Evidence map›Paper›PMID 2196440›Full record

ArticleMolecular and cellular biology1990

Enhanced translation and increased turnover of c-myc proteins occur during differentiation of murine erythroleukemia cells.

G D Spotts, S R Hann

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 1990. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

30 citing papers in PubMed, 80 citations in OpenAlex.

  1. Article
  2. IBtkα Activates the β-Catenin-Dependent Transcription ofInternational journal of molecular sciences · 2022
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  3. Altered CaCells · 2021
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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.

G D SpottsDepartment of Cell Biology, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-2175.
S R Hann
Vanderbilt University · US

Funding

MULTIDISCIPLINARY BASIC RESEARCH TRAINING IN CANCERT32CA009592 · NCI · VANDERBILT UNIVERSITY · PI Justin M Balko, Julie A Rhoades (Sterling) · 1987 to 2026
$10.4M
TWO C-MYC PROTEINS--ROLE IN CELL GROWTH &ONCOGENESISR01CA047399 · NCI · VANDERBILT UNIVERSITY · PI HANN, STEPHEN RAY · 1988 to 2005
$1.7M
ROLE OF TGF-BETA RELATED GENES IN REGULATING NORMAL EMBRYONIC DEVELOPMENTP01CA048799 · NCI · VANDERBILT UNIVERSITY · PI MOSES, HAROLD L · 1989 to 1997
–
NCI NIH HHS CA-47399NCI NIH HHS CA-48799NCI NIH HHS T32-CA-09592
6 · The paper itself

Abstract

To determine whether regulation of c-myc proteins occurs during the differentiation of murine erythroleukemia cells, we examined c-myc protein synthesis and accumulation throughout dimethyl sulfoxide (DMSO)- or hypoxanthine-induced differentiation. c-myc protein expression exhibited an overall biphasic reduction, with an initial concomitant decrease in c-myc RNA, protein synthesis, and protein accumulation early during the commitment phase. However, as the mRNA and protein levels recovered, c-myc protein synthesis levels dissociated from the levels of c-myc mRNA and protein accumulation. This dissociation appears to result from unusual translational and posttranslational regulation during differentiation. Translational enhancement was suggested by the observation that relatively high levels of c-myc proteins were synthesized from relatively moderate levels of c-myc RNA. This translational enhancement was not observed with c-myb. Under certain culture conditions, we also observed a change in the relative synthesis ratio of the two independently initiated c-myc proteins. Posttranslational regulation was evidenced by a dramatic postcommitment decrease in the accumulated c-myc protein levels despite relatively high levels of c-myc protein synthesis. This decrease corresponded with a twofold increase in the turnover of c-myc proteins. The consequence of this regulation was that the most substantial decrease in c-myc protein accumulation occurred during the postcommitment phase of differentiation. This result supports the hypothesis that the reduction in c-myc at relatively late times is most important for completion of murine erythroleukemia cell terminal differentiation.

Indexed as

Cell DifferentiationProtein BiosynthesisAnimalsBlotting, WesternCell LineDimethyl SulfoxideGene ExpressionHypoxanthineHypoxanthinesKineticsLeukemia, Erythroblastic, AcuteLeukemia, ExperimentalMiceProtein Processing, Post-TranslationalProtein-Tyrosine KinasesProto-Oncogene ProteinsDimethyl SulfoxideHypoxanthineHypoxanthinesProtein-Tyrosine KinasesProto-Oncogene ProteinsProto-Oncogene Proteins c-mycRNA, MessengerRNA, Neoplasm

Identifiers

PMID2196440
PMCPMC360906
OpenAlexW1825342026

What OpenQuestion holds

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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.