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5型腺病毒与12型腺病毒重组体转化细胞的致瘤能力对早期区域1表达的依赖性

Dependence of tumor-forming capacities of cells transformed by recombinants between adenovirus types 5 and 12 on expression of early region 1.

作者信息

Shiroki K, Maruyama K, Saito I, Fukui Y, Yazaki K, Shimojo H

出版信息

J Virol. 1982 May;42(2):708-18. doi: 10.1128/JVI.42.2.708-718.1982.

Abstract

Recombinants between an adenovirus type 5 (Ad5) deletion mutant and the Ad12 DNA fragment containing early region 1 (E1) were isolated from cells cotransfected with the EcoRI-C fragment of Ad12 DNA and Ad5 dl312 (deletion in E1A) DNA (rcA) and from cells cotransfected with the SalI-C fragment of Ad12 DNA and Ad5 dl312 DNA (rcB). No recombinant was isolated from cells cotransfected with Ad5 dl313 (deletion in E1B) DNA and restriction fragments of Ad12 DNA. Both rcA and rcB are defective and able to replicate in human embryo kidney (HEK) and KB cells with complementation by dl312. Both rcA and rcB formed Ad12 T antigen g, but not T antigen f, in infected HEK and KB cells. In rcA- and rcB-infected cells, Ad5 E1B and Ad12 E1A genes are transcribed. Heteroduplex and size analyses of rcA-1 or rcB-1 DNA fragments hybridized with Ad12 DNA revealed that rcA-1 DNA has a deletion between 5 and 15 map units with an insertion of a portion of Ad12 DNA (10%) and that rcB-1 DNA has a deletion between 70 and 80 map units with an insertion of a portion of Ad12 DNA (10%). The transformed cell lines, RCAY and RCBY, were established after infection of rat 3Y1 cells with rcA and rcB, respectively. Both Ad5 and Ad12 DNA sequences are contained in these cells. In RCAY cells, Ad12 T antigen g is detected, but Ad12 T antigen f is not. In RCBY cells, both Ad12 T antigen g and f are detected. Only the Ad12 E1A gene is transcribed in RCAY cells, whereas Ad5 E1B, Ad12 E1A, and Ad12 E1B genes are transcribed in RCBY cells. In soft-agar cultures, RCBY cells form large colonies, whereas RCAY cells form only tiny colonies. RCBY cells form tumors as efficiently as 12WY cells in transplanted rats. RCAY cells formed tumors inefficiently. Ad5-transformed 5WY cells do not form tumors. These observations indicate that the efficient tumor formation by RCBY cells is dependent on the expression of the Ad12 E1A and E1B genes, whereas the inefficient tumor formation by RCAY cells is due to the expression of only the Ad12 E1A gene.

摘要

从用腺病毒12型(Ad12)DNA的EcoRI - C片段和腺病毒5型(Ad5)dl312(E1A缺失)DNA共转染的细胞(rcA)以及用Ad12 DNA的SalI - C片段和Ad5 dl312 DNA共转染的细胞(rcB)中分离出Ad5缺失突变体与包含早期区域1(E1)的Ad12 DNA片段之间的重组体。从用Ad5 dl313(E1B缺失)DNA和Ad12 DNA的限制性片段共转染的细胞中未分离出重组体。rcA和rcB均有缺陷,在人胚肾(HEK)和KB细胞中,在dl312的互补作用下能够复制。在感染的HEK和KB细胞中,rcA和rcB均形成Ad12 T抗原g,但不形成T抗原f。在rcA和rcB感染的细胞中,Ad5 E1B和Ad12 E1A基因被转录。用Ad12 DNA杂交的rcA - 1或rcB - 1 DNA片段的异源双链和大小分析表明,rcA - 1 DNA在5至15个图距单位之间有缺失,并插入了一部分Ad12 DNA(10%),而rcB - 1 DNA在70至80个图距单位之间有缺失,并插入了一部分Ad12 DNA(10%)。分别用rcA和rcB感染大鼠3Y1细胞后建立了转化细胞系RCAY和RCBY。这些细胞中都含有Ad5和Ad12 DNA序列。在RCAY细胞中,检测到Ad12 T抗原g,但未检测到Ad12 T抗原f。在RCBY细胞中,检测到Ad12 T抗原g和f。在RCAY细胞中仅转录Ad12 E1A基因,而在RCBY细胞中转录Ad� E1B、Ad12 E1A和Ad12 E1B基因。在软琼脂培养中,RCBY细胞形成大菌落,而RCAY细胞仅形成微小菌落。在移植大鼠中,RCBY细胞形成肿瘤的效率与12WY细胞一样高。RCAY细胞形成肿瘤的效率低。Ad5转化的5WY细胞不形成肿瘤。这些观察结果表明,RCBY细胞高效形成肿瘤依赖于Ad12 E1A和E1B基因的表达,而RCAY细胞形成肿瘤效率低是由于仅表达Ad12 E1A基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f1d/256896/eabddaed2465/jvirol00158-0366-a.jpg

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