Tate W P, Poole E S, Dalphin M E, Major L L, Crawford D J, Mannering S A
Department of Biochemistry, University of Otago, Dunedin, New Zealand.
Biochimie. 1996;78(11-12):945-52. doi: 10.1016/s0300-9084(97)86716-8.
Wide ranging studies of the readthrough of translational stop codons within the last 25 years have suggested that the stop codon might be only part of the molecular signature for recognition of the termination signal. Such studies do not distinguish between effects on suppression and effects on termination, and so we have used a number of different approaches to deduce whether the stop signal is a codon with a context or an extended factor recognition element. A data base of natural termination sites from a wide range of organisms (148 organisms, approximately 40,000 sequences) shows a very marked bias in the bases surrounding the stop codon in the genes for all organisms examined, with the most dramatic bias in the base following the codon (+4). The nature of this base determines the efficiency of the stop signal in vivo, and in Escherichia coli this is reinforced by overexpressing the stimulatory factor, release factor 3. Strong signals, defined by their high relative rates of selecting the decoding release factors, are enhanced whereas weak signals respond relatively poorly. Site-directed cross-linking from the +1, and bases up to +6 but not beyond make close contact with the bacterial release factor-2. The translational stop signal is deduced to be an extended factor recognition sequence with a core element, rather than simply a factor recognition triplet codon influenced by context.
在过去25年里,对翻译终止密码子通读现象进行的广泛研究表明,终止密码子可能只是识别终止信号的分子特征的一部分。此类研究并未区分对抑制作用和对终止作用的影响,因此我们采用了多种不同方法来推断终止信号是具有上下文的密码子还是扩展的因子识别元件。来自多种生物(148种生物,约40000个序列)的自然终止位点数据库显示,在所研究的所有生物的基因中,终止密码子周围的碱基存在非常明显的偏向性,密码子之后的碱基(+4)偏向性最为显著。该碱基的性质决定了体内终止信号的效率,在大肠杆菌中,通过过表达刺激因子释放因子3可增强这种效率。由选择解码释放因子的高相对速率所定义的强信号会增强,而弱信号的反应则相对较差。从+1以及直至+6但不超过+6的碱基进行的定点交联与细菌释放因子-2紧密接触。由此推断,翻译终止信号是一个具有核心元件的扩展因子识别序列,而不仅仅是受上下文影响的因子识别三联体密码子。