Evidence map›Paper›PMID 18070929›Full record

ArticleMolecular and cellular biology2008

A non-tumor suppressor role for basal p19ARF in maintaining nucleolar structure and function.

Anthony J Apicelli, Leonard B Maggi, Angela C Hirbe, Alexander P Miceli, Mary E Olanich, Crystal L Schulte-Winkeler, Anthony J Saporita, Michael Kuchenreuther, José Sanchez, Katherine Weilbaecher and 1 more

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

28 citing papers in PubMed, 41 citations in OpenAlex.

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  15. Insights into the regulation of neuronal viability by nucleophosmin/B23.Experimental biology and medicine (Maywood, N.J.) · 2015
    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

11 authors at 3 institutions in 2 countries.

Anthony J ApicelliDepartment of Internal Medicine, Division of Molecular Oncology, Washington University School of Medicine, Campus Box 8069, 660 S. Euclid Avenue, St. Louis, MO 63110, USA. jweber@im.wustl.edu
Leonard B Maggi
Angela C Hirbe
Alexander P Miceli
Mary E Olanich
Crystal L Schulte-Winkeler
Anthony J Saporita
Michael Kuchenreuther
José Sanchez
Katherine Weilbaecher
Jason D Weber
Molecular Oncology (United States) · USInstitute of Cell Biology and Neurobiology · ITWashington University in St. Louis · US

Funding

Characterization of p53-independent ARF pathwayR01GM066032 · NIGMS · WASHINGTON UNIVERSITY · PI WEBER, JASON · 2003 to 2007
$1.3M
NIGMS NIH HHS GM066032NIGMS NIH HHS R01 GM066032
6 · The paper itself

Abstract

The nucleolus is the center of ribosome synthesis, with the nucleophosmin (NPM) and p19(ARF) proteins antagonizing one another to either promote or inhibit growth. However, basal NPM and ARF proteins form nucleolar complexes whose functions remain unknown. Nucleoli from Arf(-/)(-) cells displayed increased nucleolar area, suggesting that basal ARF might regulate key nucleolar functions. Concordantly, ribosome biogenesis and protein synthesis were dramatically elevated in the absence of Arf, causing these cells to exhibit tremendous gains in protein amounts and increases in cell volume. The transcription of ribosomal DNA (rDNA), the processing of nascent rRNA molecules, and the nuclear export of ribosomes were all increased in the absence of ARF. Similar results were obtained using targeted lentiviral RNA interference of ARF in wild-type MEFs. Postmitotic osteoclasts from Arf-null mice exhibited hyperactivity in vitro and in vivo, demonstrating a physiological function for basal ARF. Moreover, the knockdown of NPM blocked the increases in Arf(-/-) ribosome output and osteoclast activity, demonstrating that these gains require NPM. Thus, basal ARF proteins act as a monitor of steady-state ribosome biogenesis and growth independent of their ability to prevent unwarranted hyperproliferation.

Indexed as

AnimalsCell NucleolusCyclin-Dependent Kinase Inhibitor p16DNA, RibosomalMiceNuclear ProteinsNucleophosminProtein BiosynthesisRibosomesRNA, RibosomalTranscription, GeneticTumor Suppressor ProteinsCdkn2a protein, mouseCyclin-Dependent Kinase Inhibitor p16DNA, RibosomalNuclear ProteinsNucleophosminRNA, RibosomalTumor Suppressor Proteins

Identifiers

PMID18070929
PMCPMC2223401
OpenAlexW2022590421

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.