Evidence map›Paper›PMID 11314044›Full record

ArticleOncogene2001

Phosphorylation of serines 15 and 37 is necessary for efficient accumulation of p53 following irradiation with UV.

L J Bean, G R Stark

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Oncogene, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

27 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
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  4. Ubiquitin proteasomal pathway mediated degradation of p53 in melanoma.Archives of biochemistry and biophysics · 2011
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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

2 authors at 1 institution in 1 country.

L J BeanDepartment of Molecular Biology, Lerner Research Institute, The Cleveland Clinic Foundation, 9500 Euclid Avenue, Cleveland, Ohio, OH 44195, USA.
G R Stark
Cleveland Clinic · US

Funding

TRAINING IN GENETICST32GM008613 · NIGMS · CASE WESTERN RESERVE UNIVERSITY · PI SALZ, HELEN KAREN · 1996 to 2010
$3.1M
P53 MODIFICATION AND NOVEL BIOLOGICAL FUNCTIONSR01GM049345 · NIGMS · CLEVELAND CLINIC LERNER COL/MED-CWRU · PI STARK, GEORGE ROBERT · 1993 to 2006
$2.5M
NIGMS NIH HHS 5-T32-GM08613NIGMS NIH HHS GM49345
6 · The paper itself

Abstract

Changes in the phosphorylation state of p53 are important in increasing its half-life and potency as a transcription factor. To investigate their roles, serine residues 15 and 37 were mutated to alanines and the mutated proteins were expressed stably at low basal levels in Li-Fraumeni-derived p53-null human fibroblasts. The accumulation of p53 after DNA damage was analysed quantitatively in multiple clones. Mutation of serine 15, serine 37 or both impaired the accumulation of the protein after exposing the cells to ultraviolet radiation (50-100% increase for the mutant proteins, 500% increase for wild-type p53) but not after treatment with adriamycin. The diminished accumulation of mutant p53 protein is due to a reduction of basal HDM association. Analysis of p53-dependent transcription revealed that phosphorylation of serine 15 is required to maintain basal levels of p21 mRNA. These results provide new evidence for an important function of serine 37 phosphorylation, clearly distinguish the pathways of p53 activation in response to ultraviolet radiation or DNA damage inflicted by adriamycin, and reveal that serine 15 is crucial to support the p53-mediated basal expression of p21.

Indexed as

Nuclear ProteinsAntineoplastic AgentsBlotting, NorthernCell LineCyclin-Dependent Kinase Inhibitor p21CyclinsDNADNA PrimersDoxorubicinFibroblastsGADD45 ProteinsGenetic VectorsHumansIntracellular Signaling Peptides and ProteinsMutationPhosphorylationAntineoplastic AgentsCDKN1A protein, humanCyclin-Dependent Kinase Inhibitor p21CyclinsDNADNA PrimersDoxorubicinGADD45 ProteinsIntracellular Signaling Peptides and ProteinsMDM2 protein, humanNuclear ProteinsProteinsProto-Oncogene ProteinsProto-Oncogene Proteins c-mdm2SerineTumor Suppressor Protein p53

Identifiers

PMID11314044
OpenAlexW2316337840

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.