首页> 美国卫生研究院文献>Journal of Virology >Characterization of reticuloendotheliosis virus-transformed avian T-lymphoblastoid cell lines infected with Mareks disease virus.
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Characterization of reticuloendotheliosis virus-transformed avian T-lymphoblastoid cell lines infected with Mareks disease virus.

机译:网状内皮细胞病病毒转化的感染了马立克氏病病毒的禽类T淋巴母细胞系的特征。

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摘要

The expression of Marek's disease virus (MDV) transcripts and protein products was investigated in reticuloendotheliosis virus-transformed avian T-lymphoblastoid cell line RECC-CU91, which was superinfected with MDV. The presence of MDV in the superinfected cell line, renamed RECC-CU210, was demonstrated by Southern hybridization with 32P-labeled BamHI-H and -B fragments of the BamHI MDV DNA library. Examination of RECC-CU210 for the expression of MDV-specific RNA transcripts encoded by the internal repeat long (IRL), internal repeat short (IRS), and unique short (US) regions of the MDV genome revealed two small transcripts of 0.6 and 0.7 kb. These transcripts were mapped to the IRL and IRS regions, respectively. In contrast, RECC-CU211, which was developed through transfection of CU210 with the BamHI-A fragment of MDV, expressed an additional nine transcripts from the IRL, IRS, and US regions. CU211 but not CU210 also expressed a complex of polypeptides of 40, 38, and 24 kDa, identified by monoclonal antibodies as MDV-specific phosphoproteins. The 38-kDa phosphoprotein is likely to be pp38, an early viral protein that maps within the IRL region of the MDV genome. These findings suggest that genes located within the transfected BamHI-A fragment transactivated a number of genes located in the IRL region of the MDV genome.
机译:研究了马立克氏病病毒(MDV)转录本和蛋白质产物在网状内皮细胞病病毒转化的禽T淋巴母细胞系RECC-CU91中的表达。通过与BamHI MDV DNA文库的32P标记的BamHI-H和-B片段进行Southern杂交,证明了超级感染的细胞系MDV的存在(重命名为RECC-CU210)。对RECC-CU210的MDV基因组的内部重复长(IRL),内部重复短(IRS)和唯一短(US)区域编码的MDV特异性RNA转录表达进行检查,发现两个小转录本,分别为0.6和0.7 kb。这些成绩单分别映射到IRL和IRS区域。相反,通过用MDV的BamHI-A片段转染CU210而开发的RECC-CU211表达了来自IRL,IRS和美国地区的另外9个转录本。 CU211但不表达CU210也表达40、38和24 kDa的多肽复合物,通过单克隆抗体鉴定为MDV特异性磷蛋白。 38 kDa的磷蛋白很可能是pp38,它是一种早期病毒蛋白,可定位于MDV基因组的IRL区域内。这些发现表明,位于转染的BamHI-A片段内的基因使位于MDV基因组的IRL区域中的许多基因转活化。

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