Ohtsubo H, Kumekawa N, Ohtsubo E
Institute of Molecular and Cellular Biosciences, University of Tokyo, Japan.
Genes Genet Syst. 1999 Jun;74(3):83-91. doi: 10.1266/ggs.74.83.
The 441-bp DNA segment in a PCR-amplified fragment from Oryza sativa cv. IR36 was found to have a sequence with features characteristic of LTRs of retroelements, which was named RIRE2 (Rice retroelement #2) and further analyzed. Cloning and sequencing analyses of the DNA segments connected to LTR-like sequence showed that RIRE2 has a long internal region almost 10 kb long that is flanked by LTR-like sequences. This internal region carries a primer binding site (PBS) and polypurine tract (PPT) which are necessary for cDNA synthesis of retroelements. The PBS sequence is complementary to the 3' end region of tRNA(Arg). The internal region has an rt gene homologous to that of gypsy-type retrotransposons, evidence that RIRE2 is indeed a retrotransposon related to gypsy from Drosophila. RIRE2 has an extra sequence more than 4 kb long in the region downstream of gag-pol. Phylogenetic analysis of the putative amino-acid sequences of the rt gene as well as the int gene showed that RIRE2 is related to a group of gypsy-type retrotransposons of a large size that include Grande1-4 of teosinte, Tat4-1 and Athila1-1 of Arabidopsis thaliana, and Cyclops-2 of pea, but distantly related to any other group of gypsy-type retrotransposons, including RIRE3 and RIRE8 of rice. RIRE2 and Grande1-4 had the highest homology in the gag-pol region, but the nucleotide sequences of the LTR regions differed. Both elements had significant homology in the middle area of the extra regions downstream of gag-pol, in which they had an open reading frame encoding a protein with no known function on the opposite strand from that coding for gag-pol.
在来自水稻品种IR36的PCR扩增片段中,发现一个441bp的DNA片段具有反转录元件长末端重复序列(LTR)的特征序列,将其命名为RIRE2(水稻反转录元件2号)并进一步分析。与LTR样序列相连的DNA片段的克隆和测序分析表明,RIRE2有一个近10kb长的长内部区域,两侧是LTR样序列。该内部区域带有引物结合位点(PBS)和多聚嘌呤序列(PPT),这是反转录元件cDNA合成所必需的。PBS序列与tRNA(Arg)的3'末端区域互补。内部区域有一个与gypsy型反转录转座子的rt基因同源的基因,这证明RIRE2确实是一个与果蝇gypsy相关的反转录转座子。RIRE2在gag-pol下游区域有一个超过4kb长的额外序列。对rt基因以及int基因的推测氨基酸序列进行系统发育分析表明,RIRE2与一组大型的gypsy型反转录转座子相关,包括玉米的Grande1 - 4、拟南芥的Tat4 - 1和Athila1 - 1以及豌豆的Cyclops - 2,但与任何其他gypsy型反转录转座子组关系较远,包括水稻的RIRE3和RIRE8。RIRE2和Grande1 - 4在gag-pol区域具有最高的同源性,但LTR区域的核苷酸序列不同。这两个元件在gag-pol下游额外区域的中间区域具有显著同源性,在该区域它们在与编码gag-pol的链相反的链上有一个编码未知功能蛋白质的开放阅读框。