help button home button
AJRCMB
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

Published ahead of print on April 5, 2007, doi:10.1165/rcmb.2005-0345RC
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
2005-0345RCv1
37/1/9    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Yuan, X.
Right arrow Articles by Cong, Y.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Yuan, X.
Right arrow Articles by Cong, Y.
American Journal of Respiratory Cell and Molecular Biology. Vol. 37, pp. 9-19, 2007
© 2007 American Thoracic Society
DOI: 10.1165/rcmb.2005-0345RC


Rapid Communications

G1 Phase Cell Cycle Arrest Induced by SARS-CoV 3a Protein via the Cyclin D3/pRb Pathway

Xiaoling Yuan*, Zhenyu Yao*, Jie Wu, Yusen Zhou, Yajun Shan, Bo Dong, Zhenhu Zhao, Ping Hua, Jiapei Chen and Yuwen Cong

Department of Pathophysiology, Beijing Institute of Radiation Medicine, and State Key Laboratory of Pathogen and Biosecurity, Department of Pathogenic Molecular Biology, Beijing Institute of Microbiology and Epidemiology, Beijing, China

Correspondence and requests for reprints should be addressed to Yuwen Cong, Ph.D., Department of Pathophysiology, Beijing Institute of Radiation Medicine, No. 27 Taiping Road, Beijing, 100850, China. E-mail: congyw{at}nic.bmi.ac.cn

SARS-CoV 3a is a structural protein, mainly localizing to Golgi apparatus and co-localizing with SARS-CoV M in co-transfected cells. Here we observed that transient expression of 3a inhibited cell growth and prevented 5-bromodeoxyuridine incorporation, suggesting that 3a deregulated cell cycle progression. Cell cycle analysis demonstrated that 3a expression was associated with blockage of cell cycle progression at G1 phase in HEK 293, COS-7, and Vero cells 24–60 h after transfection. Mutation analysis of 3a revealed that C-terminal region (176 aa ~ 274 aa), including a potential calcium ATPase motif, was essential for induction of cell cycle arrest. Topological analysis showed that 3a predominantly located in Golgi apparatus, with its N-terminus residing in the lumen (Nlum) and C-terminus in the cytosol (Ccyt). Analyzing the cellular proteins involving in regulation of cell cycle progression, we demonstrated that 3a expression was correlated with a significant reduction of cyclin D3 level and phosphorylation of retinoblastoma (Rb) protein at Ser-795 and Ser-809/811, not with the expression of cyclin D1, D2, cdk4, and cdk6 in 293 cells. Increases in p53 phosphorylation on Ser-15 were observed in both SARS-CoV M and 3a transfected cells, suggesting that it might not correlate with the 3a-induced G0/G1 phase arrest. The reduction of cyclin D3 level and phosphorylation of Rb were further confirmed in SARS-CoV infected Vero cells. These results indicate that SARS-CoV 3a protein, through limiting the expression of cyclin D3, may inhibit Rb phosphorylation, which in turn leads to a block in the G1 phase of the cell cycle and an inhibition of cell proliferation.

Key Words: SARS-CoV 3a • growth inhibition • G1 phase cell cycle arrest • cyclin D3 • pRb


CLINICAL RELEVANCE

Our results suggested that the SARS-CoV 3a protein plays important roles in the SARS-CoV life cycle and virus-induced pathogenesis.

 






HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Proc. Am. Thorac. Soc. Am. J. Respir. Crit. Care Med.
Copyright © 2007 American Thoracic Society.
  ATS Best of the Web