Department of Biological Sciences, University at Albany, Albany, United States.
RNA Institute, University at Albany, Albany, United States.
Elife. 2018 Jun 15;7:e34268. doi: 10.7554/eLife.34268.
Group II introns are mobile ribozymes that are rare in bacterial genomes, often cohabiting with various mobile elements, and seldom interrupting housekeeping genes. What accounts for this distribution has not been well understood. Here, we demonstrate that Ll.LtrB, the group II intron residing in a relaxase gene on a conjugative plasmid from , inhibits its host gene expression and restrains the naturally cohabiting mobile element from conjugative horizontal transfer. We show that reduction in gene expression is mainly at the mRNA level, and results from the interaction between exon-binding sequences (EBSs) in the intron and intron-binding sequences (IBSs) in the mRNA. The spliced intron targets the relaxase mRNA and reopens ligated exons, causing major mRNA loss. Taken together, this study provides an explanation for the distribution and paucity of group II introns in bacteria, and suggests a potential force for those introns to evolve into spliceosomal introns.
内含子 II 是移动的核酶,在细菌基因组中很少见,通常与各种移动元件共存,很少打断管家基因。造成这种分布的原因尚不清楚。在这里,我们证明了 Ll.LtrB,一种位于来自 的一个可移动质粒的松弛酶基因中的内含子,抑制了其宿主基因的表达,并阻止了自然共存的移动元件进行可移动水平转移。我们表明,基因表达的减少主要发生在 mRNA 水平,这是由于内含子中的外显子结合序列 (EBS) 和 mRNA 中的内含子结合序列 (IBS) 之间的相互作用。剪接内含子靶向松弛酶 mRNA 并重新打开连接的外显子,导致大量 mRNA 丢失。总的来说,这项研究为内含子 II 在细菌中的分布和稀有性提供了一个解释,并为那些内含子进化为剪接体内含子提供了一个潜在的动力。