Huang Z M, Zang W Q, Yen T S
Department of Pathology, University of California School of Medicine, San Francisco, USA.
Virology. 1996 Mar 15;217(2):573-81. doi: 10.1006/viro.1996.0152.
The hepatitis B virus posttranscriptional regulatory element (PRE), which resides in the 3' region of the viral S transcripts, is important for the high-level expression of these mRNA species. We have previously shown that the PRE acts intranuclearly in cis to allow efficient export of intronless transcripts into the cytoplasm, in a manner that is independent of viral trans-acting factors. We here present data demonstrating that there are widely dispersed subelements in the PRE that are important for its function. All of these subelements bind, albeit with different affinities, to the same or similar host nuclear factor(s) containing two proteins, approximately 30 and 45 kDa in mass. The affinity of protein binding to a subelement is positively correlated with the ability of the subelement to activate intronless gene expression. Therefore, it appears that the PRE functions by having multiple binding sites for nuclear proteins that may be directly or indirectly involved in export of unspliced mRNA species.
乙型肝炎病毒转录后调控元件(PRE)位于病毒S转录本的3'区域,对这些mRNA种类的高水平表达至关重要。我们先前已表明,PRE在细胞核内顺式作用,以一种独立于病毒反式作用因子的方式,使无内含子转录本高效输出到细胞质中。我们在此展示的数据表明,PRE中存在广泛分散的亚元件,这些亚元件对其功能很重要。所有这些亚元件都能与包含两种蛋白质(质量约为30 kDa和45 kDa)的相同或相似宿主核因子结合,尽管结合亲和力不同。蛋白质与亚元件的结合亲和力与该亚元件激活无内含子基因表达的能力呈正相关。因此,PRE似乎是通过具有多个核蛋白结合位点来发挥功能的,这些核蛋白可能直接或间接参与未剪接mRNA种类的输出。