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FBR-小鼠骨肉瘤病毒复合体的特性:FBR-MuSV编码一种源自FOS的癌基因。

Characterization of the FBR-murine osteosarcoma virus complex: FBR-MuSV encodes a FOS-derived oncogene.

作者信息

Michiels L, Maisin J R, Pedersen F S, Merregaert J

出版信息

Int J Cancer. 1984 Apr 15;33(4):511-7. doi: 10.1002/ijc.2910330415.

DOI:10.1002/ijc.2910330415
PMID:6323327
Abstract

The FBR murine osteosarcoma virus complex, isolated from a radiation-induced osteosarcoma of an X/Gf mouse causes the rapid appearance of osteosarcomas in newborn mice and transforms fibroblasts in vitro. The two components of the FBR-viral complex have been isolated separately in tissue culture: FBR-MuLV by end-point dilution and FBR-MuSV by the establishment of mouse [FBR-NP 117 (NIH 3T3)] and rat non-producer cell lines [FBR-NP415 (REF)]. The host range and RNase Tl fingerprint analysis of FBR-MuLV demonstrated a pattern closely related to, but distinguishable from, Akv-MuLV. Transformed cells from both mice and rats contain a rescuable FBR-MuSV genome. These pseudotypes produce foci in tissue culture and induce osteosarcomas in susceptible mouse strains. An FBR-MuSV (FBR-MuLV) cDNA probe detects a 5.2 kb HindIII and a 9.5 kb EcoRI FBR-MuSV-specific fragment in FBR-MuSV-transformed non-producer rat cells. The same fragments hybridized with a fos specific probe, demonstrating that FBR-provirus contains a c-fos-derived onc-gene.

摘要

从一只X/Gf小鼠的辐射诱导骨肉瘤中分离出的FBR鼠骨肉瘤病毒复合体,可使新生小鼠迅速出现骨肉瘤,并在体外转化成纤维细胞。FBR病毒复合体的两个组分已在组织培养中分别分离出来:通过终点稀释法分离出FBR-MuLV,通过建立小鼠[FBR-NP 117(NIH 3T3)]和大鼠非生产细胞系[FBR-NP415(REF)]分离出FBR-MuSV。FBR-MuLV的宿主范围和核糖核酸酶Tl指纹分析显示出一种与Akv-MuLV密切相关但又可区分的模式。来自小鼠和大鼠的转化细胞都含有可拯救的FBR-MuSV基因组。这些假型在组织培养中产生病灶,并在易感小鼠品系中诱发骨肉瘤。一个FBR-MuSV(FBR-MuLV)cDNA探针在FBR-MuSV转化的非生产大鼠细胞中检测到一个5.2 kb的HindIII和一个9.5 kb的EcoRI FBR-MuSV特异性片段。相同的片段与一个fos特异性探针杂交,表明FBR前病毒含有一个源自c-fos的致癌基因。

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Characterization of the FBR-murine osteosarcoma virus complex: FBR-MuSV encodes a FOS-derived oncogene.FBR-小鼠骨肉瘤病毒复合体的特性:FBR-MuSV编码一种源自FOS的癌基因。
Int J Cancer. 1984 Apr 15;33(4):511-7. doi: 10.1002/ijc.2910330415.
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Deletion of the gag region from FBR murine osteosarcoma virus does not affect its enhanced transforming activity.从FBR小鼠骨肉瘤病毒中删除gag区域不会影响其增强的转化活性。
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Transfer of murine leukaemia and murine sarcoma virus genetic information by transfection with isolated metaphase chromosomes.通过分离中期染色体转染传递小鼠白血病病毒和小鼠肉瘤病毒遗传信息
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In vitro induction of osteosarcomalike lesion by transformation of differentiating skeletal precursor cells with FBR murine osteosarcoma virus.
Calcif Tissue Int. 1987 Oct;41(4):208-17. doi: 10.1007/BF02555240.

引用本文的文献

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Myristylation of FBR v-fos dictates the differentiation pathways in malignant osteosarcoma.FBR v-fos的肉豆蔻酰化决定了恶性骨肉瘤的分化途径。
J Cell Biol. 1996 Oct;135(2):457-67. doi: 10.1083/jcb.135.2.457.
2
Biochemical characterization of a virus-induced osteosarcoma-like osseous lesion in vitro.病毒诱导的骨肉瘤样骨病变的体外生化特征
Calcif Tissue Int. 1989 Oct;45(4):232-42. doi: 10.1007/BF02556043.
3
Effects of leukemogenic retroviruses on condylar cartilage in vitro: an ultrastructural study.致白血病逆转录病毒对髁突软骨的体外影响:一项超微结构研究。
Calcif Tissue Int. 1989 Jan;44(1):25-35. doi: 10.1007/BF02556237.