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Overexpression of DA41 in v‐Ha‐ras‐3Y1 Cells Causes Growth Suppression

We have recently found that DA41 exhibits marked homology with mouse PLIC‐1, PLIC‐2, frog XDRP1 and yeast DSK2. XDRP1 has been shown to be associated with cyclin A, and blocks cell division of frog embryo. In the present study, we examined the biological role(s) of DA41 in mammalian cells by overexp...

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Detalles Bibliográficos
Autores principales: Ozaki, Toshinori, Nakamura, Yohko, Hanaoka, Eiji, Nakagawara, Akira, Sakiyama, Shigeru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5926252/
https://www.ncbi.nlm.nih.gov/pubmed/11050468
http://dx.doi.org/10.1111/j.1349-7006.2000.tb00875.x
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author Ozaki, Toshinori
Nakamura, Yohko
Hanaoka, Eiji
Nakagawara, Akira
Sakiyama, Shigeru
author_facet Ozaki, Toshinori
Nakamura, Yohko
Hanaoka, Eiji
Nakagawara, Akira
Sakiyama, Shigeru
author_sort Ozaki, Toshinori
collection PubMed
description We have recently found that DA41 exhibits marked homology with mouse PLIC‐1, PLIC‐2, frog XDRP1 and yeast DSK2. XDRP1 has been shown to be associated with cyclin A, and blocks cell division of frog embryo. In the present study, we examined the biological role(s) of DA41 in mammalian cells by overexpressing it in v‐Ha‐ras‐transformed 3Y1 cells (ras‐3Y1). Transfectants which expressed a high level of DA41 mRNA exhibited a decrease in growth rate, a reduction in saturation density, and a suppression of colony formation in soft agar medium. To clarify the molecular mechanism(s) by which DA41 affects cell growth, the effect of DA41 expression on the levels of various cell cycle‐regulatory proteins was examined. The forced expression of DA41 gene resulted in a remarkable reduction in CDK2 activity, while the amount of CDK2 did not change. These observations indicate that DA41 is involved in cell cycle regulation in ras‐3Y1 cells.
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spelling pubmed-59262522018-05-11 Overexpression of DA41 in v‐Ha‐ras‐3Y1 Cells Causes Growth Suppression Ozaki, Toshinori Nakamura, Yohko Hanaoka, Eiji Nakagawara, Akira Sakiyama, Shigeru Jpn J Cancer Res Rapid Communication We have recently found that DA41 exhibits marked homology with mouse PLIC‐1, PLIC‐2, frog XDRP1 and yeast DSK2. XDRP1 has been shown to be associated with cyclin A, and blocks cell division of frog embryo. In the present study, we examined the biological role(s) of DA41 in mammalian cells by overexpressing it in v‐Ha‐ras‐transformed 3Y1 cells (ras‐3Y1). Transfectants which expressed a high level of DA41 mRNA exhibited a decrease in growth rate, a reduction in saturation density, and a suppression of colony formation in soft agar medium. To clarify the molecular mechanism(s) by which DA41 affects cell growth, the effect of DA41 expression on the levels of various cell cycle‐regulatory proteins was examined. The forced expression of DA41 gene resulted in a remarkable reduction in CDK2 activity, while the amount of CDK2 did not change. These observations indicate that DA41 is involved in cell cycle regulation in ras‐3Y1 cells. Blackwell Publishing Ltd 2000-10 /pmc/articles/PMC5926252/ /pubmed/11050468 http://dx.doi.org/10.1111/j.1349-7006.2000.tb00875.x Text en
spellingShingle Rapid Communication
Ozaki, Toshinori
Nakamura, Yohko
Hanaoka, Eiji
Nakagawara, Akira
Sakiyama, Shigeru
Overexpression of DA41 in v‐Ha‐ras‐3Y1 Cells Causes Growth Suppression
title Overexpression of DA41 in v‐Ha‐ras‐3Y1 Cells Causes Growth Suppression
title_full Overexpression of DA41 in v‐Ha‐ras‐3Y1 Cells Causes Growth Suppression
title_fullStr Overexpression of DA41 in v‐Ha‐ras‐3Y1 Cells Causes Growth Suppression
title_full_unstemmed Overexpression of DA41 in v‐Ha‐ras‐3Y1 Cells Causes Growth Suppression
title_short Overexpression of DA41 in v‐Ha‐ras‐3Y1 Cells Causes Growth Suppression
title_sort overexpression of da41 in v‐ha‐ras‐3y1 cells causes growth suppression
topic Rapid Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5926252/
https://www.ncbi.nlm.nih.gov/pubmed/11050468
http://dx.doi.org/10.1111/j.1349-7006.2000.tb00875.x
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