Evidence map›Paper›PMID 28249010›Full record

ArticlePLoS genetics2017

TFAP2 paralogs regulate melanocyte differentiation in parallel with MITF.

Hannah E Seberg, Eric Van Otterloo, Stacie K Loftus, Huan Liu, Greg Bonde, Ramakrishna Sompallae, Derek E Gildea, Juan F Santana, J Robert Manak, William J Pavan and 2 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

57 citing papers in PubMed, 100 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Mgat4b-mediated selectiveProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  9. Article
  10. Article
  11. From neural crest migration to the onset of gangliogenesis.Current topics in developmental biology · 2025
    Review
  12. Review
  13. Article
  14. Microneedles: A novel clinical technology for evaluating skin characteristics.Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI) · 2024
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 1 country.

Hannah E SebergInterdisciplinary Graduate Program in Genetics, University of Iowa, Iowa City, Iowa, United States of America.ORCID 0000-0003-3846-6132
Eric Van OtterlooSDM-Craniofacial Biology, University of Colorado - Anschutz Medical Campus, Aurora, Colorado, United States of America.ORCID 0000-0001-5958-5742
Stacie K LoftusGenetic Disease Research Branch, National Human Genome Research Institute, NIH, Bethesda, Maryland, United States of America.
Huan LiuDepartment of Anatomy and Cell Biology, University of Iowa, Iowa City, Iowa, United States of America.
Greg BondeDepartment of Anatomy and Cell Biology, University of Iowa, Iowa City, Iowa, United States of America.ORCID 0000-0002-9808-5430
Ramakrishna SompallaeBioinformatics Division, Iowa Institute of Human Genetics, University of Iowa, Iowa City, Iowa, United States of America.
Derek E GildeaBioinformatics and Scientific Programming Core, Computational and Statistical Genomics Branch, National Human Genome Research Institute, NIH, Bethesda, Maryland, United States of America.
Juan F SantanaDepartment of Biology, University of Iowa, Iowa City, Iowa, United States of America.
J Robert ManakInterdisciplinary Graduate Program in Genetics, University of Iowa, Iowa City, Iowa, United States of America.
William J PavanGenetic Disease Research Branch, National Human Genome Research Institute, NIH, Bethesda, Maryland, United States of America.
Trevor WilliamsSDM-Craniofacial Biology, University of Colorado - Anschutz Medical Campus, Aurora, Colorado, United States of America.
Robert A CornellInterdisciplinary Graduate Program in Genetics, University of Iowa, Iowa City, Iowa, United States of America.
University of Iowa · USNational Human Genome Research Institute · USUniversity of Colorado Anschutz Medical Campus · US

Funding

Viral VectorP30CA086862 · NCI · UNIVERSITY OF IOWA · PI Douglas Robert Spitz · 2000 to 2026
$70.0M
Function genomic analysis of neural crest developmentZIAHG000136 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI PAVAN, WILLIAM J · 2009 to 2023
$13.6M
THE ROLE OF AP-2 IN CRANIOFACIAL DEVELOPMENTR01DE012728 · NIDCR · YALE UNIVERSITY · PI WILLIAMS, TREVOR J · 1998 to 2013
$5.5M
PREDOCTORAL TRAINING PROGRAM IN GENETICST32GM008629 · NIGMS · UNIVERSITY OF IOWA · PI EBERL, DANIEL F · 1997 to 2021
$4.1M
Regulation of the Melanocyte Lineage by the AP2 Transcription Factor FamilyR01AR062547 · NIAMS · UNIVERSITY OF WASHINGTON · PI CORNELL, ROBERT AARON · 2013 to 2022
$3.8M
Deciphering the role of mediator of ErbB2 driven cell motility (Memo1) in regulatF32DE023709 · NIDCR · UNIVERSITY OF COLORADO DENVER · PI VAN OTTERLOO, ERIC · 2014 to 2016
$174k
NIAMS NIH HHS R01 AR062547NIDCR NIH HHS F32 DE023709NIDCR NIH HHS R01 DE012728NIGMS NIH HHS T32 GM008629
6 · The paper itself

Abstract

Mutations in the gene encoding transcription factor TFAP2A result in pigmentation anomalies in model organisms and premature hair graying in humans. However, the pleiotropic functions of TFAP2A and its redundantly-acting paralogs have made the precise contribution of TFAP2-type activity to melanocyte differentiation unclear. Defining this contribution may help to explain why TFAP2A expression is reduced in advanced-stage melanoma compared to benign nevi. To identify genes with TFAP2A-dependent expression in melanocytes, we profile zebrafish tissue and mouse melanocytes deficient in Tfap2a, and find that expression of a small subset of genes underlying pigmentation phenotypes is TFAP2A-dependent, including Dct, Mc1r, Mlph, and Pmel. We then conduct TFAP2A ChIP-seq in mouse and human melanocytes and find that a much larger subset of pigmentation genes is associated with active regulatory elements bound by TFAP2A. These elements are also frequently bound by MITF, which is considered the "master regulator" of melanocyte development. For example, the promoter of TRPM1 is bound by both TFAP2A and MITF, and we show that the activity of a minimal TRPM1 promoter is lost upon deletion of the TFAP2A binding sites. However, the expression of Trpm1 is not TFAP2A-dependent, implying that additional TFAP2 paralogs function redundantly to drive melanocyte differentiation, which is consistent with previous results from zebrafish. Paralogs Tfap2a and Tfap2b are both expressed in mouse melanocytes, and we show that mouse embryos with Wnt1-Cre-mediated deletion of Tfap2a and Tfap2b in the neural crest almost completely lack melanocytes but retain neural crest-derived sensory ganglia. These results suggest that TFAP2 paralogs, like MITF, are also necessary for induction of the melanocyte lineage. Finally, we observe a genetic interaction between tfap2a and mitfa in zebrafish, but find that artificially elevating expression of tfap2a does not increase levels of melanin in mitfa hypomorphic or loss-of-function mutants. Collectively, these results show that TFAP2 paralogs, operating alongside lineage-specific transcription factors such as MITF, directly regulate effectors of terminal differentiation in melanocytes. In addition, they suggest that TFAP2A activity, like MITF activity, has the potential to modulate the phenotype of melanoma cells.

Indexed as

AnimalsBase SequenceBinding SitesCell DifferentiationCell LineCell Line, TumorCells, CulturedEmbryo, MammalianEmbryo, NonmammalianGene Expression ProfilingGene Expression Regulation, DevelopmentalHumansMelanocytesMice, KnockoutMicrophthalmia-Associated Transcription FactorMicroscopy, ConfocalMicrophthalmia-Associated Transcription FactorTranscription Factor AP-2Zebrafish Proteins

Identifiers

PMID28249010
PMCPMC5352137
OpenAlexW2592875818

What OpenQuestion holds

Textmetadata
LicenceCC0
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.