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感染马立克氏病病毒的网状内皮组织增殖病病毒转化的禽T淋巴细胞样细胞系的特性分析

Characterization of reticuloendotheliosis virus-transformed avian T-lymphoblastoid cell lines infected with Marek's disease virus.

作者信息

Pratt W D, Morgan R W, Schat K A

机构信息

Department of Avian and Aquatic Animal Medicine, College of Veterinary Medicine, Cornell University, Ithaca, New York 14853-6401.

出版信息

J Virol. 1992 Dec;66(12):7239-44. doi: 10.1128/JVI.66.12.7239-7244.1992.

DOI:10.1128/JVI.66.12.7239-7244.1992
PMID:1279200
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC240427/
Abstract

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.

摘要

在感染了马立克氏病病毒(MDV)的网状内皮组织增生症病毒转化的禽T淋巴细胞样细胞系RECC-CU91中,对MDV转录本和蛋白质产物的表达进行了研究。通过用32P标记的BamHI MDV DNA文库的BamHI-H和-B片段进行Southern杂交,证实了在重命名为RECC-CU210的超感染细胞系中存在MDV。对RECC-CU210中由MDV基因组的内部重复长片段(IRL)、内部重复短片段(IRS)和独特短片段(US)区域编码的MDV特异性RNA转录本的表达进行检测,发现了两条大小分别为0.6和0.7 kb的小转录本。这些转录本分别定位到IRL和IRS区域。相比之下,通过用MDV的BamHI-A片段转染CU210而得到的RECC-CU211,从IRL、IRS和US区域表达了另外九条转录本。CU211而非CU210还表达了一种由40、38和24 kDa多肽组成的复合物,单克隆抗体将其鉴定为MDV特异性磷蛋白。38 kDa的磷蛋白可能是pp38,一种早期病毒蛋白,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片段内的基因激活了许多位于MDV基因组IRL区域内的基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32ba/240427/47c13eb7be8a/jvirol00043-0418-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32ba/240427/c5444c1d29c1/jvirol00043-0417-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32ba/240427/eed69b0a85cd/jvirol00043-0417-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32ba/240427/7f6b31076928/jvirol00043-0418-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32ba/240427/47c13eb7be8a/jvirol00043-0418-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32ba/240427/c5444c1d29c1/jvirol00043-0417-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32ba/240427/eed69b0a85cd/jvirol00043-0417-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32ba/240427/7f6b31076928/jvirol00043-0418-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32ba/240427/47c13eb7be8a/jvirol00043-0418-b.jpg

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