Momoeda M, Kawase M, Jane S M, Miyamura K, Young N S, Kajigaya S
Hematology Branch, National Heart, Lung, and Blood Institute, Bethesda, Maryland 20892.
J Virol. 1994 Nov;68(11):7159-68. doi: 10.1128/JVI.68.11.7159-7168.1994.
We performed a systematic study to identify cellular factors that bound to the terminal repeat region of B19 parvovirus. Using electrophoretic mobility shift assays, we detected one cellular factor which prominently bound to the repeat region. The factor was purified from K562 nuclear extract by specific DNA affinity column chromatography and identified as YY1, a multifunctional transcription factor. Of multiple possible YY1 binding sites in the upstream region of the P6 promoter, three showed specific strong binding. Transcription enhancement by YY1 was demonstrated in vitro by transient transfection assays. In studies using truncated and mutated versions of this region, YY1 activity was diminished by the alteration of any two of these three sites and abolished by the alteration of all three sites. Our results suggest that YY1 is a positive regulator of B19 parvovirus transcription.
我们进行了一项系统性研究,以鉴定与B19细小病毒末端重复区域结合的细胞因子。利用电泳迁移率变动分析,我们检测到一种与重复区域显著结合的细胞因子。该因子通过特异性DNA亲和柱层析从K562细胞核提取物中纯化出来,并被鉴定为YY1,一种多功能转录因子。在P6启动子上游区域的多个可能的YY1结合位点中,有三个显示出特异性强结合。通过瞬时转染分析在体外证明了YY1对转录的增强作用。在使用该区域的截短和突变版本的研究中,这三个位点中任意两个位点的改变都会使YY1活性降低,而所有三个位点的改变则会使其活性完全丧失。我们的结果表明,YY1是B19细小病毒转录的正调节因子。