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Growth arrest–specific 2 protein family: Structure and function

Members of the growth arrest–specific 2 (GAS2) protein family consist of a putative actin‐binding (CH) domain and a microtubule‐binding (GAR) domain and are considered miniversions of spectraplakins. There are four members in the GAS2 family, viz. GAS2, GAS2L1, GAS2L2 and GAS2L3. Although GAS2 is de...

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Autores principales: Zhang, Nan, Zhao, Chunyan, Zhang, Xinxin, Cui, Xiaoteng, Zhao, Yan, Yang, Jie, Gao, Xingjie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7791176/
https://www.ncbi.nlm.nih.gov/pubmed/33103301
http://dx.doi.org/10.1111/cpr.12934
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author Zhang, Nan
Zhao, Chunyan
Zhang, Xinxin
Cui, Xiaoteng
Zhao, Yan
Yang, Jie
Gao, Xingjie
author_facet Zhang, Nan
Zhao, Chunyan
Zhang, Xinxin
Cui, Xiaoteng
Zhao, Yan
Yang, Jie
Gao, Xingjie
author_sort Zhang, Nan
collection PubMed
description Members of the growth arrest–specific 2 (GAS2) protein family consist of a putative actin‐binding (CH) domain and a microtubule‐binding (GAR) domain and are considered miniversions of spectraplakins. There are four members in the GAS2 family, viz. GAS2, GAS2L1, GAS2L2 and GAS2L3. Although GAS2 is defined as a family of growth arrest–specific proteins, the significant differences in the expression patterns, interaction characteristics and biological issues or diseases among the different GAS2 family members have not been systemically reviewed to date. Therefore, we summarized the available evidence on the structures and functions of GAS2 family members. This review facilitates a comprehensive molecular understanding of the involvement of the GAS2 family members in an array of biological processes, including cytoskeleton reorganization, cell cycle, apoptosis and cancer development.
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spelling pubmed-77911762021-01-11 Growth arrest–specific 2 protein family: Structure and function Zhang, Nan Zhao, Chunyan Zhang, Xinxin Cui, Xiaoteng Zhao, Yan Yang, Jie Gao, Xingjie Cell Prolif Reviews Members of the growth arrest–specific 2 (GAS2) protein family consist of a putative actin‐binding (CH) domain and a microtubule‐binding (GAR) domain and are considered miniversions of spectraplakins. There are four members in the GAS2 family, viz. GAS2, GAS2L1, GAS2L2 and GAS2L3. Although GAS2 is defined as a family of growth arrest–specific proteins, the significant differences in the expression patterns, interaction characteristics and biological issues or diseases among the different GAS2 family members have not been systemically reviewed to date. Therefore, we summarized the available evidence on the structures and functions of GAS2 family members. This review facilitates a comprehensive molecular understanding of the involvement of the GAS2 family members in an array of biological processes, including cytoskeleton reorganization, cell cycle, apoptosis and cancer development. John Wiley and Sons Inc. 2020-10-25 /pmc/articles/PMC7791176/ /pubmed/33103301 http://dx.doi.org/10.1111/cpr.12934 Text en © 2020 The Authors. Cell Proliferation Published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reviews
Zhang, Nan
Zhao, Chunyan
Zhang, Xinxin
Cui, Xiaoteng
Zhao, Yan
Yang, Jie
Gao, Xingjie
Growth arrest–specific 2 protein family: Structure and function
title Growth arrest–specific 2 protein family: Structure and function
title_full Growth arrest–specific 2 protein family: Structure and function
title_fullStr Growth arrest–specific 2 protein family: Structure and function
title_full_unstemmed Growth arrest–specific 2 protein family: Structure and function
title_short Growth arrest–specific 2 protein family: Structure and function
title_sort growth arrest–specific 2 protein family: structure and function
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7791176/
https://www.ncbi.nlm.nih.gov/pubmed/33103301
http://dx.doi.org/10.1111/cpr.12934
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