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The Roles of SPOP in DNA Damage Response and DNA Replication
Speckle-type BTB/POZ protein (SPOP) is a substrate recognition receptor of the cullin-3 (CUL3)/RING type ubiquitin E3 complex. To date, approximately 30 proteins have been identified as ubiquitinated substrates of the CUL3/SPOP complex. Pathologically, missense mutations in the substrate-binding dom...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7582541/ https://www.ncbi.nlm.nih.gov/pubmed/33023230 http://dx.doi.org/10.3390/ijms21197293 |
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author | Maekawa, Masashi Higashiyama, Shigeki |
author_facet | Maekawa, Masashi Higashiyama, Shigeki |
author_sort | Maekawa, Masashi |
collection | PubMed |
description | Speckle-type BTB/POZ protein (SPOP) is a substrate recognition receptor of the cullin-3 (CUL3)/RING type ubiquitin E3 complex. To date, approximately 30 proteins have been identified as ubiquitinated substrates of the CUL3/SPOP complex. Pathologically, missense mutations in the substrate-binding domain of SPOP have been found in prostate and endometrial cancers. Prostate and endometrial cancer-associated SPOP mutations lose and increase substrate-binding ability, respectively. Expression of these SPOP mutants, thus, causes aberrant turnovers of the substrate proteins, leading to tumor formation. Although the molecular properties of SPOP and its cancer-associated mutants have been intensively elucidated, their cellular functions remain unclear. Recently, a number of studies have uncovered the critical role of SPOP and its mutants in DNA damage response and DNA replication. In this review article, we summarize the physiological functions of SPOP as a “gatekeeper” of genome stability. |
format | Online Article Text |
id | pubmed-7582541 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-75825412020-10-29 The Roles of SPOP in DNA Damage Response and DNA Replication Maekawa, Masashi Higashiyama, Shigeki Int J Mol Sci Review Speckle-type BTB/POZ protein (SPOP) is a substrate recognition receptor of the cullin-3 (CUL3)/RING type ubiquitin E3 complex. To date, approximately 30 proteins have been identified as ubiquitinated substrates of the CUL3/SPOP complex. Pathologically, missense mutations in the substrate-binding domain of SPOP have been found in prostate and endometrial cancers. Prostate and endometrial cancer-associated SPOP mutations lose and increase substrate-binding ability, respectively. Expression of these SPOP mutants, thus, causes aberrant turnovers of the substrate proteins, leading to tumor formation. Although the molecular properties of SPOP and its cancer-associated mutants have been intensively elucidated, their cellular functions remain unclear. Recently, a number of studies have uncovered the critical role of SPOP and its mutants in DNA damage response and DNA replication. In this review article, we summarize the physiological functions of SPOP as a “gatekeeper” of genome stability. MDPI 2020-10-02 /pmc/articles/PMC7582541/ /pubmed/33023230 http://dx.doi.org/10.3390/ijms21197293 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Maekawa, Masashi Higashiyama, Shigeki The Roles of SPOP in DNA Damage Response and DNA Replication |
title | The Roles of SPOP in DNA Damage Response and DNA Replication |
title_full | The Roles of SPOP in DNA Damage Response and DNA Replication |
title_fullStr | The Roles of SPOP in DNA Damage Response and DNA Replication |
title_full_unstemmed | The Roles of SPOP in DNA Damage Response and DNA Replication |
title_short | The Roles of SPOP in DNA Damage Response and DNA Replication |
title_sort | roles of spop in dna damage response and dna replication |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7582541/ https://www.ncbi.nlm.nih.gov/pubmed/33023230 http://dx.doi.org/10.3390/ijms21197293 |
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