Volume 37, Issue 11 pp. 767-772

Function of c-Fos-like and c-Jun-like Proteins on Trichostatin A-induced G2/M Arrest in Physarum polycephalum

Xiao-Xue LI

Xiao-Xue LI

Institute of Genetics and Cytology, Northeast Normal University, Changchun 130024, China

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Jun LU

Jun LU

Institute of Genetics and Cytology, Northeast Normal University, Changchun 130024, China

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Yan-Mei ZHAO

Yan-Mei ZHAO

Institute of Genetics and Cytology, Northeast Normal University, Changchun 130024, China

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Bai-Qu HUANG

Corresponding Author

Bai-Qu HUANG

Institute of Genetics and Cytology, Northeast Normal University, Changchun 130024, China

*Tel, 86-431-5099768; Fax, 86-431-5681833; E-mail: [email protected]Search for more papers by this author
First published: 15 November 2005
Citations: 1

The work was supported by the grants from the National Natural Science Foundation of China (30571698), the Major State Basic Research Project of China (2005CB522404) and the Young Teacher Foundation of Northeast Normal University (111494025)

Abstract

Abstract The homologs of transcription factors c-Fos and c-Jun have been detected in slime mold Physarum polycephalum during progression of the synchronous cell cycle. Here we demonstrated that c-Fos-like and c-Jun-like proteins participated in G2/M transition by the regulation of the level of Cyclin B1 protein in P. polycephalum. The study of antibody neutralization revealed that interruption of the functions of c-Fos-like and c-Jun-like proteins resulted in G2/M transition arrest, implicating their functional roles in cell cycle control. When G2/M transition was blocked by histone deacetylase inhibitor trichostatin A, changes in c-Fos- and c-Jun-like protein levels, and hyperacetylation of c-Jun-like protein, were observed. The data suggest that in P. polycephalum, c-Fos- and c-Jun-like proteins may be the key factors in the regulation of histone acetylation-related G2/M transition, involving the coordinated expression and hyperacetylation of these proteins.

Edited by Ming-Hua XU

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