Pedersen-Lane J, Belfort M
Science. 1987 Jul 10;237(4811):182-4. doi: 10.1126/science.3037701.
The bacteriophage T4 nrdB gene, encoding nucleoside diphosphate reductase subunit B, contains a self-splicing group I intervening sequence. The nrdB intron was shown to be absent from the genomes of the closely related T-even phages T2 and T6. Evidence for variable intron distribution was provided by autocatalytic 32P-guanosine 5'-triphosphate labeling of T-even RNAs, DNA and RNA hybridization analyses, and DNA sequencing studies. The results indicate the nonessential nature of the intron in nrdB expression and phage viability. Furthermore, they suggest that either precise intron loss from T2 and T6 or lateral intron acquisition by T4 occurred since the evolution of these phages from a common ancestor. Intron movement in the course of T-even phage divergence raises provocative questions about the origin of these self-splicing elements in prokaryotes.
编码核苷二磷酸还原酶亚基B的噬菌体T4 nrdB基因含有一个自我剪接的I类居间序列。已证明密切相关的T偶数噬菌体T2和T6的基因组中不存在nrdB内含子。通过T偶数RNA的自动催化32P - 鸟苷5'-三磷酸标记、DNA和RNA杂交分析以及DNA测序研究,提供了可变内含子分布的证据。结果表明内含子在nrdB表达和噬菌体活力方面是非必需的。此外,这表明自这些噬菌体从共同祖先进化以来,要么T2和T6发生了精确的内含子丢失,要么T4发生了侧向内含子获得。T偶数噬菌体分化过程中的内含子移动引发了关于原核生物中这些自我剪接元件起源的有趣问题。