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The Eyes Absent proteins in development and in developmental disorders

The Eyes Absent (EYA) transactivator-phosphatase proteins are important contributors to cell-fate determination processes and to the development of multiple organs. The transcriptional regulatory activity as well as the protein tyrosine phosphatase activities of the EYA proteins can independently co...

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Autores principales: Soni, Upendra Kumar, Roychoudhury, Kaushik, Hegde, Rashmi S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8286820/
https://www.ncbi.nlm.nih.gov/pubmed/34196366
http://dx.doi.org/10.1042/BST20201302
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author Soni, Upendra Kumar
Roychoudhury, Kaushik
Hegde, Rashmi S.
author_facet Soni, Upendra Kumar
Roychoudhury, Kaushik
Hegde, Rashmi S.
author_sort Soni, Upendra Kumar
collection PubMed
description The Eyes Absent (EYA) transactivator-phosphatase proteins are important contributors to cell-fate determination processes and to the development of multiple organs. The transcriptional regulatory activity as well as the protein tyrosine phosphatase activities of the EYA proteins can independently contribute to proliferation, differentiation, morphogenesis and tissue homeostasis in different contexts. Aberrant EYA levels or activity are associated with numerous syndromic and non-syndromic developmental disorders, as well as cancers. Commensurate with the multiplicity of biochemical activities carried out by the EYA proteins, they impact upon a range of cellular signaling pathways. Here, we provide a broad overview of the roles played by EYA proteins in development, and highlight the molecular signaling pathways known to be linked with EYA-associated organ development and developmental disorders.
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spelling pubmed-82868202021-08-02 The Eyes Absent proteins in development and in developmental disorders Soni, Upendra Kumar Roychoudhury, Kaushik Hegde, Rashmi S. Biochem Soc Trans Review Articles The Eyes Absent (EYA) transactivator-phosphatase proteins are important contributors to cell-fate determination processes and to the development of multiple organs. The transcriptional regulatory activity as well as the protein tyrosine phosphatase activities of the EYA proteins can independently contribute to proliferation, differentiation, morphogenesis and tissue homeostasis in different contexts. Aberrant EYA levels or activity are associated with numerous syndromic and non-syndromic developmental disorders, as well as cancers. Commensurate with the multiplicity of biochemical activities carried out by the EYA proteins, they impact upon a range of cellular signaling pathways. Here, we provide a broad overview of the roles played by EYA proteins in development, and highlight the molecular signaling pathways known to be linked with EYA-associated organ development and developmental disorders. Portland Press Ltd. 2021-06-30 2021-07-01 /pmc/articles/PMC8286820/ /pubmed/34196366 http://dx.doi.org/10.1042/BST20201302 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Review Articles
Soni, Upendra Kumar
Roychoudhury, Kaushik
Hegde, Rashmi S.
The Eyes Absent proteins in development and in developmental disorders
title The Eyes Absent proteins in development and in developmental disorders
title_full The Eyes Absent proteins in development and in developmental disorders
title_fullStr The Eyes Absent proteins in development and in developmental disorders
title_full_unstemmed The Eyes Absent proteins in development and in developmental disorders
title_short The Eyes Absent proteins in development and in developmental disorders
title_sort eyes absent proteins in development and in developmental disorders
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8286820/
https://www.ncbi.nlm.nih.gov/pubmed/34196366
http://dx.doi.org/10.1042/BST20201302
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