Evidence map›Paper›PMID 16449662›Full record

ArticleMolecular and cellular biology2006

An E2F binding-deficient Rb1 protein partially rescues developmental defects associated with Rb1 nullizygosity.

Huifang Sun, Yanjie Chang, Brett Schweers, Michael A Dyer, Xiaojing Zhang, Simon W Hayward, David W Goodrich

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

21 citing papers in PubMed, 37 citations in OpenAlex.

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  15. E2f binding-deficient Rb1 protein suppresses prostate tumor progression in vivo.Proceedings of the National Academy of Sciences of the United States of America · 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

7 authors at 3 institutions in 1 country.

Huifang SunDepartment of Pharmacology & Therapeutics, Roswell Park Cancer Institute, Elm & Carlton Streets, Buffalo, NY 14263, USA.
Yanjie Chang
Brett Schweers
Michael A Dyer
Xiaojing Zhang
Simon W Hayward
David W Goodrich
Roswell Park Comprehensive Cancer Center · USSt. Jude Children's Research Hospital · USVanderbilt University Medical Center · US

Funding

Proliferation Control in the Retina: The Rb FamilyR01EY014867 · NEI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI DYER, MICHAEL A · 2003 to 2012
$4.5M
Requirements for Normal Rb Function In VivoR01CA070292 · NCI · UNIVERSITY OF TEXAS MD ANDERSON CAN CTR · PI GOODRICH, DAVID W. · 1996 to 2010
$2.9M
Hormonal Carcinogenesis in Rb-knockout Mouse ProstateU01CA096403 · NCI · VANDERBILT UNIVERSITY · PI HAYWARD, SIMON W. · 2001 to 2005
$1.6M
NCI NIH HHS CA70292NCI NIH HHS CA96403NCI NIH HHS R01 CA070292NCI NIH HHS U01 CA096403NEI NIH HHS EY014867NEI NIH HHS R01 EY014867
6 · The paper itself

Abstract

Rb1 is essential for normal embryonic development, as null mice die in midgestation with widespread unscheduled cell proliferation. Rb1 protein (pRb) mediates cell cycle control by binding E2F transcription factors and repressing expression from E2F-dependent promoters. An increasing amount of evidence suggests that pRb loss also compromises cellular differentiation. Since differentiation is often dependent on cell cycle exit, it is currently unclear whether the effects of pRb on differentiation are an indirect consequence of pRb/E2F-mediated cell cycle control or whether they reflect direct cell-type-specific pRb functions. We have mutated Rb1 in the mouse to express a protein (R654W) specifically deficient in binding E2F1, E2F2, and E2F3. R654W mutant embryos exhibit cell cycle defects the same as those of Rb1 null embryos, reinforcing the importance of the interactions of pRb with E2F1, E2F2, and E2F3 for cell cycle control. However, R654W embryos survive at least 2 days longer than Rb1 null embryos, and increased life span is associated with improved erythrocyte and fetal liver macrophage differentiation. In contrast, R654W pRb does not rescue differentiation defects associated with pRb-deficient retinae. These data indicate that Rb1 makes important cell-type-specific contributions to cellular differentiation that are genetically separable from its general ability to stably bind E2F1, E2F2, and E2F3 and regulate the cell cycle.

Indexed as

AllelesAmino Acid SubstitutionAnimalsBase SequenceCell CycleCongenital AbnormalitiesDNAE2F Transcription FactorsFemaleFetal DevelopmentHomozygoteMaleMiceMice, KnockoutMice, Mutant StrainsMutagenesis, Site-DirectedDNAE2F Transcription FactorsRecombinant ProteinsRetinoblastoma Protein

Identifiers

PMID16449662
PMCPMC1367194
OpenAlexW2141712789

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.