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鼠类艾滋病诱导序列的可能起源。

Possible origin of murine AIDS-inducing sequence.

作者信息

Kubo Y, Higo K, Kobayashi H, Ono T, Iwama Y, Yanagawa S, Adachi A, Ishimoto A

机构信息

Department of Viral Oncology, Kyoto University, Japan.

出版信息

Leukemia. 1997 Apr;11 Suppl 3:163-6.

PMID:9209331
Abstract

The murine AIDS (MAIDS) virus has a unique sequence in its gag p12 region. A transcript which hybridizes with this sequence is expressed in normal C57BL/6 mice. This transcript has been proposed to be the origin of the MAIDS virus, since the virus was originally isolated from radiation-induced leukemic C57BL/6 mice. The transcript, designated Edv, was molecularly cloned and sequenced. Compared with the nucleotide sequence of the helper LP-BM5 ecotropic virus, the pathogenic defective MAIDS virus has 16-bp deletions and a 1-bp insertion in the 5' and 3' regions of the gag p12 sequence, respectively, and the Edv transcript contains only a 3-bp deletion. Therefore, the amino acid sequence of the gag p12 region of the MAIDS virus is less homologous to that of the helper virus and Edv transcript due to the frameshift mutations. This suggested that the MAIDS virus was generated by such frameshift mutations in the gag p12 region during recombination between the helper virus and the Edv or a related sequence.

摘要

鼠艾滋病(MAIDS)病毒在其gag p12区域有独特序列。一种与该序列杂交的转录本在正常C57BL/6小鼠中表达。由于该病毒最初是从辐射诱导的白血病C57BL/6小鼠中分离出来的,因此该转录本被认为是MAIDS病毒的起源。将该转录本命名为Edv,进行了分子克隆和测序。与辅助性LP - BM5嗜亲性病毒的核苷酸序列相比,致病性缺陷MAIDS病毒在gag p12序列的5'和3'区域分别有16个碱基对的缺失和1个碱基对的插入,而Edv转录本仅包含3个碱基对的缺失。因此,由于移码突变,MAIDS病毒gag p12区域的氨基酸序列与辅助病毒和Edv转录本的氨基酸序列同源性较低。这表明MAIDS病毒是在辅助病毒与Edv或相关序列重组过程中,gag p12区域发生此类移码突变而产生的。

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