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BK病毒增强子元件和一种人类细胞同源物。

BK viral enhancer element and a human cellular homolog.

作者信息

Rosenthal N, Kress M, Gruss P, Khoury G

出版信息

Science. 1983 Nov 18;222(4625):749-55. doi: 10.1126/science.6314501.

Abstract

Comparison of two closely related primate papovaviruses, simian virus 40 (SV40) and human BK virus (BKV), reveals that the only region of extensive divergence, the tandem sequences adjacent to the origins of DNA replication, is responsible in SV40 for enhancing early gene expression. This study demonstrates a similar enhancer function for the analogous repeated region in BKV. The dissimilarity in sequence of the BKV and SV40 enhancer elements suggests that they may have been acquired since SV40 and BKV diverged. A locus cloned from the human genome homologous to the BKV tandem repeats has been shown to function as low level enhancer element in mammalian cells. These data support the hypothesis that viral enhancer sequences may be evolutionarily related to host cell sequences.

摘要

对两种密切相关的灵长类乳头瘤病毒——猴病毒40(SV40)和人BK病毒(BKV)进行比较后发现,唯一存在广泛差异的区域,即与DNA复制起点相邻的串联序列,在SV40中负责增强早期基因表达。本研究证明BKV中类似的重复区域也具有类似的增强子功能。BKV和SV40增强子元件序列的差异表明,它们可能是在SV40和BKV分化后获得的。从人类基因组中克隆的一个与BKV串联重复序列同源的位点已被证明在哺乳动物细胞中作为低水平增强子元件发挥作用。这些数据支持了病毒增强子序列可能在进化上与宿主细胞序列相关的假说。

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