Evidence map›Paper›PMID 18280241›Full record

ArticleMolecular cell2008

Ran-binding protein 3 phosphorylation links the Ras and PI3-kinase pathways to nucleocytoplasmic transport.

Sang-Oh Yoon, Sejeong Shin, Yuzhen Liu, Bryan A Ballif, Michele S Woo, Steven P Gygi, John Blenis

Abstract read
In one paragraph

Article in Molecular cell, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing 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

50 citing papers in PubMed.

  1. Review
  2. Ran GTPase and Its Importance in Cellular Signaling and Malignant Phenotype.International journal of molecular sciences · 2023
    Review
  3. Article
  4. Multi-omic comparative analysis of COVID-19 and bacterial sepsis-induced ARDS.medRxiv : the preprint server for health sciences · 2022
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Regulation of nuclear mTORC1.Molecular & cellular oncology · 2021
    Article
  10. Article
  11. Ran GTPase: A Key Player in Tumor Progression and Metastasis.Frontiers in cell and developmental biology · 2020
    Review
  12. Article
  13. Intracellular CaCell stem cell · 2019
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Sang-Oh YoonDepartment of Cell Biology, Harvard Medical School, 240 Longwood Avenue, Boston, MA 02115, USA.
Sejeong Shin
Yuzhen Liu
Bryan A Ballif
Michele S Woo
Steven P Gygi
John Blenis

Funding

SIGNAL TRANSDUCTION TO PP70 S6KR01GM051405 · NIGMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI BLENIS, JOHN · 1995 to 2023
$14.0M
Mitogenic and Oncogenic Regulation of ERK/RSK SignalingR37CA046595 · NCI · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI BLENIS, JOHN · 2003 to 2012
$6.4M
New Technologies for Quantitative Phosphorylation AnalysisR01HG003456 · NHGRI · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI GYGI, STEVEN P · 2005 to 2011
$2.7M
NCI NIH HHS R37 CA046595NCI NIH HHS R37 CA46595NHGRI NIH HHS HG3456NHGRI NIH HHS R01 HG003456NIGMS NIH HHS R01 GM051405NIGMS NIH HHS R01 GM5105
6 · The paper itself

Abstract

The major participants of the Ras/ERK and PI3-kinase (PI3K) pathways are well characterized. The cellular response to activation of these pathways, however, can vary dramatically. How differences in signal strength, timing, spatial location, and cellular context promote specific cell-fate decisions remains unclear. Nuclear transport processes can have a major impact on the determination of cell fate; however, little is known regarding how nuclear transport is regulated by or regulates these pathways. Here we show that RSK and Akt, which are activated downstream of Ras/ERK and PI3K, respectively, modulate the Ran gradient and nuclear transport by interacting with, phosphorylating, and regulating Ran-binding protein 3 (RanBP3) function. Our findings highlight an important link between two major cell-fate determinants: nuclear transport and the Ras/ERK/RSK and PI3K/Akt signaling pathways.

Indexed as

Active Transport, Cell NucleusCell NucleusEnzyme ActivationMitogen-Activated Protein KinasesNuclear ProteinsNucleocytoplasmic Transport ProteinsPhosphatidylinositol 3-KinasesPhosphorylationProto-Oncogene Proteins c-aktras ProteinsRibosomal Protein S6 Kinases, 90-kDaSignal TransductionSubstrate SpecificityMitogen-Activated Protein KinasesNuclear ProteinsNucleocytoplasmic Transport ProteinsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktRANBP3 protein, humanras ProteinsRibosomal Protein S6 Kinases, 90-kDa

Identifiers

PMID18280241
PMCPMC2266693

What OpenQuestion holds

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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.