n-butyrate mediated inhibition of papovavirus DNA replication in vivo and in cell culture:: A mechanistic approach

被引:2
|
作者
Shadan, FF
Villarreal, LP
机构
[1] Scripps Clin, Dept Internal Med, La Jolla, CA 92037 USA
[2] Univ Calif Irvine, Dept Mol Biol & Biochem, Irvine, CA 92717 USA
基金
美国国家卫生研究院;
关键词
papillomavirus; polyomavirus; DNA polymerase; proliferating cell nuclear antigen; replication; n-butyrate;
D O I
10.1023/A:1008184326950
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
n-Butyrate, an inhibitor of G(1)-to-S transition inhibits papovavirus DNA replication in cell culture. To explore the efficacy of n-butyrate in vivo and to better understand its mechanism, we studied the effect of n-butyrate on viral DNA replication in mice acutely infected with polyomavirus and in the papovavirus-infected cells in culture. Newborn mice treated with n-butyrate stop growing and become runted. When infected with polyomavirus, these mice show a strong overall inhibition of viral DNA. However, a notable exception to this was the continued viral DNA replication in the differentiated mouse keratinocytes and renal epithelial cells as determined by in situ hybridization. n-Butyrate significantly inhibited viral DNA replication in the cultured IDL cells, and in polyomavirus-infected C2C12 myoblasts based on Southern blot analysis and in situ hybridization. DNA polymerase alpha (but not DNA polymerase beta) and the characteristic nuclear expression of PCNA were both inhibited in the n-butyrate treated IDL and C2C12 cells. n-Butyrate, therefore, inhibited host and viral DNA synthesis in the undifferentiated cells.
引用
收藏
页码:209 / 216
页数:8
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