Evidence map›Paper›PMID 21605368›Full record

ArticleBMC molecular biology2011

Exon sequence requirements for excision in vivo of the bacterial group II intron RmInt1.

Antonio Barrientos-Durán, Isabel Chillón, Francisco Martínez-Abarca, Nicolás Toro

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Article in BMC molecular biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

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8citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Contribution of Mobile Group II Introns toFrontiers in microbiology · 2018
    Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Visualizing the ai5γ group IIB intron.Nucleic acids research · 2014
    Article
  7. Article
  8. Article
4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Antonio Barrientos-DuránGrupo de Ecología Genética, Estación Experimental del Zaidín, Consejo Superior de Investigaciones Científicas (CSIC), C/Profesor Albareda 1, 18008 Granada, Spain.
Isabel Chillón
Francisco Martínez-Abarca
Nicolás Toro

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGroup II intron splicing proceeds through two sequential transesterification reactions in which the 5' and 3'-exons are joined together and the lariat intron is released. The intron-encoded protein (IEP) assists the splicing of the intron in vivo and remains bound to the excised intron lariat RNA in a ribonucleoprotein particle (RNP) that promotes intron mobility. Exon recognition occurs through base-pairing interactions between two guide sequences on the ribozyme domain dI known as EBS1 and EBS2 and two stretches of sequence known as IBS1 and IBS2 on the 5' exon, whereas the 3' exon is recognized through interaction with the sequence immediately upstream from EBS1 [(δ-δ' interaction (subgroup IIA)] or with a nucleotide [(EBS3-IBS3 interaction (subgroup IIB and IIC))] located in the coordination-loop of dI. The δ nucleotide is involved in base pairing with another intron residue (δ') in subgroup IIB introns and this interaction facilitates base pairing between the 5' exon and the intron.

resultsIn this study, we investigated nucleotide requirements in the distal 5'- and 3' exon regions, EBS-IBS interactions and δ-δ' pairing for excision of the group IIB intron RmInt1 in vivo. We found that the EBS1-IBS1 interaction was required and sufficient for RmInt1 excision. In addition, we provide evidence for the occurrence of canonical δ-δ' pairing and its importance for the intron excision in vivo.

conclusionsThe excision in vivo of the RmInt1 intron is a favored process, with very few constraints for sequence recognition in both the 5' and 3'-exons. Our results contribute to understand how group II introns spread in nature, and might facilitate the use of RmInt1 in gene targeting.

Indexed as

ExonsBase PairingBase SequenceIntronsMutationNucleic Acid ConformationRNA, BacterialRNA, CatalyticRNA SplicingSinorhizobium melilotiRNA, BacterialRNA, Catalytic

Identifiers

PMID21605368
PMCPMC3123198

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.