Evidence map›Paper›PMID 18458335›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2008

Cis- and trans-splicing of mRNAs mediated by tRNA sequences in eukaryotic cells.

Gianfranco Di Segni, Serena Gastaldi, Glauco P Tocchini-Valentini

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.0field-weighted citation impact, top 26% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. AtFusionDB: a database of fusion transcripts in Arabidopsis thaliana.Database : the journal of biological databases and curation · 2019
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Yeast pheromone receptor genes STE2 and STE3 are differently regulated at the transcription and polyadenylation level.Proceedings of the National Academy of Sciences of the United States of America · 2011
    Article
  15. tRNA biology charges to the front.Genes & development · 2010
    Review
  16. Article
  17. Article
  18. Long-distance splicing.Proceedings of the National Academy of Sciences of the United States of America · 2008
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 2 countries.

Gianfranco Di SegniIstituto di Biologia Cellulare, Consiglio Nazionale delle Ricerche, Via Ramarini 32, 00015 Monterotondo (Rome), Italy.
Serena Gastaldi
Glauco P Tocchini-Valentini
University of Chicago · USInstitute of Cell Biology and Neurobiology · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The formation of chimeric mRNAs is a strategy used by human cells to increase the complexity of their proteome, as revealed by the ENCODE project. Here, we use Saccharomyces cerevisiae to show a way by which trans-spliced mRNAs can be generated. We demonstrate that a pretRNA inserted into a premRNA context directs the splicing reaction precisely to the sites of the tRNA intron. A suppressor pretRNA gene was inserted, in cis, into the sequence encoding the third cytoplasmic loop of the Ste2 or Ste3 G protein-coupled receptor. The hybrid RNAs are spliced at the specific pretRNA splicing sites, releasing both functional tRNAs that suppress nonsense mutations and translatable mRNAs that activate the signal transduction pathway. The RNA molecules extracted from yeast cells were amplified by RT-PCR, and their sequences were determined, confirming the identity of the splice junctions. We then constructed two fusions between the premRNA sequence (STE2 or STE3) and the 5'- or 3'-pretRNA half, so that the two hybrid RNAs can associate with each other, in trans, through their tRNA halves. Splicing occurs at the predicted pretRNA sites, producing a chimeric STE3-STE2 receptor mRNA. RNA trans-splicing mediated by tRNA sequences, therefore, is a mechanism capable of producing new kinds of RNAs, which could code for novel proteins.

Indexed as

Base SequenceEukaryotic CellsGene Expression Regulation, FungalGenes, Mating Type, FungalMolecular Sequence DataNucleic Acid ConformationNucleic Acid HeteroduplexesProtein BiosynthesisReverse Transcriptase Polymerase Chain ReactionRNA, MessengerRNA PrecursorsRNA Splice SitesRNA, TransferSaccharomyces cerevisiaeSequence DeletionSignal TransductionNucleic Acid HeteroduplexesRNA, MessengerRNA PrecursorsRNA Splice SitesRNA, Transfer

Identifiers

PMID18458335
PMCPMC2383978
OpenAlexW1977678165

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.