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杆状病毒单链DNA结合蛋白LEF-3介导假定解旋酶P143的核定位。

A baculovirus single-stranded DNA binding protein, LEF-3, mediates the nuclear localization of the putative helicase P143.

作者信息

Wu Y, Carstens E B

机构信息

Department of Microbiology and Immunology, Queen's University, Kingston, Ontario, Canada.

出版信息

Virology. 1998 Jul 20;247(1):32-40. doi: 10.1006/viro.1998.9235.

Abstract

The intracellular localization of the baculovirus Autographa californica nuclear polyhedrosis virus p143 gene product (P143) was investigated by immunofluoresence staining of infected and transfected cells. As expected for a protein essential for viral DNA replication, under these conditions, P143 was localized to the nucleus. However, when a plasmid directing the synthesis of P143 from its own promoter was co-transfected with a plasmid expressing IE-1, P143 was found in the cytoplasm. Cotransfection of cells with a series of plasmids expressing viral genes sufficient for stimulation of plasmid replication resulted in nuclear localization of P143 suggesting that one of the gene products required for viral DNA replication may also assist nuclear localization of P143. Sequential deletion of various genes from this assay revealed that when the plasmid expressing LEF-3 was deleted from the mixture, P143 remained in the cytoplasm. Plasmids were constructed where the synthesis of LEF-3 and P143 were directed by the ie-1 promoter. When these plasmids were cotransfected, both LEF-3 and P143 colocalized to the nucleus suggesting that an important function of LEF-3 is intracellular trafficking of P143 and directing it to the nucleus.

摘要

通过对感染和转染细胞进行免疫荧光染色,研究了杆状病毒苜蓿银纹夜蛾核型多角体病毒p143基因产物(P143)的细胞内定位。作为病毒DNA复制所必需的一种蛋白质,在这些条件下,P143定位于细胞核,这是预期的结果。然而,当一个从其自身启动子指导P143合成的质粒与一个表达IE-1的质粒共转染时,P143出现在细胞质中。用一系列表达足以刺激质粒复制的病毒基因的质粒对细胞进行共转染,导致P143的核定位,这表明病毒DNA复制所需的基因产物之一可能也有助于P143的核定位。从该试验中依次缺失各种基因后发现,当混合物中缺失表达LEF-3的质粒时,P143仍留在细胞质中。构建了由ie-1启动子指导LEF-3和P143合成的质粒。当这些质粒共转染时,LEF-3和P143都共定位于细胞核,这表明LEF-3的一个重要功能是P143的细胞内运输并将其导向细胞核。

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