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

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Abstract

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 MCO13L 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. © 2000 Academic Press.

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Chen, N., Baudino, T., MacDonald, P. N., Green, M., Kelley, W. L., Burnett, J. W., & Buller, R. M. L. (2000). Selective inhibition of nuclear steroid receptor function by a protein from a human tumorigenic poxvirus. Virology, 274(1), 17–25. https://doi.org/10.1006/viro.2000.0410

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