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首页> 外文期刊>Genes & Genetic Systems >New transposable elements identified as insertions in rice transposon Tnr1
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New transposable elements identified as insertions in rice transposon Tnr1

机译:鉴定为水稻转座子Tnr1中插入的​​新转座因子

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摘要

Tnr1 (235 bp long) is a transposable element in rice. Polymerase chain reactions (PCRs) done with a primer(s) that hybridizes to terminal inverted repeat sequences (TIRs) of Tnr1 detected new Tnr1 members with one or two insertions in rice genomes. Six identified insertion sequences (Tnr4, Tnr5, Tnr11, Tnr12,Tnr13 and RIRE9) did not have extensive homology to known transposable elements, rather they had structural features characteristic of transposable elements. Tnr4 (1767 bp long) had imperfect 64-bp TIRs and appeared to generate duplication of a 9-bp sequence at the target site. However, the TIR sequences were not homologous to those of known transposable elements, indicative that Tnr4 is a new transposable element. Tnr5 (209 bp long) had imperfect 46-bp TIRs and appeared to generate duplication of sequence TTA like that of some elements of the Tourist family. Tnr11 (811 bp long) had 73-bp TIRs with significant homology to those of Tnr1 and Stowaway and appeared to generate duplication of sequence TA, indicative that Tnr11 is a transposable element of the Tnr1/Stowaway family. Tnr12 (2426 bp long) carried perfect 9-bp TIRs, which began with 5'-CACTA--3' from both ends and appeared to generate duplication of a 3-bp target sequence, indicative that Tnr12 is a transposable element of the En/Spm family. Tnr13 (347 bp long) had 31-bp TIRs and appeared to generate duplication of an 8-bp target sequence. Two sequences, one the transposon-like element Crackle, had partial homology in the Tnr13 ends. All five insertions appear to be defective elements derived from autonomous ones encoding the transposase gene. All had characteristic tandem repeat sequences which may be recognized by transposase. The sixth insertion sequence, named RIRE9 (3852 bp long), which begins with 5'-TG--3'; and ends with 5'--CA-3', appeared to generate duplication of a 5-bp target sequence. These and other structural features indicate that this insertion is a solo LTR (long terminal repeat) of a retrotransposon. The transposable elements described above could be identified as insertions into Tnr1, which do not deleteriously affect the growth of rice cells.
机译:Tnr1(长235 bp)是水稻中的转座因子。用与Tnr1的末端反向重复序列(TIR)杂交的引物进行的聚合酶链反应(PCR)检测到水稻基因组中有一个或两个插入的新Tnr1成员。六个已鉴定的插入序列(Tnr4,Tnr5,Tnr11,Tnr12,Tnr13和RIRE9)与已知的转座因子没有广泛的同源性,而是具有转座因子的结构特征。 Tnr4(长1767 bp)具有不完善的64 bp TIR,并且似乎在目标位点产生9 bp序列的重复。但是,TIR序列与已知的转座因子的序列不同源,表明Tnr4是新的转座因子。 Tnr5(长209 bp)具有不完善的46 bp TIR,并且似乎会产生序列TTA的重复,就像游客家族的某些元素一样。 Tnr11(长811 bp)具有73 bp的TIR,与Tnr1和Stowaway具有显着同源性,并且似乎产生了序列TA的重复,这表明Tnr11是Tnr1 / Stowaway家族的转座因子。 Tnr12(长2426 bp)带有完美的9 bp TIR,其两端均以5'-CACTA--3'开头,似乎产生了3 bp的靶序列重复,这表明Tnr12是En的转座因子/ Spm家庭。 Tnr13(长347 bp)具有31 bp的TIR,似乎重复了8 bp的靶序列。有两个序列,一个为转座子样元件“裂纹”,在Tnr13末端具有部分同源性。所有五个插入物似乎都是源自编码转座酶基因的自主元件的缺陷元件。全部具有可被转座酶识别的特征性串联重复序列。第六个插入序列,名为RIRE9(长3852 bp),从5'-TG--3'开始;并以5'-CA-3'结尾,似乎产生了5bp靶序列的重复。这些和其他结构特征表明该插入是反转录转座子的单独LTR(长末端重复)。可以将上述转座因子识别为插入Tnr1中,不会对水稻细胞的生长产生有害影响。

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