Evidence map›Paper›PMID 24045951›Full record

ArticleThe Journal of biological chemistry2013

The Rho family member RhoE interacts with Skp2 and is degraded at the proteasome during cell cycle progression.

Marta Lonjedo, Enric Poch, Enric Mocholí, Marta Hernández-Sánchez, Carmen Ivorra, Thomas F Franke, Rosa M Guasch, Ignacio Pérez-Roger

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

17 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Phosphorylation of Arl4A/D promotes their binding by the HYPK chaperone for their stable recruitment to the plasma membrane.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Regulating Rho GTPases and their regulators.Nature reviews. Molecular cell biology · 2016
    Review
  11. Article
  12. Article
  13. Pathophysiological Functions of Rnd3/RhoE.Comprehensive Physiology · 2015
    Review
  14. Article
  15. Article
  16. Article
  17. 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 3 institutions in 2 countries.

Marta LonjedoFrom the Instituto de Ciencias Biomédicas, Facultad de Ciencias de la Salud, Universidad CEU Cardenal Herrera, 46113-Moncada (Valencia), Spain.
Enric Poch
Enric Mocholí
Marta Hernández-Sánchez
Carmen Ivorra
Thomas F Franke
Rosa M Guasch
Ignacio Pérez-Roger
Universidad Cardenal Herrera CEU · ESCentro de Investigacion Principe Felipe · ESNew York University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RhoE/Rnd3 is an atypical member of the Rho family of small GTPases. In addition to regulating actin cytoskeleton dynamics, RhoE is involved in the regulation of cell proliferation, survival, and metastasis. We examined RhoE expression levels during cell cycle and investigated mechanisms controlling them. We show that RhoE accumulates during G1, in contact-inhibited cells, and when the Akt pathway is inhibited. Conversely, RhoE levels rapidly decrease at the G1/S transition and remain low for most of the cell cycle. We also show that the half-life of RhoE is shorter than that of other Rho proteins and that its expression levels are regulated by proteasomal degradation. The expression patterns of RhoE overlap with that of the cell cycle inhibitor p27. Consistently with an involvement of RhoE in cell cycle regulation, RhoE and p27 levels decrease after overexpression of the F-box protein Skp2. We have identified a region between amino acids 231 and 240 of RhoE as the Skp2-interacting domain and Lys(235) as the substrate for ubiquitylation. Based on our results, we propose a mechanism according to which proteasomal degradation of RhoE by Skp2 regulates its protein levels to control cellular proliferation.

Indexed as

ProteolysisCyclin-Dependent Kinase Inhibitor p21G1 PhaseGene Expression RegulationHeLa CellsHumansProteasome Endopeptidase Complexrho GTP-Binding ProteinsS-Phase Kinase-Associated ProteinsUbiquitinationCDKN1A protein, humanCyclin-Dependent Kinase Inhibitor p21Proteasome Endopeptidase Complexrho GTP-Binding ProteinsRND3 protein, humanS-Phase Kinase-Associated ProteinsAktCell Cyclep27Proteasomal DegradationProteasomeRhoERho GTPasesSkp2Ubiquitylation

Identifiers

PMID24045951
PMCPMC3829402
OpenAlexW2014159972

What OpenQuestion holds

Textmetadata
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.