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特定转录因子刺激猿猴病毒40和多瘤病毒的DNA复制起点。

Specific transcription factors stimulate simian virus 40 and polyomavirus origins of DNA replication.

作者信息

Guo Z S, DePamphilis M L

机构信息

Department of Cell and Developmental Biology, Roche Research Center, Nutley, New Jersey 07110.

出版信息

Mol Cell Biol. 1992 Jun;12(6):2514-24. doi: 10.1128/mcb.12.6.2514-2524.1992.

Abstract

The origins of DNA replication (ori) in simian virus 40 (SV40) and polyomavirus (Py) contain an auxiliary component (aux-2) composed of multiple transcription factor binding sites. To determine whether this component stimulated replication by binding specific transcription factors, aux-2 was replaced by synthetic oligonucleotides that bound a single transcription factor. Sp1 and T-antigen (T-ag) sites, which exist in the natural SV40 aux-2 sequence, provided approximately 75 and approximately 20%, respectively, of aux-2 activity when transfected into monkey cells. In cell extracts, only T-ag sites were active. AP1 binding sites could replace completely either SV40 or Py aux-2. Mutations that eliminated AP1 binding also eliminated AP1 stimulation of replication. Yeast GAL4 binding sites that strongly stimulated transcription in the presence of GAL4 proteins failed to stimulate SV40 DNA replication, although they did partially replace Py aux-2. Stimulation required the presence of proteins consisting of the GAL4 DNA binding domain fused to specific activation domains such as VP16 or c-Jun. These data demonstrate a clear role for transcription factors with specific activation domains in activating both SV40 and Py ori. However, no correlation was observed between the ability of specific proteins to stimulate promoter activity and their ability to stimulate origin activity. We propose that only transcription factors whose specific activation domains can interact with the T-ag initiation complex can stimulate SV40 and Py ori-core activity.

摘要

猴病毒40(SV40)和多瘤病毒(Py)的DNA复制起始点(ori)含有一个由多个转录因子结合位点组成的辅助成分(aux-2)。为了确定该成分是否通过结合特定转录因子来刺激复制,aux-2被能结合单个转录因子的合成寡核苷酸所取代。天然SV40的aux-2序列中存在的Sp1和T抗原(T-ag)位点,转染到猴细胞中时分别提供了约75%和约20%的aux-2活性。在细胞提取物中,只有T-ag位点具有活性。AP1结合位点可以完全替代SV40或Py的aux-2。消除AP1结合的突变也消除了AP1对复制的刺激。在存在GAL4蛋白的情况下强烈刺激转录的酵母GAL4结合位点未能刺激SV40 DNA复制,尽管它们确实部分替代了Py的aux-2。刺激需要存在由与特定激活域(如VP16或c-Jun)融合的GAL4 DNA结合域组成的蛋白质。这些数据证明了具有特定激活域的转录因子在激活SV40和Py ori方面的明确作用。然而,未观察到特定蛋白质刺激启动子活性的能力与其刺激起始点活性的能力之间存在相关性。我们提出,只有其特定激活域能够与T-ag起始复合物相互作用的转录因子才能刺激SV40和Py ori核心活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a695/364444/78303c616f9d/molcellb00028-0073-a.jpg

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