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弗瑞德白血病病毒的Fv-1宿主限制:宿主范围变体的寡核苷酸分析

Fv-1 host restriction of Friend leukemia virus: oligonucleotide analysis of host range variants.

作者信息

Duttagupta S, Soeiro R

出版信息

J Virol. 1981 Apr;38(1):376-9. doi: 10.1128/JVI.38.1.376-379.1981.

Abstract

The Fv-1 murine gene controls predominantly the replication of leukemia viruses of murine cells. Forced passage by B-tropic Friend leukemia virus in the restrictive host cells (NIH, Fv-1n/n) results in viral progeny capable of replicating efficiently in murine cells of any Fv-1 type, which are denoted as NB-tropic virus. We have studied the RNase T1-resistant oligonucleotide pattern of a series of NB-tropic Friend virus isolates and have been able to show changes from the parental B-tropic virus which occur at the 5' end of the genome. Cloned NB-tropic virus falls into three classes, demonstrating either four, one, or no apparent changes in the genome. These results suggest the possibility that conversion to NB tropism occurs by a recombination mechanism but, since change to NB tropism can occur without any observable oligonucleotide alteration, they do not confirm that any single oligonucleotide is diagnostic of NB tropism.

摘要

Fv-1小鼠基因主要控制鼠细胞中白血病病毒的复制。在限制性宿主细胞(NIH,Fv-1n/n)中,由B嗜性弗氏白血病病毒强制传代产生的病毒后代能够在任何Fv-1类型的鼠细胞中高效复制,这些病毒后代被称为NB嗜性病毒。我们研究了一系列NB嗜性弗氏病毒分离株的核糖核酸酶T1抗性寡核苷酸图谱,并能够显示出与亲代B嗜性病毒相比,在基因组5'端发生的变化。克隆的NB嗜性病毒分为三类,基因组中分别显示出四种、一种或无明显变化。这些结果表明,转换为NB嗜性可能是通过重组机制发生的,但是,由于转换为NB嗜性可以在没有任何可观察到的寡核苷酸改变的情况下发生,因此它们不能证实任何单个寡核苷酸可作为NB嗜性的诊断依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e41b/171161/09baa4a7420e/jvirol00004-0385-a.jpg

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