Group I and group II introns are dynamic genetic elements that splice by different self-catalyzed RNA-based mechanisms. Many are also capable of insertion into DNA through distinctive mobility pathways. For each class of intron, mobility characteristically takes the form of homing, whereby the intron transfers to an intronless DNA allele via a break created by an intron-encoded endonuclease. For group I intron homing, recombination events are strictly DNA-based, whereas group II intron homing, also termed retrohoming, involves RNA at levels of both the template and cleavage enzyme for mobility. The overall goal of this work is to study in bacteria the DNA-based and RNA-based intron rearrangements of these phylogenetically diverse elements. During the past funding period the PI made progress in understanding the role of DNA exonucleases in group I intron mobility, and in demonstrating illegitimate double-strand-break repair in intron acquisition, suggesting that such a mechanism might account for intron invasion of ectopic sites. In independent studies, the PI defined the domain structure and function of StpA, an RNA chaperone that promotes splicing of group I introns. The PI also determined the mode of action of DsrA, an E. coli regulatory RNA. Finally, in major breakthoughs for the field, the PI established a group II intron as the first functional retrotransposon in prokaryotes demonstrating both RNA-based retrohoming and retrotransposition to ectopic sites. In addition to the innate mechanistic importance of these results, the invasiveness of group II introns and their similarities to human retrotransposons and spliceosomal introns have great evolutionary and health significance. For the next funding period the PI proposes to demonstrate transposition of group I introns. Additionally, the PI will extend her analysis of the RNA chaperone function of StpA and further define its structure and global regulatory activity. The PI will also build on her mechanistic studies and define accessory molecules required for group II intron retrohoming and retrotransposition. Finally, the PI will ask evolutionary questions relating to group II intron dispersal, the relationship of group II introns to spliceosomal introns of eukaryotes, and the possible role of group II introns in affecting horizontal gene transfer. Thus, by combining the approaches of genetics, biochemistry, and structural analysis, the PI proposes to advance our understanding of intron-related nucleic acid dynamics and intron evolution.
| Qu, Guosheng; Piazza, Carol Lyn; Smith, Dorie et al. (2018) Group II intron inhibits conjugative relaxase expression in bacteria by mRNA targeting. Elife 7: |
| Lennon, Christopher W; Stanger, Matthew; Banavali, Nilesh K et al. (2018) Conditional Protein Splicing Switch in Hyperthermophiles through an Intein-Extein Partnership. MBio 9: |
| Kelley, Danielle S; Lennon, Christopher W; Li, Zhong et al. (2018) Mycobacterial DnaB helicase intein as oxidative stress sensor. Nat Commun 9:4363 |
| Belfort, Marlene (2017) Mobile self-splicing introns and inteins as environmental sensors. Curr Opin Microbiol 38:51-58 |
| Novikova, Olga; Belfort, Marlene (2017) Mobile Group II Introns as Ancestral Eukaryotic Elements. Trends Genet 33:773-783 |
| Qu, Guosheng; Kaushal, Prem Singh; Wang, Jia et al. (2016) Structure of a group II intron in complex with its reverse transcriptase. Nat Struct Mol Biol 23:549-57 |
| Novikova, Olga; Jayachandran, Pradeepa; Kelley, Danielle S et al. (2016) Intein Clustering Suggests Functional Importance in Different Domains of Life. Mol Biol Evol 33:783-99 |
| Lennon, Christopher W; Stanger, Matthew; Belfort, Marlene (2016) Protein splicing of a recombinase intein induced by ssDNA and DNA damage. Genes Dev 30:2663-2668 |
| Chan, Hon; Pearson, C Seth; Green, Cathleen M et al. (2016) Exploring Intein Inhibition by Platinum Compounds as an Antimicrobial Strategy. J Biol Chem 291:22661-22670 |
| Tsai, Chen-Hsun; Liao, Rick; Chou, Brendan et al. (2015) Genome-wide analyses in bacteria show small-RNA enrichment for long and conserved intergenic regions. J Bacteriol 197:40-50 |
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