Evidence map›Paper›PMID 20861300›Full record

ArticleMolecular biology of the cell2010

Paradoxical instability-activity relationship defines a novel regulatory pathway for retinoblastoma proteins.

Pankaj Acharya, Nitin Raj, Martin S Buckley, Liang Zhang, Stephanie Duperon, Geoffrey Williams, R William Henry, David N Arnosti

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.6field-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

13 citing papers in PubMed, 19 citations in OpenAlex.

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  3. Selective repression of the Drosophila cyclin B promoter by retinoblastoma and E2F proteins.Biochimica et biophysica acta. Gene regulatory mechanisms · 2020
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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

8 authors at 3 institutions in 2 countries.

Pankaj AcharyaDepartment of Microbiology and Molecular Genetics, Program in Genetics, Michigan State University, East Lansing, MI 48824-1319, USA.
Nitin Raj
Martin S Buckley
Liang Zhang
Stephanie Duperon
Geoffrey Williams
R William Henry
David N Arnosti
Michigan State University · USBrown University · USLaboratory of Molecular Genetics · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The retinoblastoma (RB) transcriptional corepressor and related family of pocket proteins play central roles in cell cycle control and development, and the regulatory networks governed by these factors are frequently inactivated during tumorigenesis. During normal growth, these proteins are subject to tight control through at least two mechanisms. First, during cell cycle progression, repressor potential is down-regulated by Cdk-dependent phosphorylation, resulting in repressor dissociation from E2F family transcription factors. Second, RB proteins are subject to proteasome-mediated destruction during development. To better understand the mechanism for RB family protein instability, we characterized Rbf1 turnover in Drosophila and the protein motifs required for its destabilization. We show that specific point mutations in a conserved C-terminal instability element strongly stabilize Rbf1, but strikingly, these mutations also cripple repression activity. Rbf1 is destabilized specifically in actively proliferating tissues of the larva, indicating that controlled degradation of Rbf1 is linked to developmental signals. The positive linkage between Rbf1 activity and its destruction indicates that repressor function is governed in a manner similar to that described by the degron theory of transcriptional activation. Analogous mutations in the mammalian RB family member p107 similarly induce abnormal accumulation, indicating substantial conservation of this regulatory pathway.

Indexed as

Signal TransductionAmino Acid SequenceAnimalsAnimals, Genetically ModifiedBlotting, WesternCell LineCysteine Proteinase InhibitorsDrosophila melanogasterDrosophila ProteinsE2F Transcription FactorsEyeFemaleLarvaLeupeptinsMaleMolecular Sequence Databenzyloxycarbonylleucyl-leucyl-leucine aldehydeCysteine Proteinase InhibitorsDrosophila ProteinsE2F Transcription FactorsLeupeptinsRbf protein, DrosophilaRetinoblastoma-Like Protein p107Retinoblastoma ProteinTranscription Factors

Identifiers

PMID20861300
PMCPMC2982090
OpenAlexW2101033848

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.