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嗜异性前病毒包膜序列在小家鼠种系中不存在。

Amphotropic proviral envelope sequences are absent from the Mus germ line.

作者信息

O'Neill R R, Hartley J W, Repaske R, Kozak C A

出版信息

J Virol. 1987 Jul;61(7):2225-31. doi: 10.1128/JVI.61.7.2225-2231.1987.

Abstract

We derived an amphotropic murine leukemia virus (MuLV) type-specific probe for use in Southern blot hybridizations with cloned and genomic DNAs. A 133-base-pair RsaI-RsaI fragment from the 5' env region of the amphotropic viral isolate 4070A was subcloned into M13mp18 and radiolabeled in vitro. The probe detected the proviral DNAs in mink cells infected with seven different amphotropic MuLV isolates. The probe did not cross hybridize with the DNAs of molecular clones of ecotropic, mink cell focus-forming, or xenotropic MuLVs; nor did it anneal to the proviral DNAs of four xenotropic or six mink cell focus-forming viral isolates grown in mink cells. DNAs of 12 inbred laboratory mouse strains and more than 15 different wild mouse species and subspecies were examined for the presence of endogenous amphotropic env-related fragments. Amphotropic env-related sequences were found only in the DNAs of wild mice trapped in southern California in an area previously shown to harbor mice producing infectious amphotropic virus. Restriction enzyme analyses of DNAs from these mice showed that amphotropic sequences were not present as germ line copies but were the result of congenital or horizontal infection or both in this population. The DNAs of 11 various mammalian and avian species, including both natural predators of mice and squabs from the farms with virus-positive mice, lacked amphotropic envelope-related sequences.

摘要

我们制备了一种嗜异性鼠白血病病毒(MuLV)型特异性探针,用于与克隆DNA和基因组DNA进行Southern印迹杂交。从嗜异性病毒分离株4070A的5'env区域获得的一个133碱基对的RsaI-RsaI片段被亚克隆到M13mp18中,并在体外进行放射性标记。该探针可检测感染七种不同嗜异性MuLV分离株的水貂细胞中的前病毒DNA。该探针不会与亲嗜性、水貂细胞集落形成性或异嗜性MuLV分子克隆的DNA发生交叉杂交;也不会与在水貂细胞中生长的四种异嗜性或六种水貂细胞集落形成性病毒分离株的前病毒DNA退火。检测了12种近交系实验小鼠品系以及15种以上不同野生小鼠物种和亚种的DNA中是否存在内源性嗜异性env相关片段。仅在加利福尼亚州南部捕获的野生小鼠的DNA中发现了嗜异性env相关序列,该区域先前已显示存在产生传染性嗜异性病毒的小鼠。对这些小鼠的DNA进行限制性酶切分析表明,嗜异性序列并非以种系拷贝的形式存在,而是该种群中先天性感染或水平感染或两者兼有的结果。11种不同的哺乳动物和鸟类物种的DNA,包括小鼠的天然捕食者以及来自有病毒阳性小鼠的农场的雏鸽,均缺乏嗜异性包膜相关序列。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f5d/283686/f9a16bd6c3ff/jvirol00098-0175-a.jpg

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