TSPYL2 is important for G1 checkpoint maintenance upon DNA damage
Nucleosome assembly proteins play important roles in chromatin remodeling, which determines gene expression, cell proliferation and terminal differentiation. Testis specific protein, Y-encoded-like 2 (TSPYL2) is a nucleosome assembly protein expressed in neuronal precursors and mature neurons. Previ...
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description | Nucleosome assembly proteins play important roles in chromatin remodeling, which determines gene expression, cell proliferation and terminal differentiation. Testis specific protein, Y-encoded-like 2 (TSPYL2) is a nucleosome assembly protein expressed in neuronal precursors and mature neurons. Previous studies have shown that TSPYL2 binds cyclin B and inhibits cell proliferation in cultured cells suggesting a role in cell cycle regulation. To investigate the physiological significance of TSPYL2 in the control of cell cycle, we generated mice with targeted disruption of Tspyl2. These mutant mice appear grossly normal, have normal life span and do not exhibit increased tumor incidence. To define the role of TSPYL2 in DNA repair, checkpoint arrest and apoptosis, primary embryonic fibroblasts and thymocytes from Tspyl2 deficient mice were isolated and examined under unperturbed and stressed conditions. We show that mutant fibroblasts are impaired in G1 arrest under the situation of DNA damage induced by gamma irradiation. This is mainly attributed to the defective activation of p21 transcription despite proper p53 protein accumulation, suggesting that TSPYL2 is additionally required for p21 induction. TSPYL2 serves a biological role in maintaining the G1 checkpoint under stress condition. |
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Testis specific protein, Y-encoded-like 2 (TSPYL2) is a nucleosome assembly protein expressed in neuronal precursors and mature neurons. Previous studies have shown that TSPYL2 binds cyclin B and inhibits cell proliferation in cultured cells suggesting a role in cell cycle regulation. To investigate the physiological significance of TSPYL2 in the control of cell cycle, we generated mice with targeted disruption of Tspyl2. These mutant mice appear grossly normal, have normal life span and do not exhibit increased tumor incidence. To define the role of TSPYL2 in DNA repair, checkpoint arrest and apoptosis, primary embryonic fibroblasts and thymocytes from Tspyl2 deficient mice were isolated and examined under unperturbed and stressed conditions. We show that mutant fibroblasts are impaired in G1 arrest under the situation of DNA damage induced by gamma irradiation. This is mainly attributed to the defective activation of p21 transcription despite proper p53 protein accumulation, suggesting that TSPYL2 is additionally required for p21 induction. TSPYL2 serves a biological role in maintaining the G1 checkpoint under stress condition.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0021602</identifier><identifier>PMID: 21738728</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Animals ; Apoptosis ; Apoptosis - genetics ; Apoptosis - physiology ; Assembly ; Biology ; Blotting, Northern ; Blotting, Western ; Cell cycle ; Cell Cycle - genetics ; Cell Cycle - physiology ; Cell Cycle Proteins - genetics ; Cell Cycle Proteins - metabolism ; Cell growth ; Cell proliferation ; Cells, Cultured ; Chromatin ; Chromatin remodeling ; Cyclin B ; Cyclin-dependent kinase inhibitor p21 ; Deoxyribonucleic acid ; Disruption ; DNA ; DNA damage ; DNA Damage - genetics ; DNA Damage - physiology ; DNA repair ; Embryo fibroblasts ; Embryos ; Fibroblasts ; Flow Cytometry ; G1 Phase - genetics ; G1 Phase - physiology ; Gamma irradiation ; Gamma rays ; Gene expression ; GTP-binding protein ; Immunohistochemistry ; Ionizing radiation ; Irradiation ; Kinases ; Life span ; Mice ; Mice, Knockout ; Neural stem cells ; Neurons ; p53 Protein ; Physiological aspects ; Proteins ; Radiation damage ; Rodents ; Thymocytes ; Transcription activation ; Tumor proteins</subject><ispartof>PloS one, 2011-06, Vol.6 (6), p.e21602-e21602</ispartof><rights>COPYRIGHT 2011 Public Library of Science</rights><rights>2011 Tao et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Tao et al. 2011</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c757t-4433b75d2012734be03dff4a0cfaee01e401ff2fc8a701cc6e0e44c5680a38813</citedby><cites>FETCH-LOGICAL-c757t-4433b75d2012734be03dff4a0cfaee01e401ff2fc8a701cc6e0e44c5680a38813</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3124543/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3124543/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2095,2914,23846,27903,27904,53770,53772,79347,79348</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21738728$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Borgmann, Kerstin</contributor><creatorcontrib>Tao, Kin Pong</creatorcontrib><creatorcontrib>Fong, Sze Wan</creatorcontrib><creatorcontrib>Lu, Zhihong</creatorcontrib><creatorcontrib>Ching, Yick Pang</creatorcontrib><creatorcontrib>Chan, Kin Wang</creatorcontrib><creatorcontrib>Chan, Siu Yuen</creatorcontrib><title>TSPYL2 is important for G1 checkpoint maintenance upon DNA damage</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Nucleosome assembly proteins play important roles in chromatin remodeling, which determines gene expression, cell proliferation and terminal differentiation. Testis specific protein, Y-encoded-like 2 (TSPYL2) is a nucleosome assembly protein expressed in neuronal precursors and mature neurons. Previous studies have shown that TSPYL2 binds cyclin B and inhibits cell proliferation in cultured cells suggesting a role in cell cycle regulation. To investigate the physiological significance of TSPYL2 in the control of cell cycle, we generated mice with targeted disruption of Tspyl2. These mutant mice appear grossly normal, have normal life span and do not exhibit increased tumor incidence. To define the role of TSPYL2 in DNA repair, checkpoint arrest and apoptosis, primary embryonic fibroblasts and thymocytes from Tspyl2 deficient mice were isolated and examined under unperturbed and stressed conditions. We show that mutant fibroblasts are impaired in G1 arrest under the situation of DNA damage induced by gamma irradiation. This is mainly attributed to the defective activation of p21 transcription despite proper p53 protein accumulation, suggesting that TSPYL2 is additionally required for p21 induction. TSPYL2 serves a biological role in maintaining the G1 checkpoint under stress condition.</description><subject>Animals</subject><subject>Apoptosis</subject><subject>Apoptosis - genetics</subject><subject>Apoptosis - physiology</subject><subject>Assembly</subject><subject>Biology</subject><subject>Blotting, Northern</subject><subject>Blotting, Western</subject><subject>Cell cycle</subject><subject>Cell Cycle - genetics</subject><subject>Cell Cycle - physiology</subject><subject>Cell Cycle Proteins - genetics</subject><subject>Cell Cycle Proteins - metabolism</subject><subject>Cell growth</subject><subject>Cell proliferation</subject><subject>Cells, Cultured</subject><subject>Chromatin</subject><subject>Chromatin remodeling</subject><subject>Cyclin B</subject><subject>Cyclin-dependent kinase inhibitor p21</subject><subject>Deoxyribonucleic acid</subject><subject>Disruption</subject><subject>DNA</subject><subject>DNA damage</subject><subject>DNA Damage - genetics</subject><subject>DNA Damage - physiology</subject><subject>DNA repair</subject><subject>Embryo fibroblasts</subject><subject>Embryos</subject><subject>Fibroblasts</subject><subject>Flow Cytometry</subject><subject>G1 Phase - genetics</subject><subject>G1 Phase - physiology</subject><subject>Gamma irradiation</subject><subject>Gamma rays</subject><subject>Gene expression</subject><subject>GTP-binding protein</subject><subject>Immunohistochemistry</subject><subject>Ionizing radiation</subject><subject>Irradiation</subject><subject>Kinases</subject><subject>Life span</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>Neural stem cells</subject><subject>Neurons</subject><subject>p53 Protein</subject><subject>Physiological aspects</subject><subject>Proteins</subject><subject>Radiation