Evidence map›Paper›PMID 11930005›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2002

Mitf and Tfe3, two members of the Mitf-Tfe family of bHLH-Zip transcription factors, have important but functionally redundant roles in osteoclast development.

Eiríkur Steingrimsson, Lino Tessarollo, Bhavani Pathak, Ling Hou, Heinz Arnheiter, Neal G Copeland, Nancy A Jenkins

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 119 papers.

0numbers the graph read from it
0cells of the map it votes in
119citing papers in PubMed
5.0field-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

119 citing papers in PubMed, 225 citations in OpenAlex.

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  10. A framework for target discovery in rare cancers.bioRxiv : the preprint server for biology · 2024
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  16. TFEB/3 Govern Repair Schwann Cell Generation and Function Following Peripheral Nerve Injury.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  17. Article
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  19. Absence of meningeal mast cells in theFrontiers in cellular neuroscience · 2024
    Article
  20. On the role of TFEC in reptilian coloration.Frontiers in cell and developmental biology · 2024
    Article

59 more citing papers are in PubMed but not listed here.

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 4 institutions in 2 countries.

Eiríkur SteingrimssonDepartment of Biochemistry and Molecular Biology, Faculty of Medicine, University of Iceland, 101 Reykjavik, Iceland. eirikurs@hi.is
Lino Tessarollo
Bhavani Pathak
Ling Hou
Heinz Arnheiter
Neal G Copeland
Nancy A Jenkins
University of Iceland · ISNational Institutes of Health · USCancer Genetics (United States) · USNational Cancer Institute · US

Funding

Transcription Regulation In Vertebrate Eye DevelopmentZIANS002790 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI ARNHEITER, HEINZ · 2009 to 2012
$3.1M
Transcription Regulation In Vertebrate Eye DevelopmentZ01NS002790 · NINDS · NEUROLOGICAL DISORDERS AND STROKE · PI ARNHEITER, HEINZ · 1990 to 2008
$2.1M
6 · The paper itself

Abstract

The Mitf-Tfe family of basic helix-loop-helix-leucine zipper (bHLH-Zip) transcription factors encodes four family members: Mitf, Tfe3, Tfeb, and Tfec. In vitro, each protein in the family can bind DNA as a homo- or heterodimer with other family members. Mutational studies in mice have shown that Mitf is essential for melanocyte and eye development, whereas Tfeb is required for placental vascularization. Here, we uncover a role for Tfe3 in osteoclast development, a role that is functionally redundant with Mitf. Although osteoclasts seem normal in Mitf or Tfe3 null mice, the combined loss of the two genes results in severe osteopetrosis. We also show that Tfec mutant mice are phenotypically normal, and that the Tfec mutation does not alter the phenotype of Mitf, Tfeb, or Tfe3 mutant mice. Surprisingly, our studies failed to identify any phenotypic overlap between the different Mitf-Tfe mutations. These results suggest that heterodimeric interactions are not essential for Mitf-Tfe function in contrast to other bHLH-Zip families like Myc/Max/Mad, where heterodimeric interactions seem to be essential.

Indexed as

AllelesAnimalsBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsCathepsin KCathepsinsDimerizationDNA-Binding ProteinsMiceMice, Inbred C57BLMicrophthalmia-Associated Transcription FactorMutationOsteoclastsOsteopetrosisTranscription FactorsBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsCathepsin KCathepsinsCTSK protein, humanCtsk protein, mouseDNA-Binding ProteinsMicrophthalmia-Associated Transcription FactorMitf protein, mouseTFE3 protein, humanTranscription Factors

Identifiers

PMID11930005
PMCPMC123673
OpenAlexW2117112828

What OpenQuestion 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 OpenQuestion graph.