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利什曼原虫RNA病毒感染细胞中一种短病毒转录本的鉴定。

Identification of a short viral transcript in Leishmania RNA virus-infected cells.

作者信息

Chung I K, Armstrong T C, Patterson J L

机构信息

Department of Microbiology and Molecular Genetics, Harvard Medical School, Boston, Massachusetts 02115.

出版信息

Virology. 1994 Feb;198(2):552-6. doi: 10.1006/viro.1994.1066.

Abstract

Certain strains of Leishmania guyanensis carry persistently infecting double-stranded RNA viruses. The viral polymerase has been shown to have both transcriptase and replicase activity. To date, only full-length RNA transcription of minus and plus strands have been reported. This report describes the synthesis of a 320 nt transcript which is complementary to the 3' end of the minus strand RNA. This plus-stranded short transcript was first detected in an in vitro polymerase assay. It was also detected in virus-infected Leishmania cells by a reverse transcription-polymerase chain reaction assay and by Northern analysis of infected Leishmania cell RNA.

摘要

某些圭亚那利什曼原虫菌株携带持续感染的双链RNA病毒。已证明该病毒聚合酶具有转录酶和复制酶活性。迄今为止,仅报道了负链和正链的全长RNA转录。本报告描述了一种320 nt转录本的合成,该转录本与负链RNA的3'末端互补。这种正链短转录本首先在体外聚合酶测定中被检测到。通过逆转录-聚合酶链反应测定以及对感染利什曼原虫细胞RNA的Northern分析,也在病毒感染的利什曼原虫细胞中检测到了它。

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