Selective inhibition of nuclear steroid receptor function by a protein from a human tumorigenic poxvirus

被引:15
作者
Chen, N
Baudino, T
MacDonald, PN
Green, M
Kelley, WL
Burnett, JW
Buller, RML [1 ]
机构
[1] St Louis Univ, Ctr Hlth Sci, Dept Mol Microbiol & Immunol, St Louis, MO 63104 USA
[2] St Louis Univ, Ctr Hlth Sci, Dept Pharmacol & Physiol Sci, St Louis, MO 63104 USA
[3] Ctr Med Univ Geneva, Dept Biochim Med, CH-1211 Geneva, Switzerland
[4] Univ Maryland, Sch Med, Dept Dermatol, Baltimore, MD 21201 USA
关键词
D O I
10.1006/viro.2000.0410
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The poxvirus molluscum contagiosum (MC) has a worldwide distribution and its prevalence is on the rise. Here we report that the MCV MC013L protein inhibits glucocorticoid and vitamin D, but not retinoid or estrogen, nuclear receptor transactivation. A direct interaction of MC013L with glucocorticoid and vitamin D receptor is supported by yeast two-hybrid, GST pull-down, and far Western blot analyses. Glucocorticoids act as potent inhibitors of keratinocyte proliferation, while vitamin D and retinoids promote and block terminal differentiation, respectively. Therefore, MC013L may promote efficient virus replication by blocking the differentiation of infected keratinocytes. MC013L may be the first member of a new class of poxvirus proteins that directly modulate nuclear receptor-mediated transcription, (C) 2000 Academic Press.
引用
收藏
页码:17 / 25
页数:9
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