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BALB/c小鼠内源性亲嗜性前病毒的分子与生物学特征

Molecular and biological characterization of the endogenous ecotropic provirus of BALB/c mice.

作者信息

Horowitz J M, Risser R

出版信息

J Virol. 1985 Dec;56(3):798-806. doi: 10.1128/JVI.56.3.798-806.1985.

Abstract

We have isolated two identical molecular clones of the single, endogenous ecotropic provirus of BALB/c mice. The BALB/c clones are approximately 1/10 as infectious as an exogenous proviral clone derived from AKR mice, p623. Transfection of mouse cells with each BALB/c proviral clone yielded XC-negative, N-tropic, ecotropic virus. Cotransfection of subgenomic fragments of p623 and the BALB/c provirus did not increase infectivity to the level observed for p623; however, a 292-base-pair fragment of the p623 env gene was found to rescue XC-plaque formation. Sequence analysis showed that the XC-negative BALB/c provirus differed from the XC-positive AKR-derived provirus at a single nucleotide at the junction of the gp70 and p15E envelope proteins. Extensive sequence analysis of the BALB/c endogenous provirus showed that it differed from the sequence of the AKR-derived provirus at approximately 0.5% of 4,500 sequenced nucleotides. In addition, the BALB/c long terminal repeat contains a single copy of the enhancer-containing sequences that are repeated twice in p623. The limited variation between the ecotropic proviruses of BALB/c mice and AKR mice suggests that few cycles of reverse transcription separate these viral genomes.

摘要

我们分离出了BALB/c小鼠单一内源性亲嗜性前病毒的两个相同分子克隆。BALB/c克隆的感染性约为源自AKR小鼠的外源性前病毒克隆p623的1/10。用每个BALB/c前病毒克隆转染小鼠细胞,产生了XC阴性、N嗜性、亲嗜性病毒。p623亚基因组片段与BALB/c前病毒的共转染并未使感染性增加到p623所观察到的水平;然而,发现p623 env基因的一个292个碱基对的片段可挽救XC噬斑形成。序列分析表明,XC阴性的BALB/c前病毒在gp70和p15E包膜蛋白交界处的单个核苷酸处与XC阳性的源自AKR的前病毒不同。对BALB/c内源性前病毒的广泛序列分析表明,在4500个测序核苷酸中,它与源自AKR的前病毒序列的差异约为0.5%。此外,BALB/c长末端重复序列包含含增强子序列的单拷贝,这些序列在p623中重复两次。BALB/c小鼠和亲嗜性前病毒与AKR小鼠亲嗜性前病毒之间有限的差异表明,这些病毒基因组之间很少有逆转录循环。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93c6/252650/1665b8a3eef3/jvirol00117-0156-a.jpg

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