Evidence map›Paper›PMID 12446761›Full record

ArticleMolecular and cellular biology2002

Multiple developmental defects derived from impaired recruitment of ASC-2 to nuclear receptors in mice: implication for posterior lenticonus with cataract.

Seung-Whan Kim, Cheolho Cheong, Young-Chang Sohn, Young-Hwa Goo, Wan Je Oh, Jung Hwan Park, So Young Joe, Hyen-Sam Kang, Duk-Kyung Kim, Changwon Kee and 2 more

Abstract read
In one paragraph

Article in Molecular and cellular biology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

17 citing papers in PubMed, 29 citations in OpenAlex.

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  9. Roles of histone H3-lysine 4 methyltransferase complexes in NR-mediated gene transcription.Progress in molecular biology and translational science · 2009
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  13. Coactivator as a target gene specificity determinant for histone H3 lysine 4 methyltransferases.Proceedings of the National Academy of Sciences of the United States of America · 2006
    Article
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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

12 authors at 4 institutions in 3 countries.

Seung-Whan KimDepartment of Life Science, Pohang University of Science and Technology, Pohang 790-784, Korea.
Cheolho Cheong
Young-Chang Sohn
Young-Hwa Goo
Wan Je Oh
Jung Hwan Park
So Young Joe
Hyen-Sam Kang
Duk-Kyung Kim
Changwon Kee
Jae Woon Lee
Han-Woong Lee
Samsung (United States) · USPohang University of Science and Technology · KRSeoul National University · KRSamsung Medical Center · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ASC-2, a recently isolated transcriptional coactivator molecule, stimulates transactivation by multiple transcription factors, including nuclear receptors. We generated a potent dominant negative fragment of ASC-2, encompassing the N-terminal LXXLL motif that binds a broad range of nuclear receptors. This fragment, termed DN1, specifically inhibited endogenous ASC-2 from binding these receptors in vivo, whereas DN1/m, in which the LXXLL motif was mutated to LXXAA to abolish the receptor interactions, was inert. Interestingly, DN1 transgenic mice but not DN1/m transgenic mice exhibited severe microphthalmia and posterior lenticonus with cataract as well as a variety of pathophysiological phenotypes in many other organs. Our results provide a novel insight into the molecular and histopathological mechanism of posterior lenticonus with cataract and attest to the importance of ASC-2 as a pivotal transcriptional coactivator of nuclear receptors in vivo.

Indexed as

Congenital AbnormalitiesIntracellular Signaling Peptides and ProteinsAmino Acid MotifsAnimalsCells, CulturedDisease Models, AnimalEmbryo, MammalianEyeFemaleFibroblastsGenes, LethalGenes, ReporterHumansLens DiseasesMiceMice, TransgenicIntracellular Signaling Peptides and ProteinsNCOA6 protein, humanNcoa6 protein, mouseNuclear Receptor CoactivatorsPeptide FragmentsReceptors, Cytoplasmic and NuclearReceptors, Retinoic AcidTranscription Factors

Identifiers

PMID12446761
PMCPMC139866
OpenAlexW2126495126

What Socratic 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 Socratic graph.