Evidence map›Paper›PMID 18838389›Full record

ArticleNucleic acids research2008

Low conservation and species-specific evolution of alternative splicing in humans and mice: comparative genomics analysis using well-annotated full-length cDNAs.

Jun-Ichi Takeda, Yutaka Suzuki, Ryuichi Sakate, Yoshiharu Sato, Masahide Seki, Takuma Irie, Nono Takeuchi, Takuya Ueda, Mitsuteru Nakao, Sumio Sugano and 2 more

Abstract readComparative Study
In one paragraph

Article in Nucleic acids research, 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
–field-weighted citation impact
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.

  1. Article
  2. Review
  3. Detection of orthologous exons and isoforms using EGIO.Bioinformatics (Oxford, England) · 2022
    Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Architecture and metamorphosis.Topics in current chemistry · 2014
    Review
  10. Article
  11. Review
  12. When orthologs diverge between human and mouse.Briefings in bioinformatics · 2011
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Jun-Ichi TakedaIntegrated Database and Systems Biology Team, Biomedicinal Information Research Center, National Institute of Advanced Industrial Science and Technology, AIST Bio-IT Research Building, Aomi 2-42, Koto-ku, Tokyo, Japan.
Yutaka Suzuki
Ryuichi Sakate
Yoshiharu Sato
Masahide Seki
Takuma Irie
Nono Takeuchi
Takuya Ueda
Mitsuteru Nakao
Sumio Sugano
Takashi Gojobori
Tadashi Imanishi

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Using full-length cDNA sequences, we compared alternative splicing (AS) in humans and mice. The alignment of the human and mouse genomes showed that 86% of 199 426 total exons in human AS variants were conserved in the mouse genome. Of the 20 392 total human AS variants, however, 59% consisted of all conserved exons. Comparing AS patterns between human and mouse transcripts revealed that only 431 transcripts from 189 loci were perfectly conserved AS variants. To exclude the possibility that the full-length human cDNAs used in the present study, especially those with retained introns, were cloning artefacts or prematurely spliced transcripts, we experimentally validated 34 such cases. Our results indicate that even retained-intron type transcripts are typically expressed in a highly controlled manner and interact with translating ribosomes. We found non-conserved AS exons to be predominantly outside the coding sequences (CDSs). This suggests that non-conserved exons in the CDSs of transcripts cause functional constraint. These findings should enhance our understanding of the relationship between AS and species specificity of human genes.

Indexed as

Alternative SplicingEvolution, MolecularAmino Acyl-tRNA SynthetasesAnimalsBase SequenceConserved SequenceData Interpretation, StatisticalDNA, ComplementaryExonsGenomicsHumansIntronsMicePhosphatidylinositol 3-KinasesRNA, MessengerSpecies SpecificityAmino Acyl-tRNA Synthetasescysteinyl-tRNA synthetaseDNA, ComplementaryPhosphatidylinositol 3-KinasesRNA, Messenger

Identifiers

PMID18838389
PMCPMC2582632

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Registered trials

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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.