Vallabhaneni Haritha, Fan-Minogue Hua, Bedwell David M, Farabaugh Philip J
Program in Molecular and Cell Biology, Department of Biological Sciences, University of Maryland Baltimore County, Baltimore,Maryland 21250, USA.
RNA. 2009 May;15(5):889-97. doi: 10.1261/rna.1508109. Epub 2009 Mar 27.
Ciliated protozoa of the genus Euplotes have undergone genetic code reassignment, redefining the termination codon UGA to encode cysteine. In addition, Euplotes spp. genes very frequently employ shifty stop frameshifting. Both of these phenomena involve noncanonical events at a termination codon, suggesting they might have a common cause. We recently demonstrated that Euplotes octocarinatus peptide release factor eRF1 ignores UGA termination codons while continuing to recognize UAA and UAG. Here we show that both the Tetrahymena thermophila and E. octocarinatus eRF1 factors allow efficient frameshifting at all three termination codons, suggesting that UGA redefinition also impaired UAA/UAG recognition. Mutations of the Euplotes factor restoring a phylogenetically conserved motif in eRF1 (TASNIKS) reduced programmed frameshifting at all three termination codons. Mutation of another conserved residue, Cys124, strongly reduces frameshifting at UGA while actually increasing frameshifting at UAA/UAG. We will discuss these results in light of recent biochemical characterization of these mutations.
真核草履虫属的纤毛虫经历了遗传密码重新分配,将终止密码子UGA重新定义为编码半胱氨酸。此外,真核草履虫属的基因非常频繁地使用移位终止密码子移码。这两种现象都涉及终止密码子处的非规范事件,表明它们可能有共同的原因。我们最近证明,八肋游仆虫肽释放因子eRF1忽略UGA终止密码子,同时继续识别UAA和UAG。在这里,我们表明嗜热四膜虫和八肋游仆虫的eRF1因子都允许在所有三个终止密码子处有效移码,这表明UGA重新定义也损害了UAA/UAG的识别。真核草履虫因子的突变恢复了eRF1中一个系统发育保守基序(TASNIKS),减少了所有三个终止密码子处的程序性移码。另一个保守残基Cys124的突变强烈降低了UGA处的移码,而实际上增加了UAA/UAG处的移码。我们将根据这些突变最近的生化特征来讨论这些结果。