Evidence map›Paper›PMID 28374191›Full record

ReviewHuman genetics2017

Alternative splicing: the pledge, the turn, and the prestige : The key role of alternative splicing in human biological systems.

L M Gallego-Paez, M C Bordone, A C Leote, N Saraiva-Agostinho, M Ascensão-Ferreira, N L Barbosa-Morais

Open access · hybridAbstract readReview
In one paragraph

Review in Human genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

77 citing papers in PubMed, 133 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. DecipheringGenes · 2026
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

17 more citing papers are in PubMed but not listed here.

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

6 authors at 1 institution in 2 countries.

L M Gallego-PaezInstituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Lisboa, Portugal.
M C BordoneInstituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Lisboa, Portugal.
A C LeoteInstituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Lisboa, Portugal.
N Saraiva-AgostinhoInstituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Lisboa, Portugal.
M Ascensão-FerreiraInstituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Lisboa, Portugal.
N L Barbosa-MoraisInstituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Lisboa, Portugal. nmorais@medicina.ulisboa.pt.ORCID 0000-0002-1215-0538
University of Lisbon · PT

Funding

European Molecular Biology Organization Installation Grant (3057)Fundação AstraZeneca Innovate Competition AwardFundação para a Ciência e a Tecnologia Investigador FCT Starting Grant (IF/00595/2014)Fundação para a Ciência e a Tecnologia PhD fellowship (PD/BD/105854/2014)Fundação para a Ciência e a Tecnologia PhD fellowship (PD/BD/128283/2017)iMM/FCT/MEC/FEDER IMM/BPD/45-2016,LISBOA-01-0145-FEDER-007391Instituto de Medicina Molecular Start-up fundsUnited Nations Educational, Scientific and Cultural Organization Women in Science Program (ERI/NCS/FLP/CDC.13.94)
6 · The paper itself

Abstract

Alternative pre-mRNA splicing is a tightly controlled process conducted by the spliceosome, with the assistance of several regulators, resulting in the expression of different transcript isoforms from the same gene and increasing both transcriptome and proteome complexity. The differences between alternative isoforms may be subtle but enough to change the function or localization of the translated proteins. A fine control of the isoform balance is, therefore, needed throughout developmental stages and adult tissues or physiological conditions and it does not come as a surprise that several diseases are caused by its deregulation. In this review, we aim to bring the splicing machinery on stage and raise the curtain on its mechanisms and regulation throughout several systems and tissues of the human body, from neurodevelopment to the interactions with the human microbiome. We discuss, on one hand, the essential role of alternative splicing in assuring tissue function, diversity, and swiftness of response in these systems or tissues, and on the other hand, what goes wrong when its regulatory mechanisms fail. We also focus on the possibilities that splicing modulation therapies open for the future of personalized medicine, along with the leading techniques in this field. The final act of the spliceosome, however, is yet to be fully revealed, as more knowledge is needed regarding the complex regulatory network that coordinates alternative splicing and how its dysfunction leads to disease.

Indexed as

Alternative SplicingHumansMicrobiotaRNA, MessengerRNA, MessengerAlternative SpliceDuchenne Muscular DystrophyRound SpermatidSpinal Muscular AtrophySplice Factor

Identifiers

PMID28374191
PMCPMC5602094
OpenAlexW2605134565

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.