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Molecular modelling of the GIR1 branching ribozyme gives new insight into evolution of structurally related ribozymes
Author(s) -
Beckert Bertrand,
Nielsen Henrik,
Einvik Christer,
Johansen Steinar D,
Westhof Eric,
Masquida Benoît
Publication year - 2008
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.1038/emboj.2008.4
Subject(s) - ribozyme , biology , mammalian cpeb3 ribozyme , group ii intron , ligase ribozyme , vs ribozyme , rna splicing , hairpin ribozyme , group i catalytic intron , genetics , homing endonuclease , intron , rna , computational biology , gene
Twin‐ribozyme introns contain a branching ribozyme (GIR1) followed by a homing endonuclease (HE) encoding sequence embedded in a peripheral domain of a group I splicing ribozyme (GIR2). GIR1 catalyses the formation of a lariat with 3 nt in the loop, which caps the HE mRNA. GIR1 is structurally related to group I ribozymes raising the question about how two closely related ribozymes can carry out very different reactions. Modelling of GIR1 based on new biochemical and mutational data shows an extended substrate domain containing a GoU pair distinct from the nucleophilic residue that dock onto a catalytic core showing a different topology from that of group I ribozymes. The differences include a core J8/7 region that has been reduced and is complemented by residues from the pre‐lariat fold. These findings provide the basis for an evolutionary mechanism that accounts for the change from group I splicing ribozyme to the branching GIR1 architecture. Such an evolutionary mechanism can be applied to other large RNAs such as the ribonuclease P.