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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Veröffentlicht in:PloS one 2011-06, Vol.6 (6), p.e21602-e21602
Hauptverfasser: Tao, Kin Pong, Fong, Sze Wan, Lu, Zhihong, Ching, Yick Pang, Chan, Kin Wang, Chan, Siu Yuen
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container_issue 6
container_start_page e21602
container_title PloS one
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creator Tao, Kin Pong
Fong, Sze Wan
Lu, Zhihong
Ching, Yick Pang
Chan, Kin Wang
Chan, Siu Yuen
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.
doi_str_mv 10.1371/journal.pone.0021602
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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. 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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. 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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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