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CBX8 interacts with chromatin PTEN and is involved in regulating mitotic progression
OBJECTIVES: Besides its role in regulating phosphatidylinositol‐3 kinase (PI3K) signalling in the cytosol, PTEN also has a nuclear function. In this study, we attempted to understand the mechanism of chromatin PTEN in suppressing chromosomal instability during cell division. MATERIALS AND METHODS: I...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8560621/ https://www.ncbi.nlm.nih.gov/pubmed/34592789 http://dx.doi.org/10.1111/cpr.13110 |
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author | Choi, Byeong Hyeok Colon, Tania Marlyn Lee, Eunji Kou, Ziyue Dai, Wei |
author_facet | Choi, Byeong Hyeok Colon, Tania Marlyn Lee, Eunji Kou, Ziyue Dai, Wei |
author_sort | Choi, Byeong Hyeok |
collection | PubMed |
description | OBJECTIVES: Besides its role in regulating phosphatidylinositol‐3 kinase (PI3K) signalling in the cytosol, PTEN also has a nuclear function. In this study, we attempted to understand the mechanism of chromatin PTEN in suppressing chromosomal instability during cell division. MATERIALS AND METHODS: Immunocoprecipitation, ectopic expression, and deletional analyses were used to identify the physical interaction between Chromobox Homolog protein 8 (CBX8) and PTEN, as well as the functional domain(s) of PTEN mediating the interaction. Cell synchronization followed by immunoblotting was employed to study cell cycle regulation of CBX8 and the functional interaction between chromatin PTEN and CBX8. Small interfering RNAs (siRNAs) were used to study the role of PTEN and CBX8 in modulating histone epigenetic markers during the cell cycle. RESULTS: Polycomb group (PcG) proteins including CBXs function to repress gene expression in a wide range of organisms including mammals. We recently showed that PTEN interacted with CBX8, a component of Polycomb Repressing Complex 1 (PRC1), and that CBX8 co‐localized with PTEN in the nucleus. CBX8 levels were high, coinciding with its phosphorylation in mitosis. Phosphorylation of CBX8 was associated with monoubiquitinated PTEN and phosphorylated‐BubR1 on chromatin. Moreover, CBX8 played an important role in cell proliferation and mitotic progression. Significantly, downregulation of either PTEN or CBX8 induced H3K27Me3 epigenetic marker in mitotic cells. CONCLUSION: CBX8 is a new component that physically interacts with chromatin PTEN, playing an important role in regulating mitotic progression. |
format | Online Article Text |
id | pubmed-8560621 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85606212021-11-08 CBX8 interacts with chromatin PTEN and is involved in regulating mitotic progression Choi, Byeong Hyeok Colon, Tania Marlyn Lee, Eunji Kou, Ziyue Dai, Wei Cell Prolif Original Articles OBJECTIVES: Besides its role in regulating phosphatidylinositol‐3 kinase (PI3K) signalling in the cytosol, PTEN also has a nuclear function. In this study, we attempted to understand the mechanism of chromatin PTEN in suppressing chromosomal instability during cell division. MATERIALS AND METHODS: Immunocoprecipitation, ectopic expression, and deletional analyses were used to identify the physical interaction between Chromobox Homolog protein 8 (CBX8) and PTEN, as well as the functional domain(s) of PTEN mediating the interaction. Cell synchronization followed by immunoblotting was employed to study cell cycle regulation of CBX8 and the functional interaction between chromatin PTEN and CBX8. Small interfering RNAs (siRNAs) were used to study the role of PTEN and CBX8 in modulating histone epigenetic markers during the cell cycle. RESULTS: Polycomb group (PcG) proteins including CBXs function to repress gene expression in a wide range of organisms including mammals. We recently showed that PTEN interacted with CBX8, a component of Polycomb Repressing Complex 1 (PRC1), and that CBX8 co‐localized with PTEN in the nucleus. CBX8 levels were high, coinciding with its phosphorylation in mitosis. Phosphorylation of CBX8 was associated with monoubiquitinated PTEN and phosphorylated‐BubR1 on chromatin. Moreover, CBX8 played an important role in cell proliferation and mitotic progression. Significantly, downregulation of either PTEN or CBX8 induced H3K27Me3 epigenetic marker in mitotic cells. CONCLUSION: CBX8 is a new component that physically interacts with chromatin PTEN, playing an important role in regulating mitotic progression. John Wiley and Sons Inc. 2021-09-30 /pmc/articles/PMC8560621/ /pubmed/34592789 http://dx.doi.org/10.1111/cpr.13110 Text en © 2021 New York University School of Medicine. Cell Proliferation published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Choi, Byeong Hyeok Colon, Tania Marlyn Lee, Eunji Kou, Ziyue Dai, Wei CBX8 interacts with chromatin PTEN and is involved in regulating mitotic progression |
title | CBX8 interacts with chromatin PTEN and is involved in regulating mitotic progression |
title_full | CBX8 interacts with chromatin PTEN and is involved in regulating mitotic progression |
title_fullStr | CBX8 interacts with chromatin PTEN and is involved in regulating mitotic progression |
title_full_unstemmed | CBX8 interacts with chromatin PTEN and is involved in regulating mitotic progression |
title_short | CBX8 interacts with chromatin PTEN and is involved in regulating mitotic progression |
title_sort | cbx8 interacts with chromatin pten and is involved in regulating mitotic progression |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8560621/ https://www.ncbi.nlm.nih.gov/pubmed/34592789 http://dx.doi.org/10.1111/cpr.13110 |
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