Ichiyanagi Kenji, Beauregard Arthur, Belfort Marlene
New York State Department of Health, State University of New York, PO Box 22002, Albany, NY 12201-2002, USA.
Proc Natl Acad Sci U S A. 2003 Dec 23;100(26):15742-7. doi: 10.1073/pnas.2536659100. Epub 2003 Dec 12.
Group II introns, widely believed to be the ancestors of nuclear pre-mRNA introns, are catalytic RNAs found in bacteria, archaea, and eukaryotes. They are mobile genetic elements that move via an RNA intermediate. They retrohome to intronless alleles and retrotranspose to ectopic sites, aided by an intron-encoded protein with reverse transcriptase, maturase, and endonuclease activities. Many group II introns identified in bacteria reside on plasmid genomes rather than bacterial chromosomes, implying that plasmids are havens for these retroelements. This study demonstrates that almost one-fourth of retrotransposition events of the Ll.LtrB intron in Lactococcus lactis are into the plasmid donor. This level is more than twice that predicted based on target size and plasmid copy number relative to the chromosome. In particular, the fraction of such plasmid targeting events was elevated to more than one-third of retrotransposition events by mutation of the intron-encoded endonuclease, a situation that may resemble most bacterial group II introns, which lack the endonuclease. Target-site sequences on the plasmid are more relaxed than those on the chromosome, likely accounting for preferred integration into plasmid replicons. Furthermore, the direction of integration relative to promoters and origins of replication is consistent with group II intron retrotransposition into single-stranded DNA at replication forks. This work provides mechanistic rationales for the prevalence of group II introns in natural plasmid populations and underscores that targeting to plasmids, which are themselves mobile elements, could promote intron spread.
II类内含子被广泛认为是核前体mRNA内含子的祖先,是在细菌、古细菌和真核生物中发现的具有催化活性的RNA。它们是通过RNA中间体移动的可移动遗传元件。在具有逆转录酶、成熟酶和内切核酸酶活性的内含子编码蛋白的帮助下,它们反向归巢到无内含子的等位基因,并反向转移到异位位点。在细菌中鉴定出的许多II类内含子存在于质粒基因组而非细菌染色体上,这意味着质粒是这些反转录元件的避风港。本研究表明,乳酸乳球菌中Ll.LtrB内含子近四分之一的反转录事件发生在质粒供体中。这一水平是基于相对于染色体的靶标大小和质粒拷贝数预测值的两倍多。特别是,通过内含子编码的内切核酸酶突变,此类质粒靶向事件的比例提高到反转录事件的三分之一以上,这种情况可能类似于大多数缺乏内切核酸酶的细菌II类内含子。质粒上的靶位点序列比染色体上的更宽松,这可能是其优先整合到质粒复制子中的原因。此外,相对于启动子和复制起点的整合方向与II类内含子在复制叉处反向转录到单链DNA一致。这项工作为II类内含子在天然质粒群体中的普遍存在提供了机制依据,并强调靶向本身就是可移动元件的质粒可以促进内含子的传播。