Chung Thanh, Siol Oliver, Dingermann Theodor, Winckler Thomas
Institut für Pharmazeutische Biologie, Universität Frankfurt am Main, Frankfurt am Main, Germany.
Mol Cell Biol. 2007 Dec;27(24):8492-501. doi: 10.1128/MCB.01173-07. Epub 2007 Oct 8.
Mobile genetic elements that reside in gene-dense genomes face the problem of avoiding devastating insertional mutagenesis of genes in their host cell genomes. To meet this challenge, some Saccharomyces cerevisiae long terminal repeat (LTR) retrotransposons have evolved targeted integration at safe sites in the immediate vicinity of tRNA genes. Integration of yeast Ty3 is mediated by interactions of retrotransposon protein with the tRNA gene-specific transcription factor IIIB (TFIIIB). In the genome of the social amoeba Dictyostelium discoideum, the non-LTR retrotransposon TRE5-A integrates approximately 48 bp upstream of tRNA genes, yet little is known about how the retrotransposon identifies integration sites. Here, we show direct protein interactions of the TRE5-A ORF1 protein with subunits of TFIIIB, suggesting that ORF1p is a component of the TRE5-A preintegration complex that determines integration sites. Our results demonstrate that evolution has put forth similar solutions to prevent damage of diverse, compact genomes by different classes of mobile elements.
存在于基因密集型基因组中的移动遗传元件面临着避免对宿主细胞基因组中的基因造成毁灭性插入诱变的问题。为应对这一挑战,一些酿酒酵母长末端重复(LTR)逆转录转座子已进化出在紧邻tRNA基因的安全位点进行靶向整合的能力。酵母Ty3的整合是由逆转录转座子蛋白与tRNA基因特异性转录因子IIIB(TFIIIB)相互作用介导的。在社会变形虫盘基网柄菌的基因组中,非LTR逆转录转座子TRE5-A在tRNA基因上游约48 bp处整合,然而对于该逆转录转座子如何识别整合位点知之甚少。在这里,我们展示了TRE5-A ORF1蛋白与TFIIIB亚基之间的直接蛋白质相互作用,表明ORF1p是决定整合位点的TRE5-A整合前复合体的一个组成部分。我们的结果表明,进化已经提出了类似的解决方案,以防止不同类别的移动元件对多样的致密基因组造成损害。