Zhang G, Zapp M L, Yan G, Green M R
Howard Hughes Medical Institute, University of Massachusetts Cancer Center, University of Massachusetts Medical Center, Worcester 01605, USA.
J Cell Biol. 1996 Oct;135(1):9-18. doi: 10.1083/jcb.135.1.9.
The Rev protein of human immunodeficiency virus type 1 (HIV-1) facilitates the nuclear export of unspliced and partially spliced viral RNAs. In the absence of Rev, these intron-containing HIV-1 RNAs are retained in the nucleus. The basis for nuclear retention is unclear and is an important aspect of Rev regulation. Here we use in situ hybridization and digital imaging microscopy to examine the intranuclear distributions of intron-containing HIV RNAs and to determine their spatial relationships to intranuclear structures. HeLa cells were transfected with an HIV-1 expression vector, and viral transcripts were localized using oligonucleotide probes specific for the unspliced or spliced forms of a particular viral RNA. In the absence of Rev, the unspliced viral RNAs were predominantly nuclear and had two distinct distributions. First, a population of viral transcripts was distributed as approximately 10-20 intranuclear punctate signals. Actinomycin D chase experiments indicate that these signals represent nascent transcripts. A second, stable population of viral transcripts was dispersed throughout the nucleoplasm excluding nucleoli. Rev promoted the export of this stable population of viral RNAs to the cytoplasm in a time-dependent fashion. Significantly, the distributions of neither the nascent nor the stable populations of viral RNAs coincided with intranuclear speckles in which splicing factors are enriched. Using splice-junction-specific probes, splicing of human beta-globin pre-mRNA occurred cotranscriptionally, whereas splicing of HIV-1 pre-mRNA did not. Taken together, our results indicate that the nucleolus and intranuclear speckles are not involved in Rev regulation, and provide further evidence that efficient splicing signals are critical for cotranscriptional splicing.
人类免疫缺陷病毒1型(HIV-1)的Rev蛋白促进未剪接和部分剪接的病毒RNA的核输出。在没有Rev的情况下,这些含有内含子的HIV-1 RNA会保留在细胞核中。核保留的基础尚不清楚,是Rev调节的一个重要方面。在这里,我们使用原位杂交和数字成像显微镜来检查含有内含子的HIV RNA在细胞核内的分布,并确定它们与核内结构的空间关系。用HIV-1表达载体转染HeLa细胞,并使用针对特定病毒RNA的未剪接或剪接形式的寡核苷酸探针来定位病毒转录本。在没有Rev的情况下,未剪接的病毒RNA主要存在于细胞核中,有两种不同的分布。首先,一群病毒转录本以大约10 - 20个核内点状信号的形式分布。放线菌素D追踪实验表明这些信号代表新生转录本。第二群稳定的病毒转录本分散在整个核质中,但不包括核仁。Rev以时间依赖性方式促进这群稳定的病毒RNA向细胞质的输出。值得注意的是,病毒RNA的新生群体和稳定群体的分布都与富含剪接因子的核内斑点不重合。使用剪接接头特异性探针,人β-珠蛋白前体mRNA的剪接是共转录发生的,而HIV-1前体mRNA的剪接则不是。综上所述,我们的结果表明核仁和核内斑点不参与Rev调节,并进一步证明有效的剪接信号对于共转录剪接至关重要。