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1型牛乳头瘤病毒DNA的复制效率取决于与复制起点不同的顺式作用序列。

Replication efficiency of bovine papillomavirus type 1 DNA depends on cis-acting sequences distinct from the replication origin.

作者信息

Pierrefite V, Cuzin F

机构信息

INSERM U273, Université de Nice, France.

出版信息

J Virol. 1995 Dec;69(12):7682-7. doi: 10.1128/JVI.69.12.7682-7687.1995.

Abstract

The viral elements required for the initiation of replication of bovine papillomavirus type 1 DNA include the origin region and two trans-acting factors, the E1 and E2 proteins. We now report that the replication efficiency of a DNA molecule which contains these three elements is modulated by other viral sequences. By measuring the extent of replication of deleted viral genomes in transfected mouse cells, we identified sequences required for maximal efficiency. Addition of these sequences to a construct carrying only the minimal origin region increased its replication. Among these cis-active elements, we identified a 69-bp fragment (nucleotides 4921 to 4990) which contains at least two binding sites for cellular proteins. One of them is the murine protein termed CDEBP, which recognizes the octameric motif ATCACGTG, identical to the yeast CDEI element. Either deletions affecting this CDEI box or a point mutation which impairs binding of CDEBP markedly decreased the extent of viral DNA replication. They had no detectable effect on viral transcription.

摘要

1型牛乳头瘤病毒DNA复制起始所需的病毒元件包括起始区域和两个反式作用因子,即E1和E2蛋白。我们现在报告,包含这三种元件的DNA分子的复制效率受其他病毒序列的调节。通过测量转染的小鼠细胞中缺失病毒基因组的复制程度,我们确定了实现最大效率所需的序列。将这些序列添加到仅携带最小起始区域的构建体中可增加其复制。在这些顺式活性元件中,我们鉴定出一个69碱基对的片段(核苷酸4921至4990),其包含至少两个细胞蛋白结合位点。其中之一是称为CDEBP的鼠蛋白,它识别八聚体基序ATCACGTG,与酵母CDEI元件相同。影响该CDEI框的缺失或损害CDEBP结合的点突变均显著降低病毒DNA复制程度。它们对病毒转录没有可检测到的影响。

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