Department of Pharmaceutical Chemistry, University of California San Francisco, San Francisco, California, United States of America.
PLoS One. 2011 Mar 29;6(3):e18263. doi: 10.1371/journal.pone.0018263.
Translation of Giardiavirus (GLV) mRNA is initiated at an internal ribosome entry site (IRES) in the viral transcript. The IRES localizes to a downstream portion of 5' untranslated region (UTR) and a part of the early downstream coding region of the transcript. Recent studies indicated that the IRES does not require a pre-initiation complex to initiate translation but may directly recruit the small ribosome subunit with the help of a number of trans-activating protein factors. A La autoantigen homologue in the viral host Giardia lamblia, GlLa, was proposed as one of the potential trans-activating factors based on its specific binding to GLV-IRES in vitro. In this study, we further elucidated the functional role of GlLa in GLV-IRES mediated translation in Giardia by knocking down GlLa with antisense morpholino oligo, which resulted in a reduction of GLV-IRES activity by 40%. An over-expression of GlLa in Giardia moderately stimulated GLV-IRES activity by 20%. A yeast inhibitory RNA (IRNA), known to bind mammalian and yeast La autoantigen and inhibit Poliovirus and Hepatitis C virus IRES activities in vitro and in vivo, was also found to bind to GlLa protein in vitro and inhibited GLV-IRES function in vivo. The C-terminal domain of La autoantigen interferes with the dimerization of La and inhibits its function. An over-expression of the C-terminal domain (200-348aa) of GlLa in Giardia showed a dominant-negative effect on GLV-IRES activity, suggesting a potential inhibition of GlLa dimerization. HA tagged GlLa protein was detected mainly in the cytoplasm of Giardia, thus supporting a primary role of GlLa in translation initiation in Giardiavirus.
贾第虫病毒(GLV)mRNA 的翻译起始于病毒转录本中的内部核糖体进入位点(IRES)。IRES 定位于 5'非翻译区(UTR)的下游部分和转录本早期下游编码区的一部分。最近的研究表明,IRES 不需要起始复合物即可启动翻译,但可能在许多转录激活蛋白因子的帮助下直接募集小核糖体亚基。病毒宿主贾第虫中的一种 La 自身抗原同源物 GlLa,因其在体外与 GLV-IRES 特异性结合而被提议为潜在的转录激活因子之一。在这项研究中,我们通过反义形态发生素寡核苷酸敲低 GlLa 进一步阐明了 GlLa 在 GLV-IRES 介导的贾第虫翻译中的功能作用,这导致 GLV-IRES 活性降低了 40%。在贾第虫中过表达 GlLa 可适度刺激 GLV-IRES 活性增加 20%。酵母抑制 RNA(IRNA),已知能结合哺乳动物和酵母 La 自身抗原,并抑制体外和体内脊髓灰质炎病毒和丙型肝炎病毒 IRES 的活性,也被发现能与 GlLa 蛋白结合,并抑制体内 GLV-IRES 功能。La 自身抗原的 C 端结构域干扰 La 的二聚化并抑制其功能。在贾第虫中过表达 GlLa 的 C 端结构域(200-348aa)显示对 GLV-IRES 活性具有显性负效应,表明 GlLa 二聚化可能受到抑制。HA 标记的 GlLa 蛋白主要在贾第虫的细胞质中检测到,因此支持 GlLa 在贾第虫病毒翻译起始中的主要作用。