Evidence map›Paper›PMID 12215534›Full record

ArticleMolecular and cellular biology2002

Inactivation of the retinoblastoma protein family can bypass the HCF-1 defect in tsBN67 cell proliferation and cytokinesis.

Patrick T Reilly, Joanna Wysocka, Winship Herr

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

18 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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  4. The potential role of O-GlcNAc modification in cancer epigenetics.Cellular & molecular biology letters · 2014
    Review
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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

3 authors at 2 institutions in 1 country.

Patrick T ReillyCold Spring Harbor Laboratory, Cold Spring Harbor, New York 11724, USA.
Joanna Wysocka
Winship Herr
Cold Spring Harbor Laboratory · USState University of New York · US

Funding

VIRAL TRANSACTIVATIONP01CA013106 · NCI · COLD SPRING HARBOR LABORATORY · PI William Richard McCombie · 1985 to 2026
$116.8M
CELLULAR FUNCTIONS OF HCFR01GM054598 · NIGMS · COLD SPRING HARBOR LABORATORY · PI MYERS, MICHAEL P · 1996 to 2005
$1.2M
NCI NIH HHS CA13106NCI NIH HHS P01 CA013106NIGMS NIH HHS GM54598NIGMS NIH HHS R01 GM054598
6 · The paper itself

Abstract

Owing to a single missense mutation in the cell proliferation factor HCF-1, the temperature-sensitive tsBN67 hamster cell line arrests proliferation at nonpermissive temperatures, primarily in a G(0)/G(1) state, and displays temperature-sensitive cytokinesis defects. The HCF-1 mutation in tsBN67 cells also causes a temperature-sensitive dissociation of HCF-1 from chromatin prior to cell proliferation arrest, suggesting that HCF-1-chromatin association is important for mammalian-cell proliferation. Here, we report that the simian virus 40 (SV40) early region, in particular, large T antigen (Tag), and the adenovirus oncoprotein E1A can rescue the tsBN67 cell proliferation defect at nonpermissive temperatures. The SV40 early region rescues the tsBN67 cell proliferation defect without restoring the HCF-1-chromatin association, indicating that these oncoproteins bypass a requirement for HCF-1 function. The SV40 early region also rescues the tsBN67 cytokinesis defect, suggesting that the roles of HCF-1 in cell proliferation and proper cytokinesis are intimately linked. The ability of SV40 Tag and adenovirus E1A to inactivate members of the pRb protein family-pRb, p107, and p130-is important for the bypass of HCF-1 function. These results suggest that HCF-1 regulates mammalian-cell proliferation and cytokinesis, at least in part, by either directly or indirectly opposing pRb family member function.

Indexed as

Cell Cycle ProteinsDNA-Binding ProteinsAdenovirus E1A ProteinsAmino Acid MotifsAnimalsAntigens, Viral, TumorCell DivisionCell LineChromatinCricetinaeE2F Transcription FactorsHost Cell Factor C1KidneyMutation, MissenseNuclear ProteinsOncogene ProteinsAdenovirus E1A ProteinsAntigens, Viral, TumorCell Cycle ProteinsChromatinDNA-Binding ProteinsE2F Transcription FactorsHost Cell Factor C1Nuclear ProteinsOncogene ProteinsPhosphoproteinsProteinsRetinoblastoma-Like Protein p130Retinoblastoma ProteinTranscription Factors

Identifiers

PMID12215534
PMCPMC134044
OpenAlexW2153949088

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.