Quirk S M, Bell-Pedersen D, Belfort M
Wadsworth Center for Laboratories and Research, New York State Department of Health, Albany 12201-0509.
Cell. 1989 Feb 10;56(3):455-65. doi: 10.1016/0092-8674(89)90248-1.
Intron mobility in the T-even phages has been demonstrated. Efficient nonreciprocal conversion of intron minus (In-) alleles to intron plus (In+) occurred for the td and sunY genes, but not for nrdB. Conversion to In+ was absolutely dependent on expression of the respective intron open reading frame (ORF). Introns were inserted at their cognate sites in an intronless phage genome via an RNA-independent, DNA-based, duplicative recombination event that was stimulated by exon homology. The td intron ORF product directs the endonucleolytic cleavage of DNA, targeting the site of intron integration. A 21 nucleotide deletion of the integration site abolished high frequency intron inheritance. These experiments provide a novel example of gene conversion in prokaryotes, while suggesting a molecular rationale for the inconsistent distribution of introns within highly conserved exon contexts of the T-even phage genomes.
T偶数噬菌体中的内含子迁移已得到证实。td和sunY基因发生了内含子减(In-)等位基因向内含子加(In+)的高效非 reciprocal 转换,但nrdB基因未发生。向In+的转换绝对依赖于各自内含子开放阅读框(ORF)的表达。内含子通过由外显子同源性刺激的RNA非依赖、基于DNA的重复重组事件,插入到无内含子噬菌体基因组的同源位点。td内含子ORF产物指导DNA的内切核酸酶切割,靶向内含子整合位点。整合位点的21个核苷酸缺失消除了高频内含子遗传。这些实验提供了原核生物中基因转换的一个新例子,同时为T偶数噬菌体基因组高度保守外显子背景内含子分布不一致提供了分子原理。