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腺病毒12 E1基因转化的软琼脂集落形成大鼠细胞系的建立需要E4基因的表达。

Expression of the E4 gene is required for establishment of soft-agar colony-forming rat cell lines transformed by the adenovirus 12 E1 gene.

作者信息

Shiroki K, Hashimoto S, Saito I, Fukui Y, Fukui Y, Kato H, Shimojo H

出版信息

J Virol. 1984 Jun;50(3):854-63. doi: 10.1128/JVI.50.3.854-863.1984.

Abstract

Rat 3Y1 cells were transfected with recombinant gARC ( pSV2gpt carrying the adenovirus 12 early region 1 [E1] gene), and focus formation was observed in monolayer cultures after culture of cells in gpt-selective medium (Eagle medium containing 10% fetal calf serum, xanthine, thymidine, aminopterin, and mycophenolic acid) for 10 days, followed by focus formation. Transformed E1Y cell lines were then established from these foci. The E1Y cells were transformed morphologically similarly to cells transformed with intact adenovirus 12 DNA but formed no colonies in soft-agar culture and induced tumors in transplanted rats only after a long incubation period. For the establishment of completely transformed cells, 3Y1 cells were transformed with combinations of gARC , pE3 (pBR322 carrying the adenovirus 12 E3 gene), and gE4 ( pSV2gpt carrying the adenovirus 12 E4 gene) DNA. E1- 3Y cells (3Y1 cells transformed with gARC and pE3 DNA), E1- 4Y cells (3Y1 cells transformed with gARC and gE4 DNA), and E1-3- 4Y cells (3Y1 cells transformed with gARC , pE3 , and gE4 DNA) were established. These transformed cell lines were compared for growth in Eagle medium with 2 or 10% fetal calf serum, colony formation in soft-agar culture, and tumor growth in rats transplanted with the transformed cells. Several transformed cell lines of E1- 4Y and E1-3- 4Y cells showed colony formation in soft-agar culture and abundant expression of the E1B gene. T antigen f was seen by immunofluorescence as flecks in these cells, in which the E4 gene was transcribed, but was not seen in E1Y cells, suggesting that T antigen f was encoded by the E4 gene. The suggestion was confirmed by the observation that T antigen f was detected in COS-1 cells transfected singly with gE4 DNA by immunofluorescence with polyclonal and monoclonal antibodies. Transcription of the E4 gene was confirmed in gE4 -transfected COS-1 cells. T antigen f, one of the E4 gene products, was identified as a polypeptide of molecular weight 11,000 (E4- 11K ) by immunoprecipitation with monoclonal antibodies. The above results also suggest that expression of the E4 gene gives cells the advantage of forming colonies in soft-agar culture. A tendency was noticed for E1B gene expression to be enhanced by E4 gene expression. The relationship between enhancement of colony formation in soft-agar culture and enhancement of E1B gene expression is discussed.

摘要

用重组gARC(携带腺病毒12早期区域1 [E1]基因的pSV2gpt)转染大鼠3Y1细胞,将细胞在gpt选择培养基(含有10%胎牛血清、黄嘌呤、胸腺嘧啶核苷、氨基蝶呤和霉酚酸的伊格尔培养基)中培养10天,随后观察单层培养物中的集落形成。然后从这些集落建立转化的E1Y细胞系。E1Y细胞在形态上与用完整腺病毒12 DNA转化的细胞相似,但在软琼脂培养中不形成集落,并且仅在长时间孵育后才在移植的大鼠中诱导肿瘤。为了建立完全转化的细胞,用gARC、pE3(携带腺病毒12 E3基因的pBR322)和gE4(携带腺病毒12 E4基因的pSV2gpt)DNA的组合转化3Y1细胞。建立了E1 - 3Y细胞(用gARC和pE3 DNA转化的3Y1细胞)、E1 - 4Y细胞(用gARC和gE4 DNA转化的3Y1细胞)和E1 - 3 - 4Y细胞(用gARC、pE3和gE4 DNA转化的3Y1细胞)。比较这些转化细胞系在含有2%或10%胎牛血清的伊格尔培养基中的生长情况、在软琼脂培养中的集落形成以及在移植了转化细胞的大鼠中的肿瘤生长情况。几个E1 - 4Y和E1 - 3 - 4Y细胞的转化细胞系在软琼脂培养中显示出集落形成以及E1B基因的丰富表达。通过免疫荧光在这些细胞中观察到T抗原f呈斑点状,其中E4基因被转录,但在E1Y细胞中未观察到,这表明T抗原f由E4基因编码。通过用多克隆和单克隆抗体进行免疫荧光观察,在单独用gE4 DNA转染的COS - 1细胞中检测到T抗原f,证实了这一推测。在gE4转染的COS - 1细胞中证实了E4基因的转录。通过用单克隆抗体进行免疫沉淀,将E4基因产物之一T抗原f鉴定为分子量为11,000的多肽(E4 - 11K)。上述结果还表明E4基因的表达赋予细胞在软琼脂培养中形成集落的优势。注意到E4基因表达有增强E1B基因表达的趋势。讨论了软琼脂培养中集落形成的增强与E1B基因表达增强之间的关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99c1/255746/d3d83589b5f6/jvirol00135-0197-a.jpg

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