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在嗜肝DNA病毒正链DNA合成过程中,负链DNA模板上末端冗余序列的序列同一性对于模板转换是必要的,但并不充分。

Sequence identity of the terminal redundancies on the minus-strand DNA template is necessary but not sufficient for the template switch during hepadnavirus plus-strand DNA synthesis.

作者信息

Loeb D D, Gulya K J, Tian R

机构信息

McArdle Laboratory for Cancer Research, University of Wisconsin Medical School, Madison 53706, USA.

出版信息

J Virol. 1997 Jan;71(1):152-60. doi: 10.1128/JVI.71.1.152-160.1997.

Abstract

The template for hepadnavirus plus-strand DNA synthesis is a terminally redundant minus-strand DNA. An intramolecular template switch during plus-strand DNA synthesis, which permits plus-strand DNA elongation, has been proposed to be facilitated by this terminal redundancy, which is 7 to 9 nucleotides long. The aim of this study was to determine whether the presence of identical copies of the redundancy on the minus-strand DNA template was necessary and/or sufficient for the template switch and at what position(s) within the redundancy the switch occurs for duck hepatitis B virus. When dinucleotide insertions were placed within the copy of the redundancy at the 3' end of the minus-strand DNA template, novel sequences were copied into plus-strand DNA. The generation of these novel sequences could be explained by complete copying of the redundancy at the 5' end of the minus-strand DNA template followed by a template switch and then extension from a mismatched 3' terminus. In a second set of experiments, it was found that when one copy of the redundancy had either three or five nucleotides replaced the template switch was inhibited. When the identical, albeit mutant, sequences were restored in both copies of the redundancy, template switching was not necessarily restored. Our results indicate that the terminal redundancy on the minus-strand DNA template is necessary but not sufficient for template switching.

摘要

嗜肝DNA病毒正链DNA合成的模板是末端冗余的负链DNA。有人提出,正链DNA合成过程中的分子内模板转换促进了正链DNA的延伸,而这种模板转换是由长度为7至9个核苷酸的末端冗余所推动的。本研究的目的是确定负链DNA模板上冗余的相同拷贝的存在对于模板转换是否必要和/或充分,以及对于鸭乙型肝炎病毒而言,模板转换发生在冗余内的哪个位置。当在负链DNA模板3'端的冗余拷贝内插入二核苷酸时,新序列被复制到正链DNA中。这些新序列的产生可以通过负链DNA模板5'端冗余的完全复制、随后的模板转换以及从不匹配的3'末端延伸来解释。在第二组实验中,发现当冗余的一个拷贝中有三个或五个核苷酸被替换时,模板转换受到抑制。当冗余的两个拷贝中恢复相同的(尽管是突变的)序列时,模板转换不一定恢复。我们的结果表明,负链DNA模板上的末端冗余对于模板转换是必要的,但不是充分的。

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