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在潜伏感染的淋巴母细胞样细胞中鉴定马立克氏病病毒核抗原。

Identification of Marek's disease virus nuclear antigen in latently infected lymphoblastoid cells.

作者信息

Wen L T, Tanaka A, Nonoyama M

机构信息

Department of Virology, Showa University Research Institute for Biomedicine, St. Petersburg, Florida 33716.

出版信息

J Virol. 1988 Oct;62(10):3764-71. doi: 10.1128/JVI.62.10.3764-3771.1988.

Abstract

A new Marek's disease virus (MDV) nuclear antigen (MDNA) was identified in two MDV-transformed T-lymphoblastoid cell lines, MKT-1 and MSB-1, derived from chickens bearing tumors induced by MDV. This MDNA was not detected in MSB-1 cells maintained in iododeoxyuridine, which activates the latent MDV genome. Moreover, it was not found in chicken embryo fibroblasts undergoing productive and cytolytic infection with MDV. Expression of MDNA is not related to strain pathogenicity in chickens, because chicken embryo fibroblasts productively infected with the pathogenic RBIB strain or the nonpathogenic CV-1 strain of MDV did not express this antigen. DNA-protein immunoprecipitation studies revealed that MDNA bound to two sites in the 190,00-base-pair (bp) MDV genome. One of these loci identified by MDNA obtained from MKT-1 and MSB-1 cells corresponded to a 476-bp segment within the short unique region of BamHI-A MDV DNA. A second locus located in a 280-bp segment within the short inverted repeat region of BamHI-A was also identified by MDNA from MSB-1 cells but not by MDNA obtained from MKT-1 cells. Analyses of the nucleotide sequence by DNase digestion showed that MDNA protected a 60-bp segment spanning a 22-bp palindromic sequence of the short unique region and a 103-bp sequence encompassing a 32-bp palindrome in the short inverted repeat region of BamHI-A MDV DNA.

摘要

在两个源自感染马立克氏病病毒(MDV)诱发肿瘤的鸡的MDV转化T淋巴母细胞系MKT - 1和MSB - 1中,鉴定出一种新的马立克氏病病毒核抗原(MDNA)。在维持于碘脱氧尿苷中的MSB - 1细胞中未检测到这种MDNA,碘脱氧尿苷可激活潜伏的MDV基因组。此外,在经历MDV增殖性和溶细胞性感染的鸡胚成纤维细胞中也未发现它。MDNA的表达与鸡的毒株致病性无关,因为用MDV的致病性RBIB毒株或非致病性CV - 1毒株进行增殖性感染的鸡胚成纤维细胞不表达这种抗原。DNA - 蛋白质免疫沉淀研究表明,MDNA与190,000碱基对(bp)的MDV基因组中的两个位点结合。从MKT - 1和MSB - 1细胞获得的MDNA鉴定出的其中一个位点对应于BamHI - A MDV DNA短独特区域内的一个476 - bp片段。MSB - 1细胞的MDNA还鉴定出位于BamHI - A短反向重复区域内一个280 - bp片段中的第二个位点,但MKT - 1细胞获得的MDNA未鉴定出该位点。通过DNase消化对核苷酸序列的分析表明,MDNA保护了一个60 - bp片段,该片段跨越BamHI - A MDV DNA短独特区域的一个22 - bp回文序列以及短反向重复区域内一个包含32 - bp回文的103 - bp序列。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9056/253520/5f5d42458608/jvirol00089-0233-a.jpg

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