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A protein encoded by a group I intron in Aspergillus nidulans directly assists RNA splicing and is a DNA endonuclease
Author(s) -
Yugong Ho,
Sea-Jin Kim,
Richard B. Waring
Publication year - 1997
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.94.17.8994
Subject(s) - intron , group ii intron , rna splicing , minor spliceosome , biology , group i catalytic intron , genetics , protein splicing , aspergillus nidulans , rna , retrotransposon , splicing factor , minigene , exonic splicing enhancer , gene , genome , transposable element , mutant
Some group I introns self-splice in vitro, but almost all are thought to be assisted by proteins in vivo. Mutational analysis has shown that the splicing of certain group I introns depends upon a maturase protein encoded by the intron itself. However the effect of a protein on splicing can be indirect. We now provide evidence that a mitochondrial intron-encoded protein from Aspergillus nidulans directly facilitates splicing in vitro. This demonstrates that a maturase is an RNA splicing protein. The protein-assisted reaction is as fast as that of any other known group I intron. Interestingly the protein is also a DNA endonuclease, an activity required for intron mobilization. Mobile elements frequently encode proteins that promote their propagation. Intron-encoded proteins that also assist RNA splicing would facilitate both the transposition and horizontal transmission of introns.

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