Protein profiles of the Chinese hamster ovary cells in the resting and proliferating stages. Naryzhny, S. & Lee, H. Electrophoresis, 22(9):1764-1775, 2001. cited By 39
Protein profiles of the Chinese hamster ovary cells in the resting and proliferating stages [link]Paper  doi  abstract   bibtex   
Identification and characterization of the proteins that regulate the transition from the resting stage (G0) through G1 to S phase of the cell cycle are of central importance to understand the control of cell proliferation and chromosome replication. Unlike in lower organisms, where relatively small numbers of key factors are involved in this process, the factors involved in the same control mechanisms in mammalian systems are much more complex. Furthermore, accumulating lines of evidence now suggest that the nuclear matrix and chromatin organization also play an essential role for the cell cycle control in mammalian cells. To gain a better understanding of the overall dynamics and changes of the protein factors in the context of matrix/chromatin organization, we examined the protein profiles of the Chinese hamster ovary (CHO) cells in different cell cycle compartments. The methods used in this study included subcellular fractionations (cytosol, nuclear extraction, chromatin, and nuclear matrix), two-dimensional polyacrylamide gel electrophoresis (2-D PAGE), silver staining, and immunoblotting. As expected, significant changes of protein profiles were observed when cells entered into proliferating stages from G0. Among approximately 1200 protein spots analyzed by 2-D PAGE, at least 12 showed marked increase or decrease at this transitional period. Further cell-cycle progression from G1 to S phase showed less dramatic changes of overall protein protile. However, the profile of certain proteins showed rather dramatic changes of their subcellular localization during this transitional period. In particular, the levels of proliferating cell nuclear antigen (PCNA) in the nuclear matrix and chromatin dramatically increased in mid-G1 and in the beginning of S phase, respectively, while the overall PCNA level was relatively constant throughout the cell cycle. © Wiley-VCH Verlag GmbH, 2001.
@ARTICLE{Naryzhny20011764,
author={Naryzhny, S.N. and Lee, H.},
title={Protein profiles of the Chinese hamster ovary cells in the resting and proliferating stages},
journal={Electrophoresis},
year={2001},
volume={22},
number={9},
pages={1764-1775},
doi={10.1002/1522-2683(200105)22:9<1764::AID-ELPS1764>3.0.CO;2-V},
note={cited By 39},
url={https://www.scopus.com/inward/record.uri?eid=2-s2.0-70449624651&doi=10.1002%2f1522-2683%28200105%2922%3a9%3c1764%3a%3aAID-ELPS1764%3e3.0.CO%3b2-V&partnerID=40&md5=6af15afeb09e99e3d258565aff4a1ecf},
affiliation={Department of Research, Northeastern Ontario Regional Cancer Centre, 41 Ramsey Lake Road, Sudbury, ON P3E 5J1, Canada},
abstract={Identification and characterization of the proteins that regulate the transition from the resting stage (G0) through G1 to S phase of the cell cycle are of central importance to understand the control of cell proliferation and chromosome replication. Unlike in lower organisms, where relatively small numbers of key factors are involved in this process, the factors involved in the same control mechanisms in mammalian systems are much more complex. Furthermore, accumulating lines of evidence now suggest that the nuclear matrix and chromatin organization also play an essential role for the cell cycle control in mammalian cells. To gain a better understanding of the overall dynamics and changes of the protein factors in the context of matrix/chromatin organization, we examined the protein profiles of the Chinese hamster ovary (CHO) cells in different cell cycle compartments. The methods used in this study included subcellular fractionations (cytosol, nuclear extraction, chromatin, and nuclear matrix), two-dimensional polyacrylamide gel electrophoresis (2-D PAGE), silver staining, and immunoblotting. As expected, significant changes of protein profiles were observed when cells entered into proliferating stages from G0. Among approximately 1200 protein spots analyzed by 2-D PAGE, at least 12 showed marked increase or decrease at this transitional period. Further cell-cycle progression from G1 to S phase showed less dramatic changes of overall protein protile. However, the profile of certain proteins showed rather dramatic changes of their subcellular localization during this transitional period. In particular, the levels of proliferating cell nuclear antigen (PCNA) in the nuclear matrix and chromatin dramatically increased in mid-G1 and in the beginning of S phase, respectively, while the overall PCNA level was relatively constant throughout the cell cycle. © Wiley-VCH Verlag GmbH, 2001.},
author_keywords={Cell proliferation;  Chinese hamster ovary cells;  Proliferating cell nuclear antigen;  Subcellular fractionation;  Two-dimensional polyacrylamide gel electrophoresis},
correspondence_address1={Lee, H.; Department of Research, Northeastern Ontario Regional Cancer Centre, 41 Ramsey Lake Road, Sudbury, ON P3E 5J1, Canada; email: hlee@neorcc.on.ca},
issn={01730835},
coden={ELCTD},
language={English},
abbrev_source_title={Electrophoresis},
document_type={Article},
source={Scopus},
}

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