Evidence map›Paper›PMID 11027288›Full record

ArticleMolecular and cellular biology2000

The CUL1 C-terminal sequence and ROC1 are required for efficient nuclear accumulation, NEDD8 modification, and ubiquitin ligase activity of CUL1.

M Furukawa, Y Zhang, J McCarville, T Ohta, Y Xiong

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

70 citing papers in PubMed, 125 citations in OpenAlex.

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  19. Neddylation dysfunction in Alzheimer's disease.Journal of cellular and molecular medicine · 2012
    Review
  20. Article

10 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

5 authors at 3 institutions in 3 countries.

M FurukawaLineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599-7295, USA.
Y Zhang
J McCarville
T Ohta
Y Xiong
UNC Lineberger Comprehensive Cancer CenterSegeberger Kliniken · DEUniversity of North Carolina at Chapel Hill · US

Funding

The Physiological Function and Regulation of INK4 GenesR01CA068377 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MARZLUFF, WILLIAM F. · 1995 to 2021
$6.5M
The Mammalian Cell Cycle Control and Tumor GenesisR01CA065572 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI XIONG, YUE · 1995 to 2009
$2.8M
NCI NIH HHS CA65572NCI NIH HHS CA68377NCI NIH HHS R01 CA065572NCI NIH HHS R01 CA068377
6 · The paper itself

Abstract

Members of the cullin and RING finger ROC protein families form heterodimeric complexes to constitute a potentially large number of distinct E3 ubiquitin ligases. We report here that the highly conserved C-terminal sequence in CUL1 is dually required, both for nuclear localization and for modification by NEDD8. Disruption of ROC1 binding impaired nuclear accumulation of CUL1 and decreased NEDD8 modification in vivo but had no effect on NEDD8 modification of CUL1 in vitro, suggesting that ROC1 promotes CUL1 nuclear accumulation to facilitate its NEDD8 modification. Disruption of NEDD8 binding had no effect on ROC1 binding, nor did it affect nuclear localization of CUL1, suggesting that nuclear localization and NEDD8 modification of CUL1 are two separable steps, with nuclear import preceding and required for NEDD8 modification. Disrupting NEDD8 modification diminishes the IkappaBalpha ubiquitin ligase activity of CUL1. These results identify a pathway for regulation of CUL1 activity-ROC1 and the CUL1 C-terminal sequence collaboratively mediate nuclear accumulation and NEDD8 modification, facilitating assembly of active CUL1 ubiquitin ligase. This pathway may be commonly utilized for the assembly of other cullin ligases.

Indexed as

Cullin ProteinsI-kappa B ProteinsUbiquitin-Protein Ligase ComplexesAmino Acid SequenceAnaphase-Promoting Complex-CyclosomeAnimalsBlotting, WesternCell Cycle ProteinsCell LineCell NucleusDNA-Binding ProteinsDNA, ComplementaryFluorescent Antibody Technique, IndirectHeLa CellsHumansImmunohistochemistryAnaphase-Promoting Complex-CyclosomeCell Cycle ProteinsCullin 1Cullin ProteinsDNA-Binding ProteinsDNA, ComplementaryI-kappa B ProteinsLigasesNEDD8 ProteinNEDD8 protein, humanNF-KappaB Inhibitor alphaNFKBIA protein, humanUbiquitin-Protein Ligase ComplexesUbiquitin-Protein LigasesUbiquitins

Identifiers

PMID11027288
PMCPMC86428
OpenAlexW2131250046

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.