Shrimali Rajeev K, Lobanov Alexey V, Xu Xue-Ming, Rao Mahadev, Carlson Bradley A, Mahadeo Dana C, Parent Carole A, Gladyshev Vadim N, Hatfield Dolph L
Molecular Biology of Selenium Section, Laboratory of Cancer Prevention, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Biochem Biophys Res Commun. 2005 Apr 1;329(1):147-51. doi: 10.1016/j.bbrc.2005.01.120.
Characterizing Sec tRNAs that decode UGA provides one of the most direct and easiest means of determining whether an organism possesses the ability to insert selenocysteine (Sec) into protein. Herein, we used a combination of two techniques, computational to identify Sec tRNA genes and RT-PCR to sequence the gene products, to unequivocally demonstrate that two widely studied, model protozoans, Dictyostelium discoideum and Tetrahymena thermophila, encode Sec tRNA in their genomes. The advantage of using both procedures is that computationally we could easily detect potential Sec tRNA genes and then confirm by sequencing that the Sec tRNA was present in the tRNA population, and thus the identified gene was not a pseudogene. Sec tRNAs from both organisms decode UGA. T. thermophila Sec tRNA, like all other sequenced Sec tRNAs, is 90 nucleotides in length, while that from D. discoideum is 91 nucleotides long making it the longest eukaryotic sequenced to date. Evolutionary analyses of known Sec tRNAs reveal the two forms identified herein are the most divergent eukaryotic Sec tRNAs thus far sequenced.
鉴定解码UGA的硒代半胱氨酸tRNA(Sec tRNA)是确定生物体是否具有将硒代半胱氨酸(Sec)插入蛋白质能力的最直接、最简单的方法之一。在此,我们结合了两种技术,即通过计算鉴定Sec tRNA基因,并通过逆转录聚合酶链反应(RT-PCR)对基因产物进行测序,以明确证明两种广泛研究的模式原生动物,盘基网柄菌和嗜热四膜虫,在其基因组中编码Sec tRNA。使用这两种方法的优点是,通过计算我们可以轻松检测潜在的Sec tRNA基因,然后通过测序确认Sec tRNA存在于tRNA群体中,因此所鉴定的基因不是假基因。来自这两种生物体的Sec tRNA都解码UGA。嗜热四膜虫的Sec tRNA与所有其他已测序的Sec tRNA一样,长度为90个核苷酸,而来自盘基网柄菌的Sec tRNA长度为91个核苷酸,使其成为迄今为止测序的最长的真核生物Sec tRNA。对已知Sec tRNA的进化分析表明,本文鉴定的两种形式是迄今为止测序的分歧最大的真核生物Sec tRNA。