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HERCing: Structural and Functional Relevance of the Large HERC Ubiquitin Ligases
Homologous to the E6AP carboxyl terminus (HECT) and regulator of chromosome condensation 1 (RCC1)-like domain-containing proteins (HERCs) belong to the superfamily of ubiquitin ligases. HERC proteins are divided into two subfamilies, Large and Small HERCs. Despite their similarities in terms of both...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6692442/ https://www.ncbi.nlm.nih.gov/pubmed/31447701 http://dx.doi.org/10.3389/fphys.2019.01014 |
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author | García-Cano, Jesús Martinez-Martinez, Arturo Sala-Gaston, Joan Pedrazza, Leonardo Rosa, Jose Luis |
author_facet | García-Cano, Jesús Martinez-Martinez, Arturo Sala-Gaston, Joan Pedrazza, Leonardo Rosa, Jose Luis |
author_sort | García-Cano, Jesús |
collection | PubMed |
description | Homologous to the E6AP carboxyl terminus (HECT) and regulator of chromosome condensation 1 (RCC1)-like domain-containing proteins (HERCs) belong to the superfamily of ubiquitin ligases. HERC proteins are divided into two subfamilies, Large and Small HERCs. Despite their similarities in terms of both structure and domains, these subfamilies are evolutionarily very distant and result from a convergence phenomenon rather than from a common origin. Large HERC genes, HERC1 and HERC2, are present in most metazoan taxa. They encode very large proteins (approximately 5,000 amino acid residues in a single polypeptide chain) that contain more than one RCC1-like domain as a structural characteristic. Accumulating evidences show that these unusually large proteins play key roles in a wide range of cellular functions which include neurodevelopment, DNA damage repair, and cell proliferation. To better understand the origin, evolution, and function of the Large HERC family, this minireview provides with an integrated overview of their structure and function and details their physiological implications. This study also highlights and discusses how dysregulation of these proteins is associated with severe human diseases such as neurological disorders and cancer. |
format | Online Article Text |
id | pubmed-6692442 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-66924422019-08-23 HERCing: Structural and Functional Relevance of the Large HERC Ubiquitin Ligases García-Cano, Jesús Martinez-Martinez, Arturo Sala-Gaston, Joan Pedrazza, Leonardo Rosa, Jose Luis Front Physiol Physiology Homologous to the E6AP carboxyl terminus (HECT) and regulator of chromosome condensation 1 (RCC1)-like domain-containing proteins (HERCs) belong to the superfamily of ubiquitin ligases. HERC proteins are divided into two subfamilies, Large and Small HERCs. Despite their similarities in terms of both structure and domains, these subfamilies are evolutionarily very distant and result from a convergence phenomenon rather than from a common origin. Large HERC genes, HERC1 and HERC2, are present in most metazoan taxa. They encode very large proteins (approximately 5,000 amino acid residues in a single polypeptide chain) that contain more than one RCC1-like domain as a structural characteristic. Accumulating evidences show that these unusually large proteins play key roles in a wide range of cellular functions which include neurodevelopment, DNA damage repair, and cell proliferation. To better understand the origin, evolution, and function of the Large HERC family, this minireview provides with an integrated overview of their structure and function and details their physiological implications. This study also highlights and discusses how dysregulation of these proteins is associated with severe human diseases such as neurological disorders and cancer. Frontiers Media S.A. 2019-08-07 /pmc/articles/PMC6692442/ /pubmed/31447701 http://dx.doi.org/10.3389/fphys.2019.01014 Text en Copyright © 2019 García-Cano, Martinez-Martinez, Sala-Gaston, Pedrazza and Rosa. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology García-Cano, Jesús Martinez-Martinez, Arturo Sala-Gaston, Joan Pedrazza, Leonardo Rosa, Jose Luis HERCing: Structural and Functional Relevance of the Large HERC Ubiquitin Ligases |
title | HERCing: Structural and Functional Relevance of the Large HERC Ubiquitin Ligases |
title_full | HERCing: Structural and Functional Relevance of the Large HERC Ubiquitin Ligases |
title_fullStr | HERCing: Structural and Functional Relevance of the Large HERC Ubiquitin Ligases |
title_full_unstemmed | HERCing: Structural and Functional Relevance of the Large HERC Ubiquitin Ligases |
title_short | HERCing: Structural and Functional Relevance of the Large HERC Ubiquitin Ligases |
title_sort | hercing: structural and functional relevance of the large herc ubiquitin ligases |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6692442/ https://www.ncbi.nlm.nih.gov/pubmed/31447701 http://dx.doi.org/10.3389/fphys.2019.01014 |
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