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[肿瘤病毒基因组的DNA形式]

[DNA form of the genome of oncornaviruses].

作者信息

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

出版信息

Bull Cancer. 1975 Apr-Jun;62(2):183-94.

PMID:175870
Abstract

The oncornaviruses share several biological, biochemical, and structural properties that distinguish them from other RNA viruses. Rous sarcoma virus, a representative of avian oncornaviruses, manifests two major functions: cell transformation and virus replication. Both functions are independent, and are expressed separately in defective viruses. The virus has a 60-70S RNA, composed of 35 S subunits. It appears that each subunit of viral RNA carries the same genetic information and, furthermore, that 10% of this information is coding for cell transformation. Without this 10% the virus can still replicate. The RNA genome is expressed when the virus penetrates a sensitive cell, provided the virus carries an active reverse transcriptase. Virus-transformed cells possess a DNA form of the viral genome. The viral DNA is infectious, and can lead, upon transfection of permissive cells, to the production of a new viral progeny. We have established that the minimum molecular weight of the viral DNA is 6 X 10(6) daltons, and that this DNA is covalently bound to the chromosomal DNA. Also by examining the frequency of transfection events in the DNA-treated cells we suggest that transfection is a single-hit phenomenon. It follows that viral DNA of 6 X 10(6) daltons carries all the genetic information to code for the virus production. It seems likely that the transfection mechanism giving rise to transforming viruses is different from that producing nontransforming segments. In general terms, the experimental data indicate that certain RNAs and DNAs could accomplish malignant transformation if they are able to penetrate into the cell and give rise to the DNA forms which could be integrated into the cellular genome.

摘要

肿瘤病毒具有一些生物学、生物化学和结构特性,这些特性将它们与其他RNA病毒区分开来。劳氏肉瘤病毒是禽肿瘤病毒的代表,具有两种主要功能:细胞转化和病毒复制。这两种功能相互独立,在缺陷病毒中分别表达。该病毒有一个60 - 70S的RNA,由35S亚基组成。似乎病毒RNA的每个亚基都携带相同的遗传信息,而且,这些信息的10%编码细胞转化。没有这10%,病毒仍能复制。当病毒携带活性逆转录酶并穿透敏感细胞时,RNA基因组得以表达。病毒转化的细胞拥有病毒基因组的DNA形式。病毒DNA具有感染性,转染允许细胞后可导致产生新的病毒后代。我们已经确定病毒DNA的最小分子量为6×10⁶道尔顿,并且这种DNA与染色体DNA共价结合。通过检测DNA处理细胞中转染事件的频率,我们还表明转染是一种单打击现象。由此可见,6×10⁶道尔顿的病毒DNA携带了编码病毒产生的所有遗传信息。引发转化病毒的转染机制似乎与产生非转化片段的机制不同。一般来说,实验数据表明某些RNA和DNA如果能够穿透细胞并产生可整合到细胞基因组中的DNA形式,就可以完成恶性转化。

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