification in the mitochondria of yeast strains containing branch-site mutations. As expected, the mutations block branching, but surprisingly still allow accurate splicing. This hydrolysis pathway may have been a step in the evolution of splicing mechanisms.
Date: 1998
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Persistent link: https://EconPapers.repec.org/RePEc:nat:nature:v:391:y:1998:i:6670:d:10.1038_36142
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DOI: 10.1038/36142
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