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Toward predicting self-splicing and protein-facilitated splicing of group I introns
Open accessAbstract
In the current era of massive discoveries of noncoding RNAs within genomes, being able to infer a function from a nucleotide sequence is of paramount interest. Although studies of individual group I introns have identified self-splicing and nonself-splicing examples, there is no overall understanding of the prevalence of self-splicing or the factors that determine it among the >2300 group I introns sequenced to date. Here, the self-splicing activities of 12 group I introns from various organisms were assayed under six reaction conditions that had been shown previously to promote RNA catalysis for different RNAs. Besides revealing that assessing self-splicing under only one condition can be misleading, this survey emphasizes that in vitro self-splicing efficiency is correlated with the GC content of the intron (>35% GC was generally conductive to self-splicing), and with the ability of the introns to form particular tertiary interactions. Addition of the Neurospora crassa CYT-18 protein activated splicing of two nonself-splicing introns, but inhibited the second step of self-splicing for two others. Together, correlations between sequence, predicted structure and splicing begin to establish rules that should facilitate our ability to predict the self-splicing activity of any group I intron from its sequence.
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Native group I introns have an average intervening region between the 5′ and 3′ splice sites of 300-500 nucleotides.
“Indeed, the intervening region between the 5′ and 3′ splice sites of native group I introns is on average 300–500 nucleotides long22, while the intervening region of the engineered RNA that we constructed was two to four-fold longer.”
From Engineering circular RNA for potent and stable translation in eukaryotic cells (2018) · cites this paper as [22]
The Results section reports that 12 group I introns tested were 183–421 nucleotides long, and Intron selection gives a range of 183–496 nucleotides for introns requested. Neither passage establishes a 300–500-nucleotide average for native group I introns generally. (LLM, conf=0.82)
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Metadata
- Authors
- Vicens, Q., Paukstelis, P. J., Westhof, E., Lambowitz, A. M., & Cech, T. R.
- Affiliations
- Howard Hughes Medical Institute (US)
- The University of Texas at Austin (US)
- Venue
- RNA
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2008-09-03
- Volume
- 14
- Issue
- 10
- Pages
- 2013-2029
- ISSN
- 1355-8382 (ISSN-L)
- 1469-9001
- PMC
- PMC2553746
- OpenAlex
- W2110018116
- Cited by
- 49
- References
- 86
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 5 · 2023: 3 · 2022: 2 · 2021: 2 · 2018: 5 · 2017: 2 · 2014: 4 · 2013: 4 · 2012: 4
- FWCI
- 1.92
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- RNA (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- CU Scholar (University of Colorado Boulder) (submittedVersion)
- HAL (submittedVersion)
- HighWire Press Open Archive (submittedVersion)
- Funders
- Howard Hughes Medical Institute
- National Institutes of Health (GM037951)
- National Institute of General Medical Sciences (R37GM037951, R01GM037951, GM037951)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Research and Splicing
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA regulation and disease
- Keywords
- group I introns, self-splicing, GC content, tertiary interactions, Neurospora crassa, RNA catalysis, sequence-structure-function relationships
- MeSH terms
- Base Composition, Base Sequence, Catalysis, Introns, Neurospora crassa, Nucleic Acid Conformation, RNA Splicing, RNA, Messenger, Tyrosine-tRNA Ligase, RNA, Catalytic
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