Feedback regulation between orphan nuclear receptor TR2 and human papilloma virus type 16

被引:6
|
作者
Collins, LL
Lin, DL
Mu, XM
Chang, CS [1 ]
机构
[1] Univ Rochester, Med Ctr, George Whipple Lab Canc Res, Rochester, NY 14642 USA
[2] Univ Rochester, Med Ctr, Dept Pathol, Rochester, NY 14642 USA
[3] Univ Rochester, Med Ctr, Dept Urol, Rochester, NY 14642 USA
[4] Univ Rochester, Med Ctr, Dept Radiat Oncol, Rochester, NY 14642 USA
[5] Univ Rochester, Med Ctr, Ctr Canc, Rochester, NY 14642 USA
关键词
D O I
10.1074/jbc.M104145200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The human TR2 orphan receptor (TR2), initially isolated from testis and prostate cDNA libraries, is a member of the steroid receptor superfamily. TR2 can regulate several target genes via binding to a consensus response element (AGGTCA) in direct repeat orientation (AGGTCAX((n))AGGTCA, n = 0-6). Here show that TR2 is able to induce the expression of human papilloma virus type 16 (HPV-16) genes via binding to a DR4 response element in the long control region of HPV-16. Additionally, one of the HPV-16 gene products, the E6 oncogene, regulates TR2 gene expression. A likely mechanism for this regulation involves E6-mediate-degradation of the tumor suppressor p53, a protein known to suppress TR2 expression. Together our data provide evidence for feedback regulation between TR2 and HPV-16, which represents a novel regulatory pathway involving a member of the steroid receptor superfamily and the HPV-16 DNA tumor virus.
引用
收藏
页码:27316 / 27321
页数:6
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