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劳氏肉瘤病毒转化的非产生型和产生型动物细胞中的传染性病毒DNA。

Infectious viral DNA in Rous sarcoma virus-transformed nonproducer and producer animal cells.

作者信息

Hill M, Hillova J, Dantchev D, Mariage R, Goubin G

出版信息

Cold Spring Harb Symp Quant Biol. 1975;39 Pt 2:1015-25. doi: 10.1101/sqb.1974.039.01.117.

Abstract

Nonproducer and producer RSV-transformed cells and producer nontransforming virus-infected cells harbor viral DNA specifying the respective avian tumor virus. In nonproducer Rous sarcoma cells, the residing viral DNA is linear, double-stranded and covalently linked to the chromosomal DNA. Both double-stranded and single-stranded forms of RSV DNA transfect chicken cells. The progeny virus is indistinguishable from the DNA parent with respect to the morphological, biological and antigenic properties. Unlike the DNA extracted from nonproducer RSV-transformed mammalian cells, that extracted from producer RSV-transformed chicken cells gives rise, in transfection experiments, to both sarcoma virus and its nontransforming derivative. The DNA from nontransforming virus-infected chicken cells generates only nontransforming viruses. The frequency of nontransforming virus recovery is different from that of sarcoma virus recovery, the latter being a nonlinear function of the amount of transfecting DNA, while the former may suggest a linear relationship. On the other hand, the end-point dilution of transfecting DNA for sarcoma virus recovery is approximately the same as that for nontransforming virus recovery. The following is assumed: Sarcoma viruses and nontransforming derivatives are recovered from two different species of viral DNA which carry or lack, respectively, the transforming genetic material. The size of double-stranded viral DNA is substantially smaller than 20 times 10(6) daltons. In transfection experiments, the sarcoma virus DNA is first integrated into the host cell genome before being expressed, while the nontransforming viral DNA apparently bypasses the integration step. The latter DNA generates the progeny virus when taken up, carried, and transcribed in a permissive cell.

摘要

非产生型和产生型呼吸道合胞病毒(RSV)转化细胞以及产生型非转化病毒感染细胞都含有指定相应禽肿瘤病毒的病毒DNA。在非产生型劳氏肉瘤细胞中,存在的病毒DNA是线性双链的,并且与染色体DNA共价连接。RSV DNA的双链和单链形式都能转染鸡细胞。子代病毒在形态、生物学和抗原特性方面与DNA亲本无法区分。与从非产生型RSV转化的哺乳动物细胞中提取的DNA不同,从产生型RSV转化的鸡细胞中提取的DNA在转染实验中会产生肉瘤病毒及其非转化衍生物。来自非转化病毒感染鸡细胞的DNA仅产生非转化病毒。非转化病毒回收的频率与肉瘤病毒回收的频率不同,后者是转染DNA量的非线性函数,而前者可能表明存在线性关系。另一方面,用于肉瘤病毒回收的转染DNA的终点稀释与用于非转化病毒回收的终点稀释大致相同。假设如下:肉瘤病毒和非转化衍生物是从两种不同的病毒DNA中回收的,它们分别携带或缺乏转化遗传物质。双链病毒DNA的大小明显小于20×10⁶道尔顿。在转染实验中,肉瘤病毒DNA在表达之前首先整合到宿主细胞基因组中,而非转化病毒DNA显然绕过了整合步骤。后一种DNA在被允许的细胞中被摄取、携带和转录时会产生子代病毒。

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