Fabbri S, Fruscoloni P, Bufardeci E, Di Nicola Negri E, Baldi M I, Attardi D G, Mattoccia E, Tocchini-Valentini G P
EniChem, Istituto Guido Donegani SpA, Laboratori di Biotecnologie, 00015 Monterotondo, Rome, Italy.
Science. 1998 Apr 10;280(5361):284-6. doi: 10.1126/science.280.5361.284.
Accuracy in transfer RNA (tRNA) splicing is essential for the formation of functional tRNAs, and hence for gene expression, in both Eukaryotes and Archaea. The specificity for recognition of the tRNA precursor (pre-tRNA) resides in the endonuclease, which removes the intron by making two independent endonucleolytic cleavages. Although the eukaryal and archaeal enzymes appear to use different features of pre-tRNAs to determine the sites of cleavage, analysis of hybrid pre-tRNA substrates containing eukaryal and archaeal sequences, described here, reveals that the eukaryal enzyme retains the ability to use the archaeal recognition signals. This result indicates that there may be a common ancestral mechanism for recognition of pre-tRNA by proteins.
在真核生物和古细菌中,转运RNA(tRNA)剪接的准确性对于功能性tRNA的形成至关重要,因此对于基因表达也至关重要。tRNA前体(pre-tRNA)识别的特异性存在于核酸内切酶中,该酶通过进行两次独立的核酸内切裂解来去除内含子。尽管真核生物和古细菌的酶似乎利用pre-tRNA的不同特征来确定切割位点,但本文所述的对含有真核生物和古细菌序列的杂交pre-tRNA底物的分析表明,真核生物的酶保留了利用古细菌识别信号的能力。这一结果表明,蛋白质识别pre-tRNA可能存在共同的祖先机制。