Evidence map›Paper›PMID 1360287›Full record

ArticleGene expression1992

The role of the promoter in the expression of the PCNA gene.

R H Charollais, H Alder, A Ferber, J Koniecki, C Sell, R Baserga

Abstract read
In one paragraph

Article in Gene expression, 1992. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 53% 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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. Article
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

6 authors at 1 institution in 1 country.

R H CharollaisJefferson Cancer Institute, Thomas Jefferson University, Philadelphia, Pennsylvania 19107-5541.
H Alder
A Ferber
J Koniecki
C Sell
R Baserga
Thomas Jefferson University · US

Funding

BIOLOGY OF THE P53 PROTEINR01GM033694 · NIGMS · THOMAS JEFFERSON UNIVERSITY · PI BASERGA, RENATO LUIGI · 1985 to 1999
–
THE BIOLOGY OF CELL CYCLE MUTANTSR01GM042383 · NIGMS · THOMAS JEFFERSON UNIVERSITY · PI BASERGA, RENATO LUIGI · 1989 to 1991
–
NIGMS NIH HHS GM-33694NIGMS NIH HHS GM-42383
6 · The paper itself

Abstract

G1-specific temperature-sensitive (ts) mutants of the cell cycle arrest in G1 after serum stimulation at the restrictive temperature. Under these conditions, the RNA levels of late growth-regulated genes (such as DNA polymerase alpha, PCNA, thymidine kinase, and core histones) are markedly decreased or even undetectable, while early growth-regulated genes (for instance, c-myc) are normally expressed, and certain promoters are actually super-induced. We have used the human PCNA gene transfected into TK-ts13 cells (a G1-specific ts mutant) to investigate whether the inhibition of gene expression caused by this type of growth inhibition occurs at a transcriptional or post-transcriptional level. Constructs were made in which the 5' and 3' flanking sequences of the human PCNA gene were replaced by the corresponding elements of the SV40 T antigen coding gene. Using these constructs and data from run-on assays and RT-PCR, we conclude that the failure of expression of the PCNA gene in G1-arrested TK-ts13 cells occurs at the transcriptional level.

Indexed as

Promoter Regions, GeneticTranscription, GeneticAnimalsCell CycleCell LineCricetinaeDNA-Directed DNA PolymeraseDNA Polymerase IIIFibroblastsGene ExpressionGenes, SyntheticHumansMesocricetusNuclear ProteinsProliferating Cell Nuclear AntigenRecombinant Fusion ProteinsDNA-Directed DNA PolymeraseDNA Polymerase IIINuclear ProteinsProliferating Cell Nuclear AntigenRecombinant Fusion Proteins

Identifiers

PMID1360287
PMCPMC6057379
OpenAlexW2415379711

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.