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The AP-2 family of transcription factors

The AP-2 family of transcription factors consists of five different proteins in humans and mice: AP-2α, AP-2β, AP-2γ, AP-2δ and AP-2ε. Frogs and fish have known orthologs of some but not all of these proteins, and homologs of the family are also found in protochordates, insects and nematodes. The pr...

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Detalles Bibliográficos
Autores principales: Eckert, Dawid, Buhl, Sandra, Weber, Susanne, Jäger, Richard, Schorle, Hubert
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1414101/
https://www.ncbi.nlm.nih.gov/pubmed/16420676
http://dx.doi.org/10.1186/gb-2005-6-13-246
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author Eckert, Dawid
Buhl, Sandra
Weber, Susanne
Jäger, Richard
Schorle, Hubert
author_facet Eckert, Dawid
Buhl, Sandra
Weber, Susanne
Jäger, Richard
Schorle, Hubert
author_sort Eckert, Dawid
collection PubMed
description The AP-2 family of transcription factors consists of five different proteins in humans and mice: AP-2α, AP-2β, AP-2γ, AP-2δ and AP-2ε. Frogs and fish have known orthologs of some but not all of these proteins, and homologs of the family are also found in protochordates, insects and nematodes. The proteins have a characteristic helix-span-helix motif at the carboxyl terminus, which, together with a central basic region, mediates dimerization and DNA binding. The amino terminus contains the transactivation domain. AP-2 proteins are first expressed in primitive ectoderm of invertebrates and vertebrates; in vertebrates, they are also expressed in the emerging neural-crest cells, and AP-2α(-/- )animals have impairments in neural-crest-derived facial structures. AP-2β is indispensable for kidney development and AP-2γ is necessary for the formation of trophectoderm cells shortly after implantation; AP-2α and AP-2γ levels are elevated in human mammary carcinoma and seminoma. The general functions of the family appear to be the cell-type-specific stimulation of proliferation and the suppression of terminal differentiation during embryonic development.
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spelling pubmed-14141012006-03-28 The AP-2 family of transcription factors Eckert, Dawid Buhl, Sandra Weber, Susanne Jäger, Richard Schorle, Hubert Genome Biol Protein Family Review The AP-2 family of transcription factors consists of five different proteins in humans and mice: AP-2α, AP-2β, AP-2γ, AP-2δ and AP-2ε. Frogs and fish have known orthologs of some but not all of these proteins, and homologs of the family are also found in protochordates, insects and nematodes. The proteins have a characteristic helix-span-helix motif at the carboxyl terminus, which, together with a central basic region, mediates dimerization and DNA binding. The amino terminus contains the transactivation domain. AP-2 proteins are first expressed in primitive ectoderm of invertebrates and vertebrates; in vertebrates, they are also expressed in the emerging neural-crest cells, and AP-2α(-/- )animals have impairments in neural-crest-derived facial structures. AP-2β is indispensable for kidney development and AP-2γ is necessary for the formation of trophectoderm cells shortly after implantation; AP-2α and AP-2γ levels are elevated in human mammary carcinoma and seminoma. The general functions of the family appear to be the cell-type-specific stimulation of proliferation and the suppression of terminal differentiation during embryonic development. BioMed Central 2005 2005-12-28 /pmc/articles/PMC1414101/ /pubmed/16420676 http://dx.doi.org/10.1186/gb-2005-6-13-246 Text en Copyright © 2005 BioMed Central Ltd
spellingShingle Protein Family Review
Eckert, Dawid
Buhl, Sandra
Weber, Susanne
Jäger, Richard
Schorle, Hubert
The AP-2 family of transcription factors
title The AP-2 family of transcription factors
title_full The AP-2 family of transcription factors
title_fullStr The AP-2 family of transcription factors
title_full_unstemmed The AP-2 family of transcription factors
title_short The AP-2 family of transcription factors
title_sort ap-2 family of transcription factors
topic Protein Family Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1414101/
https://www.ncbi.nlm.nih.gov/pubmed/16420676
http://dx.doi.org/10.1186/gb-2005-6-13-246
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