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病毒E1和E2蛋白诱导牛乳头瘤病毒1型复制起点的结构变化。

Induction of structural changes in the bovine papillomavirus type 1 origin of replication by the viral E1 and E2 proteins.

作者信息

Gillette T G, Lusky M, Borowiec J A

机构信息

Department of Biochemistry, New York University Medical Center, NY 10016.

出版信息

Proc Natl Acad Sci U S A. 1994 Sep 13;91(19):8846-50. doi: 10.1073/pnas.91.19.8846.

Abstract

Chemical and enzymatic probing techniques were used to examine the interaction of the bovine papillomavirus type 1 E1 and E2 proteins with the viral origin of replication (ori). E1 was found to generate significant distortions to the structure of ori, as assayed by KMnO4 oxidation of DNA. The primary site of ori distortion was located within and adjacent to the AT-element of the core replicator sequence, although a number of minor structural transitions were also detected. The induction of these structural changes required ATP and appeared to require ATP hydrolysis. E2 was found to decrease the amount of E1 required for ori distortion but did not significantly alter the pattern of structural distortion. In contrast, the presence of E2 resulted in a biphasic mechanism for E1 binding to ori, as assayed by nuclease protection. Under these conditions, E1 bound preferentially to the dyad symmetry region containing the conserved Hpa I site. Higher levels of E1 were required for binding to the adjacent ori AT-rich region. Thus, these data suggest that E2 can order the stepwise binding of E1 to ori.

摘要

运用化学和酶促探测技术来检测牛乳头瘤病毒1型E1和E2蛋白与病毒复制起点(ori)之间的相互作用。通过DNA的高锰酸钾氧化检测发现,E1会对ori的结构产生显著扭曲。ori扭曲的主要位点位于核心复制子序列的AT元件内部及附近,不过也检测到了一些较小的结构转变。这些结构变化的诱导需要ATP,且似乎需要ATP水解。研究发现,E2可减少ori扭曲所需的E1量,但并未显著改变结构扭曲模式。相比之下,通过核酸酶保护检测发现,E2的存在导致E1与ori结合呈现双相机制。在这些条件下,E1优先结合至含有保守Hpa I位点的二元对称区域。结合相邻的富含AT的ori区域则需要更高水平的E1。因此,这些数据表明E2能够调控E1与ori的逐步结合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27ce/44703/32ecc77e7867/pnas01141-0128-a.jpg

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