damage</subject><subject>Rodents</subject><subject>Thymocytes</subject><subject>Transcription activation</subject><subject>Tumor 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is important for G1 checkpoint maintenance upon DNA damage</title><author>Tao, Kin Pong ; Fong, Sze Wan ; Lu, Zhihong ; Ching, Yick Pang ; Chan, Kin Wang ; Chan, Siu Yuen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c757t-4433b75d2012734be03dff4a0cfaee01e401ff2fc8a701cc6e0e44c5680a38813</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animals</topic><topic>Apoptosis</topic><topic>Apoptosis - genetics</topic><topic>Apoptosis - physiology</topic><topic>Assembly</topic><topic>Biology</topic><topic>Blotting, Northern</topic><topic>Blotting, Western</topic><topic>Cell cycle</topic><topic>Cell Cycle - genetics</topic><topic>Cell Cycle - physiology</topic><topic>Cell Cycle Proteins - genetics</topic><topic>Cell Cycle Proteins - metabolism</topic><topic>Cell growth</topic><topic>Cell proliferation</topic><topic>Cells, Cultured</topic><topic>Chromatin</topic><topic>Chromatin 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tao, Kin Pong</au><au>Fong, Sze Wan</au><au>Lu, Zhihong</au><au>Ching, Yick Pang</au><au>Chan, Kin Wang</au><au>Chan, Siu Yuen</au><au>Borgmann, Kerstin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>TSPYL2 is important for G1 checkpoint maintenance upon DNA damage</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2011-06-27</date><risdate>2011</risdate><volume>6</volume><issue>6</issue><spage>e21602</spage><epage>e21602</epage><pages>e21602-e21602</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Nucleosome assembly proteins play important roles in chromatin remodeling, which determines gene expression, cell proliferation and terminal differentiation. Testis specific protein, Y-encoded-like 2 (TSPYL2) is a nucleosome assembly protein expressed in neuronal precursors and mature neurons. Previous studies have shown that TSPYL2 binds cyclin B and inhibits cell proliferation in cultured cells suggesting a role in cell cycle regulation. To investigate the physiological significance of TSPYL2 in the control of cell cycle, we generated mice with targeted disruption of Tspyl2. These mutant mice appear grossly normal, have normal life span and do not exhibit increased tumor incidence. To define the role of TSPYL2 in DNA repair, checkpoint arrest and apoptosis, primary embryonic fibroblasts and thymocytes from Tspyl2 deficient mice were isolated and examined under unperturbed and stressed conditions. We show that mutant fibroblasts are impaired in G1 arrest under the situation of DNA damage induced by gamma irradiation. This is mainly attributed to the defective activation of p21 transcription despite proper p53 protein accumulation, suggesting that TSPYL2 is additionally required for p21 induction. TSPYL2 serves a biological role in maintaining the G1 checkpoint under stress condition.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>21738728</pmid><doi>10.1371/journal.pone.0021602</doi><tpages>e21602</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Apoptosis Apoptosis - genetics Apoptosis - physiology Assembly Biology Blotting, Northern Blotting, Western Cell cycle Cell Cycle - genetics Cell Cycle - physiology Cell Cycle Proteins - genetics Cell Cycle Proteins - metabolism Cell growth Cell proliferation Cells, Cultured Chromatin Chromatin remodeling Cyclin B Cyclin-dependent kinase inhibitor p21 Deoxyribonucleic acid Disruption DNA DNA damage DNA Damage - genetics DNA Damage - physiology DNA repair Embryo fibroblasts Embryos Fibroblasts Flow Cytometry G1 Phase - genetics G1 Phase - physiology Gamma irradiation Gamma rays Gene expression GTP-binding protein Immunohistochemistry Ionizing radiation Irradiation Kinases Life span Mice Mice, Knockout Neural stem cells Neurons p53 Protein Physiological aspects Proteins Radiation damage Rodents Thymocytes Transcription activation Tumor proteins |
title | TSPYL2 is important for G1 checkpoint maintenance upon DNA damage |
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