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腺病毒感染细胞中剪接因子的组织反映了从早期到晚期转变过程中基因表达的变化。

Organization of splicing factors in adenovirus-infected cells reflects changes in gene expression during the early to late phase transition.

作者信息

Aspegren A, Rabino C, Bridge E

机构信息

Biomedical Center, Uppsala University, Uppsala, S-75123, Sweden.

出版信息

Exp Cell Res. 1998 Nov 25;245(1):203-13. doi: 10.1006/excr.1998.4264.

Abstract

The spatial distribution of splicing factors is temporally regulated during adenovirus (ad) infection. Here we focus on two splicing factor distribution patterns characteristic of ad-infected cells. During the intermediate phase splicing factors surround sites of viral DNA accumulation in regions of high transcriptional activity. This distribution appears as a series of interconnected rings when viewed by microscopy. We refer to cells with this staining pattern as "ring cells." We have previously shown that at late times after infection, splicing factors are present in discrete structures identified as enlarged interchromatin granules (IGs) that also contain spliced viral RNA. We refer to cells with this pattern as "cluster cells." We determined which steps in viral gene expression occurred in ring and cluster cells. We found that transcription and some splicing of viral late genes had occurred in ring cells. Late RNA was present at transcription sites in ring cells. Cluster cells contained spliced viral late RNA in nuclear IGs and in the cytoplasm. The presence of cluster cells in the infected culture was well correlated with the export of viral RNA to the cytoplasm. Cluster cells had synthesized late proteins. Our data show that the dynamic localization of splicing factors reflects changes in gene expression activity of the infected cell as it switches over to late gene expression.

摘要

在腺病毒(Ad)感染期间,剪接因子的空间分布受到时间调控。在此,我们聚焦于Ad感染细胞特有的两种剪接因子分布模式。在中间阶段,剪接因子围绕病毒DNA在高转录活性区域的积累位点。通过显微镜观察时,这种分布呈现为一系列相互连接的环。我们将具有这种染色模式的细胞称为“环细胞”。我们先前已表明,在感染后的晚期,剪接因子存在于被鉴定为扩大的染色质间颗粒(IGs)的离散结构中,这些颗粒也含有剪接后的病毒RNA。我们将具有这种模式的细胞称为“簇细胞”。我们确定了病毒基因表达的哪些步骤发生在环细胞和簇细胞中。我们发现,病毒晚期基因的转录和一些剪接在环细胞中发生。晚期RNA存在于环细胞的转录位点。簇细胞在核IGs和细胞质中含有剪接后的病毒晚期RNA。感染培养物中簇细胞的存在与病毒RNA向细胞质的输出密切相关。簇细胞已合成晚期蛋白质。我们的数据表明,剪接因子的动态定位反映了感染细胞在切换到晚期基因表达时基因表达活性的变化。

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