pH dependence of self-splicing by the group IA2 intron in a pre-mRNA derived from the nrdB gene of bacteriophage T4

• Published in: Nucleic acids research 1997-09, Vol.25 (17), p.3543-3549
• Main Author: Sjogren, A.
• Format: Article
• Language: English
• Subjects: Bacteriophage T4 - genetics; Deoxyguanosine - analogs & derivatives; Deoxyguanosine - metabolism; Deoxyguanosine - pharmacology; Esterification; Guanosine - metabolism; Hydrogen-Ion Concentration; Introns; Magnesium - pharmacology; Medicin och hälsovetenskap; Nucleic Acid Conformation; Phage T4; Ribonucleoside Diphosphate Reductase - genetics; RNA Precursors - metabolism; RNA Splicing; RNA, Messenger - metabolism; RNA, Viral - metabolism
• ISSN: 0305-1048; 1362-4962; 1362-4962
• DOI: 10.1093/nar/25.17.3543

The nrdB gene of bacteriophage T4 contains a group IA2 intron. We have investigated the kinetics of self-splicing by a shortened variant of nrdB pre-mRNA in the presence of the co-substrates guanosine and 2′-amino-2′-deoxyguanosine. The pH dependence of the first transesterification step displayed parallel linear correlations for the two different co-substrates up to pH 7, above which the reaction with guanosine levels off to become pH independent. The plot for the 30-fold slower reaction with 2′-aminoguanosine is linear up to pH 8–8.5 and then levels off. The linear correlations with slopes close to unity suggest that a deprotonation event accelerates the transesterification reaction and that a change in rate limiting step occurs at a first order rate constant of ∼1 min−1 (i.e. for our system kcat/Km ≈ 105 M−1 min−1). The pH dependence of observed rate constants in different divalent metal ion mixtures, where the 2′-aminoguanosine-dependent reaction is enhanced 6- and 35-fold compared with that in magnesium, strongly supports this conclusion. This is, to our knowledge, the first report on an intact self-splicing group I intron where use of different co-substrates and divalent metal ions shows that a deprotonation enhances the rate and verifies that the transitions occurring during splicing of group I introns are all part of a common reaction sequence.