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整合于猫大颗粒淋巴瘤细胞中的猫白血病前病毒基因组的分子克隆

Molecular cloning of feline leukemia provirus genomes integrated in the feline large granular lymphoma cells.

作者信息

Matsumoto Y, Tsujimoto H, Fukasawa M, Hirota Y, Miura T, Hayami M, Goitsuka R, Ono K, Hasegawa A

机构信息

Department of Veterinary Internal Medicine, Faculty of Agriculture, University of Tokyo, Japan.

出版信息

Arch Virol. 1990;111(3-4):177-85. doi: 10.1007/BF01311052.

Abstract

Feline leukemia virus (FeLV) is a horizontally transmitted agent of the domestic cat which is known to be associated with wide spectrum of diseases of the hematopoietic system. In the present study, proviral DNAs of FeLV proviruses were examined in the tumor cells of natural killer cell lineage which is very rare in cats. In the chromosomal DNA of the tumor cells, 5 distinct bands corresponding to exogenous FeLV provirus genomes were detected by digestion with EcoRI which does not cut most FeLV isolates. Five clones of pLC1, pLC2, pLC3, pLC4, and pLC5 obtained from the 5 respective bands were analysed by restriction endonuclease mapping and Southern blot hybridization using gene-specific probes of FeLV. The results have clearly demonstrated that pLC4 and pLC5 contained large deletions in the pol and part of gag regions, while the full-length proviruses could be observed in pLC1 and pLC2. Furthermore, pLC3 contained part of a variant FeLV genome having an EcoRI site in its gag region. The molecular clones of defective and variant FeLV in this study may be useful for the further examination of tumorigenesis of large granular lymphoma in the cat.

摘要

猫白血病病毒(FeLV)是家猫的一种水平传播病原体,已知它与造血系统的多种疾病有关。在本研究中,对猫中非常罕见的自然杀伤细胞系肿瘤细胞中的FeLV前病毒DNA进行了检测。在用EcoRI消化肿瘤细胞的染色体DNA时,检测到5条与外源性FeLV前病毒基因组相对应的不同条带,EcoRI不会切割大多数FeLV分离株。从5条各自的条带中获得的5个pLC1、pLC2、pLC3、pLC4和pLC5克隆,使用FeLV的基因特异性探针通过限制性内切酶图谱分析和Southern印迹杂交进行分析。结果清楚地表明,pLC4和pLC5在pol和部分gag区域含有大片段缺失,而在pLC1和pLC2中可观察到全长前病毒。此外,pLC3含有部分变异的FeLV基因组,其gag区域有一个EcoRI位点。本研究中缺陷型和变异型FeLV的分子克隆可能有助于进一步研究猫大颗粒淋巴瘤的肿瘤发生。

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