Selective inhibition of nuclear steroid receptor function by a protein from a human tumorigenic poxvirus
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Chen, N
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机构:St Louis Univ, Ctr Hlth Sci, Dept Mol Microbiol & Immunol, St Louis, MO 63104 USA
Chen, N
Baudino, T
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机构:St Louis Univ, Ctr Hlth Sci, Dept Mol Microbiol & Immunol, St Louis, MO 63104 USA
Baudino, T
MacDonald, PN
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机构:St Louis Univ, Ctr Hlth Sci, Dept Mol Microbiol & Immunol, St Louis, MO 63104 USA
MacDonald, PN
Green, M
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机构:St Louis Univ, Ctr Hlth Sci, Dept Mol Microbiol & Immunol, St Louis, MO 63104 USA
Green, M
Kelley, WL
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机构:St Louis Univ, Ctr Hlth Sci, Dept Mol Microbiol & Immunol, St Louis, MO 63104 USA
Kelley, WL
Burnett, JW
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机构:St Louis Univ, Ctr Hlth Sci, Dept Mol Microbiol & Immunol, St Louis, MO 63104 USA
Burnett, JW
Buller, RML
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St Louis Univ, Ctr Hlth Sci, Dept Mol Microbiol & Immunol, St Louis, MO 63104 USASt Louis Univ, Ctr Hlth Sci, Dept Mol Microbiol & Immunol, St Louis, MO 63104 USA
Buller, RML
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[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
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.