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DRG2 Regulates G2/M Progression via the Cyclin B1-Cdk1 Complex
Developmentally regulated GTP-binding protein 2 (DRG2) plays an important role in cell growth. Here we explored the linkage between DRG2 and G2/M phase checkpoint function in cell cycle progression. We observed that knockdown of DRG2 in HeLa cells affected growth in a wound-healing assay, and tumori...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society for Molecular and Cellular Biology
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5050535/ https://www.ncbi.nlm.nih.gov/pubmed/27669826 http://dx.doi.org/10.14348/molcells.2016.0149 |
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author | Jang, Soo Hwa Kim, Ah-Ram Park, Neung-Hwa Park, Jeong Woo Han, In-Seob |
author_facet | Jang, Soo Hwa Kim, Ah-Ram Park, Neung-Hwa Park, Jeong Woo Han, In-Seob |
author_sort | Jang, Soo Hwa |
collection | PubMed |
description | Developmentally regulated GTP-binding protein 2 (DRG2) plays an important role in cell growth. Here we explored the linkage between DRG2 and G2/M phase checkpoint function in cell cycle progression. We observed that knockdown of DRG2 in HeLa cells affected growth in a wound-healing assay, and tumorigenicity in nude mice xenografts. Flow cytometry assays and [(3)H] incorporation assays indicated that G2/M phase arrest was responsible for the decreased proliferation of these cells. Knockdown of DRG2 elicited down-regulation of the major mitotic promoting factor, the cyclin B1/Cdk1 complex, but up-regulation of the cell cycle arresting proteins, Wee1, Myt1, and p21. These findings identify a novel role of DRG2 in G2/M progression. |
format | Online Article Text |
id | pubmed-5050535 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Korean Society for Molecular and Cellular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-50505352016-10-07 DRG2 Regulates G2/M Progression via the Cyclin B1-Cdk1 Complex Jang, Soo Hwa Kim, Ah-Ram Park, Neung-Hwa Park, Jeong Woo Han, In-Seob Mol Cells Article Developmentally regulated GTP-binding protein 2 (DRG2) plays an important role in cell growth. Here we explored the linkage between DRG2 and G2/M phase checkpoint function in cell cycle progression. We observed that knockdown of DRG2 in HeLa cells affected growth in a wound-healing assay, and tumorigenicity in nude mice xenografts. Flow cytometry assays and [(3)H] incorporation assays indicated that G2/M phase arrest was responsible for the decreased proliferation of these cells. Knockdown of DRG2 elicited down-regulation of the major mitotic promoting factor, the cyclin B1/Cdk1 complex, but up-regulation of the cell cycle arresting proteins, Wee1, Myt1, and p21. These findings identify a novel role of DRG2 in G2/M progression. Korean Society for Molecular and Cellular Biology 2016-09 2016-09-27 /pmc/articles/PMC5050535/ /pubmed/27669826 http://dx.doi.org/10.14348/molcells.2016.0149 Text en © The Korean Society for Molecular and Cellular Biology. All rights reserved. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/. |
spellingShingle | Article Jang, Soo Hwa Kim, Ah-Ram Park, Neung-Hwa Park, Jeong Woo Han, In-Seob DRG2 Regulates G2/M Progression via the Cyclin B1-Cdk1 Complex |
title | DRG2 Regulates G2/M Progression via the Cyclin B1-Cdk1 Complex |
title_full | DRG2 Regulates G2/M Progression via the Cyclin B1-Cdk1 Complex |
title_fullStr | DRG2 Regulates G2/M Progression via the Cyclin B1-Cdk1 Complex |
title_full_unstemmed | DRG2 Regulates G2/M Progression via the Cyclin B1-Cdk1 Complex |
title_short | DRG2 Regulates G2/M Progression via the Cyclin B1-Cdk1 Complex |
title_sort | drg2 regulates g2/m progression via the cyclin b1-cdk1 complex |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5050535/ https://www.ncbi.nlm.nih.gov/pubmed/27669826 http://dx.doi.org/10.14348/molcells.2016.0149 |
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