The human papillomavirus18 E7 protein inhibits CENP-C binding to α-satellite DNA

被引:5
作者
Yaginuma, Yuji [1 ]
Yoshimoto, Masafumi [1 ]
Eguchi, Ayami [1 ]
Tokuda, Aoi [2 ]
Takahashi, Shoko [2 ]
机构
[1] Kumamoto Univ, Fac Life Sci, Dept Oncol, Grad Sch Hlth Sci,Chou Ku, Kumamoto 8620976, Japan
[2] Kumamoto Univ, Fac Life Sci, Sch Hlth Sci, Chuou Ku, Kumamoto 8620976, Japan
关键词
HPV; E7; CENP-C; alpha-Satellite DNA; MITOTIC CHECKPOINT; PCR AMPLIFICATION; CANCER; ANEUPLOIDY; RISK; INACTIVATION; ONCOPROTEINS; CAPACITY; SEQUENCE;
D O I
10.1016/j.virusres.2015.04.019
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Human papillomavirus (HPV) infection leads to aneuploidy, a numerical chromosomal aberration that is caused by dysregulation of chromosomal segregation. We previously found that the E7 proteins of high-risk HPVs, but not of low-risk HPVs, could bind to centromere protein-C (CENP-C). In this study, we first found that CENP-C could bind centromere alpha-satellite DNAs using ChIP analysis and HA-tagged CENP-C/nuc transfected 293T cells. We then investigated if HA-CENP-C/nuc binding to alpha-satellite DNAs was affected by the E7 proteins of high- or low-risk HPVs. We found that transfection of the FLAG tagged HPV18 E7 inhibited the binding of HA-CENP-C/nuc to alpha-satellite DNAs. This finding was confirmed in HeLa S3 cells transfected with siRNA targeted to HPV18 E7 expression. We therefore speculate that altered function of kinetochores as a result of inhibition of CENP-C and alpha-satellite DNAs binding may be associated with the chromosomal abnormalities observed in HPV18-positive cancers. (C) 2015 Elsevier B.V. All rights reserved.
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页码:27 / 32
页数:6
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