Evidence map›Paper›PMID 8927054›Full record

ArticleMolecular and cellular biology1996

Two new members of the murine Sim gene family are transcriptional repressors and show different expression patterns during mouse embryogenesis.

M Ema, M Morita, S Ikawa, M Tanaka, Y Matsuda, O Gotoh, Y Saijoh, H Fujii, H Hamada, Y Kikuchi and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

46 citing papers in PubMed, 160 citations in OpenAlex.

  1. Aryl hydrocarbon receptor nuclear translocator 2: a forgotten per-ARNT-Sim transcription factor.Toxicological sciences : an official journal of the Society of Toxicology · 2026
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  17. bHLH-PAS proteins in cancer.Nature reviews. Cancer · 2013
    Review
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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

11 authors at 3 institutions in 1 country.

M EmaDepartment of Chemistry, Graduate School of Science, Tohoku University, Sendai, Japan.
M Morita
S Ikawa
M Tanaka
Y Matsuda
O Gotoh
Y Saijoh
H Fujii
H Hamada
Y Kikuchi
Y Fujii-Kuriyama
Tohoku University · JPTokyo Metropolitan Institute of Medical Science · JPSaitama Cancer Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

From a cDNA library of mouse skeletal muscle, we have isolated mouse Sim1 (mSim1) cDNA encoding a polypeptide of 765 amino acids with striking amino acid identify in basic helix-loop-helix (89% identify) and PAS (89 % identify) domains to previously identified mSim2, although the carboxy-terminal third of the molecule did not show any similarity to mSim2 or Drosophila Sim (dSim). Yeast two-hybrid analysis and coimmunoprecipitation experiments demonstrated that both of the mSim gene products interacted with Arnt even more efficiently than AhR, a natural partner of Arnt, suggesting a functional cooperativity with Arnt. In sharp contrast with dSim having transcriptional-enhancing activity in the carboxy-terminal region, the two mSims possessed a repressive activity toward Arnt in the heterodimer complex. This is the first example of bHLH-PAS proteins with transrepressor activity, although some genetic data suggest that dSim plays a repressive role in gene expression (Z. Chang, D. Price, S. Bockheim, M. J. Boedigheimer, R. Smith, and A. Laughon, Dev. Biol. 160:315-322, 1993; D. M. Mellerick and M. Nirenberg, Dev. Biol. 171:306-316, 1995). Whole-mount in situ hybridization showed restricted and characteristic expression patterns of the two mSim mRNAs in various tissues and organs during embryogenesis, such as those for the somite, the nephrogenic cord, and the mesencephalon (for mSim1) and those for the diencephalon, branchial arches, and limbs (for mSim2). From sequence similarity and chromosomal localization, it is concluded that mSim2 is an ortholog of hSim2, which is proposed to be a candidate gene responsible for Down's syndrome. The sites of mSim2 expression showed an overlap with the affected regions of the syndrome, further strengthening involvement of mSim2 in Down's syndrome.

Indexed as

Chromosome MappingGene Expression Regulation, DevelopmentalMultigene FamilyAmino Acid SequenceAnimalsBasic Helix-Loop-Helix ProteinsBrainCell LineCloning, MolecularCOS CellsDNA-Binding ProteinsDrosophilaDrosophila ProteinsEmbryonic and Fetal DevelopmentGene LibraryHelix-Loop-Helix MotifsBasic Helix-Loop-Helix ProteinsDNA-Binding ProteinsDrosophila ProteinsNuclear ProteinsRecombinant Fusion ProteinsRecombinant ProteinsRepressor ProteinsRNA ProbesSIM1 protein, humanSim1 protein, mousesim protein, Drosophila

Identifiers

PMID8927054
PMCPMC231588
OpenAlexW2159527243

What OpenQuestion holds

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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.