Contribution of base-pairing interactions between group II intron fragments during trans-splicing in vivo

被引:10
|
作者
Quiroga, Cecilia [1 ]
Kronstad, Lisa [1 ]
Ritlop, Christine [1 ]
Filion, Audrey [1 ]
Cousineau, Benoit [1 ]
机构
[1] McGill Univ, Dept Microbiol & Immunol, Montreal, PQ H3A 2B4, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Ll.LtrB; Lactococcus lactis; LtrA; conjugation; sex factor; LACTOCOCCUS-LACTIS; REVERSE TRANSCRIPTASE/MATURASE; RNA; VERSATILITY; MECHANISM; ELEMENTS; BINDING; SYSTEM; MODEL; SITE;
D O I
10.1261/rna.028886.111
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Group II introns are mobile genetic elements that self-splice from pre-mRNA transcripts. Some fragmented group II introns found in chloroplastic and mitochondrial genomes are able to assemble and splice in trans. The Ll.LtrB group II intron from the Gram-positive bacterium Lactococcus lactis was shown to splice in trans when fragmented at various locations throughout its structure. Here we used Ll.LtrB to assess the contribution of base-pairing interactions between intron fragments during trans-splicing in vivo. By comparing closely located fragmentation sites, we show that Ll. LtrB trans-splices more efficiently when base-pairing interactions can occur between the two intron fragments. Disruptions and stepwise restorations of specific base-pairing interactions between intron fragments resulted respectively in significant reductions and recoveries of the Ll. LtrB trans-splicing efficiency. Finally, although we confirm that LtrA is an important co-factor for trans-splicing, its overexpression cannot compensate for the reduction in trans-splicing efficiency when the potential base-pairing interactions between intron fragments are disrupted. These findings demonstrate the important contribution of base-pairing interactions for the assembly of group II intron fragments during trans-splicing and rationalizes why such interactions were evolutionarily conserved in natural trans-splicing group II introns.
引用
收藏
页码:2212 / 2221
页数:10
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