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由多聚嘌呤序列的中央拷贝所界定的人类免疫缺陷病毒未整合线性DNA中的单链缺口。

A single-stranded gap in human immunodeficiency virus unintegrated linear DNA defined by a central copy of the polypurine tract.

作者信息

Charneau P, Clavel F

机构信息

Unité d'Oncologie Virale, Département SIDA et Rétrovirus, Institut Pasteur, Paris, France.

出版信息

J Virol. 1991 May;65(5):2415-21. doi: 10.1128/JVI.65.5.2415-2421.1991.

Abstract

The structure of unintegrated human immunodeficiency virus type 1 (HIV-1) DNA from acutely infected human lymphoid cells was analyzed by nuclease S1 cleavage. We observed a unique, discrete single-stranded gap in unintegrated linear DNA molecules, located near the center of the genome. Oligonucleotide primer extension experiments determined that the downstream limit of this gap coincides with the last nucleotide of a central copy of the polypurine tract found in all sequenced lentivirus genomes. Other retroviruses have only one copy of the polypurine tract at the 5' boundary of the 3' long terminal repeat, which has been shown to determine initiation of retroviral DNA plus-strand synthesis. We conclude from our observations that the central repeat of the polypurine tract can create an additional site for plus-strand synthesis initiation in lentiviruses. The central single-stranded gap was not found in circular DNA molecules, the vast majority of them carrying only one long terminal repeat. This finding suggests that the generation of such circular molecules is associated with early DNA ligation events.

摘要

通过核酸酶S1切割分析了急性感染的人淋巴细胞中未整合的1型人类免疫缺陷病毒(HIV-1)DNA的结构。我们在未整合的线性DNA分子中观察到一个独特的、离散的单链缺口,位于基因组中心附近。寡核苷酸引物延伸实验确定,这个缺口的下游边界与所有已测序慢病毒基因组中发现的多聚嘌呤序列中央拷贝的最后一个核苷酸一致。其他逆转录病毒在3'长末端重复序列的5'边界只有一个多聚嘌呤序列拷贝,该序列已被证明可决定逆转录病毒DNA正链合成的起始。我们从观察结果得出结论,多聚嘌呤序列的中央重复序列可在慢病毒中为正链合成起始创造一个额外位点。在环状DNA分子中未发现中央单链缺口,其中绝大多数只携带一个长末端重复序列。这一发现表明,此类环状分子的产生与早期DNA连接事件有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/920c/240594/f5229d66d8b4/jvirol00048-0275-a.jpg

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