Evidence map›Paper›PMID 28733330›Full record

ArticleThe Biochemical journal2017

The helicase, DDX3X, interacts with poly(A)-binding protein 1 (PABP1) and caprin-1 at the leading edge of migrating fibroblasts and is required for efficient cell spreading.

Alice C Copsey, Simon Cooper, Robert Parker, Ella Lineham, Cuzack Lapworth, Deema Jallad, Steve Sweet, Simon J Morley

Open access · hybridAbstract read
In one paragraph

Article in The Biochemical journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

19 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. RNA binding proteins in cardiovascular development and disease.Current topics in developmental biology · 2024
    Article
  5. mCancer letters · 2023
    Article
  6. Article
  7. Review
  8. Review
  9. The human DEAD-box helicase DDX3X as a regulator of mRNA translation.Frontiers in cell and developmental biology · 2022
    Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Proteomic Analysis of Quercetin-Treated K562 Cells.International journal of molecular sciences · 2019
    Article
  17. Article
  18. Role of caprin-1 in carcinogenesis.Oncology letters · 2019
    Review
  19. Review
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

8 authors at 2 institutions in 2 countries.

Alice C CopseyDepartment of Biochemistry, School of Life Sciences, University of Sussex, Brighton BN1 6SE, U.K.
Simon CooperDepartment of Biochemistry, School of Life Sciences, University of Sussex, Brighton BN1 6SE, U.K.
Robert ParkerFaculty of Medicine, National Heart & Lung Institute, St Mary's Campus, Imperial College London, London W2 1NY, U.K.
Ella LinehamDepartment of Biochemistry, School of Life Sciences, University of Sussex, Brighton BN1 6SE, U.K.
Cuzack LapworthDepartment of Biochemistry, School of Life Sciences, University of Sussex, Brighton BN1 6SE, U.K.
Deema JalladDepartment of Biochemistry, School of Life Sciences, University of Sussex, Brighton BN1 6SE, U.K.
Steve SweetGenome Damage and Stability Centre, School of Life Sciences, University of Sussex, Brighton BN1 9RQ, U.K.
Simon J MorleyDepartment of Biochemistry, School of Life Sciences, University of Sussex, Brighton BN1 6SE, U.K. s.j.morley@sussex.ac.uk.
University of Sussex · GBLung Institute · US

Funding

Biotechnology and Biological Sciences Research Council BB/H018956/1Biotechnology and Biological Sciences Research Council BB/L018209/1Medical Research Council G1100257
6 · The paper itself

Abstract

DDX3X, a helicase, can interact directly with mRNA and translation initiation factors, regulating the selective translation of mRNAs that contain a structured 5' untranslated region. This activity modulates the expression of mRNAs controlling cell cycle progression and mRNAs regulating actin dynamics, contributing to cell adhesion and motility. Previously, we have shown that ribosomes and translation initiation factors localise to the leading edge of migrating fibroblasts in loci enriched with actively translating ribosomes, thereby promoting steady-state levels of ArpC2 and Rac1 proteins at the leading edge of cells during spreading. As DDX3X can regulate Rac1 levels, cell motility and metastasis, we have examined DDX3X protein interactions and localisation using many complementary approaches. We now show that DDX3X can physically interact and co-localise with poly(A)-binding protein 1 and caprin-1 at the leading edge of spreading cells. Furthermore, as depletion of DDX3X leads to decreased cell motility, this provides a functional link between DDX3X, caprin-1 and initiation factors at the leading edge of migrating cells to promote cell migration and spreading.

Indexed as

Blotting, WesternCell Cycle ProteinsCell LineCell MovementChromatography, AffinityCRISPR-Cas SystemsDEAD-box RNA HelicasesFluorescent DyesHumansImmunoprecipitationLungMicroscopy, ConfocalMicroscopy, FluorescencePeptide MappingPoly(A)-Binding Protein IProtein TransportCAPRIN1 protein, humanCell Cycle ProteinsDDX3X protein, humanDEAD-box RNA HelicasesFluorescent DyesPoly(A)-Binding Protein IRNA, Messengercell migrationDDX3Xtranslationtranslation factors

Identifiers

PMID28733330
PMCPMC5577505
OpenAlexW2738586477

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.