Evidence map›Paper›PMID 30683695›Full record

ReviewThe Journal of biological chemistry2019

Polyadenylation and nuclear export of mRNAs.

Murray Stewart

Registry-linked trialAbstract readReview
In one paragraph

Review in The Journal of biological chemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06731790 (Role of the Nuclear Pore Component RANBP2 in Inflammatory Responses to Viral Infections), which is not on this map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing 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.

NCT06731790 nacompletednot on this mapstarted 2025, after this paper: background citation

Role of the Nuclear Pore Component RANBP2 in Inflammatory Responses to Viral Infections

TypeinterventionalSponsorUniversity Hospital, MontpellierRan2025 to 2025Enrolled35ConditionsRare Genetic Disease, Acute Necrotizing EncephalopathyArmsBlood sampling for inflammatory phenotype analysis, Blood sampling for genetic analysis
3 · Its place in the literature

Who cites it

73 citing papers in PubMed.

  1. Review
  2. Review
  3. Structure, function and assembly of nuclear pore complexes.Nature reviews. Molecular cell biology · 2026
    Review
  4. Review
  5. Viral interference of nucleocytoplasmic transport.The Journal of biological chemistry · 2025
    Review
  6. RNAMolecular therapy. Nucleic acids · 2025
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. RNA-binding proteins in bone pathophysiology.Frontiers in cell and developmental biology · 2024
    Review
  19. Review
  20. Review

13 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

1 author.

Murray StewartFrom the MRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge Biomedical Campus, Cambridge CB2 0QH, United Kingdom ms@mrc-lmb.cam.ac.uk.

Funding

Medical Research Council MC-A025-5PL41Medical Research Council MC_U105178939Medical Research Council MC_UP_1201/6
6 · The paper itself

Abstract

In eukaryotes, the separation of translation from transcription by the nuclear envelope enables mRNA modifications such as capping, splicing, and polyadenylation. These modifications are mediated by a spectrum of ribonuclear proteins that associate with preRNA transcripts, coordinating the different steps and coupling them to nuclear export, ensuring that only mature transcripts reach the cytoplasmic translation machinery. Although the components of this machinery have been identified and considerable functional insight has been achieved, a number of questions remain outstanding about mRNA nuclear export and how it is integrated into the nuclear phase of the gene expression pathway. Nuclear export factors mediate mRNA transit through nuclear pores to the cytoplasm, after which these factors are removed from the mRNA, preventing transcripts from returning to the nucleus. However, as outlined in this review, several aspects of the mechanism by which transport factor binding and release are mediated remain unclear, as are the roles of accessory nuclear components in these processes. Moreover, the mechanisms by which completion of mRNA splicing and polyadenylation are recognized, together with how they are coordinated with nuclear export, also remain only partially characterized. One attractive hypothesis is that dissociating poly(A) polymerase from the cleavage and polyadenylation machinery could signal completion of mRNA maturation and thereby provide a mechanism for initiating nuclear export. The impressive array of genetic, molecular, cellular, and structural data that has been generated about these systems now provides many of the tools needed to define the precise mechanisms involved in these processes and how they are integrated.

Indexed as

PolyadenylationRNA TransportActive Transport, Cell NucleusAnimalsCell NucleusHumansRNA, MessengerRNA SplicingRNA, Messengergene expression pathwaynuclear porenuclear posttranscriptional modificationnuclear transportpolyadenylationribonuclear protein (RNP)RNA binding proteinRNA helicaseRNA splicingspliceosome

Identifiers

PMID30683695
PMCPMC6398137

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Registered trials

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.