Zhong Jin, Lambowitz Alan M
Institute for Cellular and Molecular Biology, Department of Chemistry and Biochemistry, and Section of Molecular, Genetics and Microbiology, School of Biological Sciences, University ofTexas at Austin, Austin, TX 78712, USA.
EMBO J. 2003 Sep 1;22(17):4555-65. doi: 10.1093/emboj/cdg433.
The Lactococcus lactis Ll.LtrB group II intron uses a major retrohoming mechanism in which the excised intron RNA reverse splices into one strand of a DNA target site, while the intron-encoded protein uses a C-terminal DNA endonuclease domain to cleave the opposite strand and then uses the cleaved 3' end as a primer for reverse transcription of the inserted intron RNA. Here, experiments with mutant introns and target sites indicate that Ll.LtrB can retrohome without second-strand cleavage by using a nascent strand at a DNA replication fork as the primer for reverse transcription. This mechanism connecting intron mobility to target DNA replication may be used by group II intron species that encode proteins lacking the C-terminal DNA endonuclease domain and for group II intron retrotransposition to ectopic sites.
乳酸乳球菌Ll.LtrB II类内含子采用一种主要的归巢机制,即切除的内含子RNA反向剪接至DNA靶位点的一条链中,而内含子编码蛋白利用C端DNA内切酶结构域切割互补链,然后将切割后的3'端用作插入的内含子RNA逆转录的引物。在此,对突变内含子和靶位点的实验表明,Ll.LtrB可通过利用DNA复制叉处的新生链作为逆转录引物,在不进行第二链切割的情况下归巢。这种将内含子移动性与靶DNA复制相联系的机制,可能被编码缺乏C端DNA内切酶结构域蛋白的II类内含子种类所利用,也可用于II类内含子向异位位点的逆转座。