Differentiation of zebrafish melanophores depends on transcription factors AP2 alpha and AP2 epsilon.

A model of the gene-regulatory-network (GRN), governing growth, survival, and differentiation of melanocytes, has emerged from studies of mouse coat color mutants and melanoma cell lines. In this model, Transcription Factor Activator Protein 2 alpha (TFAP2A) contributes to melanocyte development by...

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Main Authors: Eric Van Otterloo, Wei Li, Gregory Bonde, Kristopher M Day, Mei-Yu Hsu, Robert A Cornell
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2010-09-01
Series:PLoS Genetics
Online Access:https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1001122&type=printable
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author Eric Van Otterloo
Wei Li
Gregory Bonde
Kristopher M Day
Mei-Yu Hsu
Robert A Cornell
author_facet Eric Van Otterloo
Wei Li
Gregory Bonde
Kristopher M Day
Mei-Yu Hsu
Robert A Cornell
author_sort Eric Van Otterloo
collection DOAJ
description A model of the gene-regulatory-network (GRN), governing growth, survival, and differentiation of melanocytes, has emerged from studies of mouse coat color mutants and melanoma cell lines. In this model, Transcription Factor Activator Protein 2 alpha (TFAP2A) contributes to melanocyte development by activating expression of the gene encoding the receptor tyrosine kinase Kit. Next, ligand-bound Kit stimulates a pathway activating transcription factor Microphthalmia (Mitf), which promotes differentiation and survival of melanocytes by activating expression of Tyrosinase family members, Bcl2, and other genes. The model predicts that in both Tfap2a and Kit null mutants there will be a phenotype of reduced melanocytes and that, because Tfap2a acts upstream of Kit, this phenotype will be more severe, or at least as severe as, in Tfap2a null mutants in comparison to Kit null mutants. Unexpectedly, this is not the case in zebrafish or mouse. Because many Tfap2 family members have identical DNA-binding specificity, we reasoned that another Tfap2 family member may work redundantly with Tfap2a in promoting Kit expression. We report that tfap2e is expressed in melanoblasts and melanophores in zebrafish embryos and that its orthologue, TFAP2E, is expressed in human melanocytes. We provide evidence that Tfap2e functions redundantly with Tfap2a to maintain kita expression in zebrafish embryonic melanophores. Further, we show that, in contrast to in kita mutants where embryonic melanophores appear to differentiate normally, in tfap2a/e doubly-deficient embryonic melanophores are small and under-melanized, although they retain expression of mitfa. Interestingly, forcing expression of mitfa in tfap2a/e doubly-deficient embryos partially restores melanophore differentiation. These findings reveal that Tfap2 activity, mediated redundantly by Tfap2a and Tfap2e, promotes melanophore differentiation in parallel with Mitf by an effector other than Kit. This work illustrates how analysis of single-gene mutants may fail to identify steps in a GRN that are affected by the redundant activity of related proteins.
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spelling doaj.art-8c467bde7a6d4923a6aec3322367799c2025-02-17T05:30:58ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042010-09-0169e100112210.1371/journal.pgen.1001122Differentiation of zebrafish melanophores depends on transcription factors AP2 alpha and AP2 epsilon.Eric Van OtterlooWei LiGregory BondeKristopher M DayMei-Yu HsuRobert A CornellA model of the gene-regulatory-network (GRN), governing growth, survival, and differentiation of melanocytes, has emerged from studies of mouse coat color mutants and melanoma cell lines. In this model, Transcription Factor Activator Protein 2 alpha (TFAP2A) contributes to melanocyte development by activating expression of the gene encoding the receptor tyrosine kinase Kit. Next, ligand-bound Kit stimulates a pathway activating transcription factor Microphthalmia (Mitf), which promotes differentiation and survival of melanocytes by activating expression of Tyrosinase family members, Bcl2, and other genes. The model predicts that in both Tfap2a and Kit null mutants there will be a phenotype of reduced melanocytes and that, because Tfap2a acts upstream of Kit, this phenotype will be more severe, or at least as severe as, in Tfap2a null mutants in comparison to Kit null mutants. Unexpectedly, this is not the case in zebrafish or mouse. Because many Tfap2 family members have identical DNA-binding specificity, we reasoned that another Tfap2 family member may work redundantly with Tfap2a in promoting Kit expression. We report that tfap2e is expressed in melanoblasts and melanophores in zebrafish embryos and that its orthologue, TFAP2E, is expressed in human melanocytes. We provide evidence that Tfap2e functions redundantly with Tfap2a to maintain kita expression in zebrafish embryonic melanophores. Further, we show that, in contrast to in kita mutants where embryonic melanophores appear to differentiate normally, in tfap2a/e doubly-deficient embryonic melanophores are small and under-melanized, although they retain expression of mitfa. Interestingly, forcing expression of mitfa in tfap2a/e doubly-deficient embryos partially restores melanophore differentiation. These findings reveal that Tfap2 activity, mediated redundantly by Tfap2a and Tfap2e, promotes melanophore differentiation in parallel with Mitf by an effector other than Kit. This work illustrates how analysis of single-gene mutants may fail to identify steps in a GRN that are affected by the redundant activity of related proteins.https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1001122&type=printable
spellingShingle Eric Van Otterloo
Wei Li
Gregory Bonde
Kristopher M Day
Mei-Yu Hsu
Robert A Cornell
Differentiation of zebrafish melanophores depends on transcription factors AP2 alpha and AP2 epsilon.
PLoS Genetics
title Differentiation of zebrafish melanophores depends on transcription factors AP2 alpha and AP2 epsilon.
title_full Differentiation of zebrafish melanophores depends on transcription factors AP2 alpha and AP2 epsilon.
title_fullStr Differentiation of zebrafish melanophores depends on transcription factors AP2 alpha and AP2 epsilon.
title_full_unstemmed Differentiation of zebrafish melanophores depends on transcription factors AP2 alpha and AP2 epsilon.
title_short Differentiation of zebrafish melanophores depends on transcription factors AP2 alpha and AP2 epsilon.
title_sort differentiation of zebrafish melanophores depends on transcription factors ap2 alpha and ap2 epsilon
url https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1001122&type=printable
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