Tahara M, Aoki T, Suzuka S, Yamashita H, Tanaka M, Matsunaga S, Kokumai S
Faculty of Agriculture, Okayama University, 700-8530 Okayama, Okayama, Japan.
Mol Genet Genomics. 2004 Aug;272(1):116-27. doi: 10.1007/s00438-004-1044-2. Epub 2004 Jul 28.
A large number of plant retrotransposons have been characterized, but only three families ( Tnt1, Tto1 and Tos17) have been demonstrated to be transpositionally competent. We have used a novel approach to identify an active member of the Ty1- copia retrotransposon family with estimated 400 copies in the sweetpotato genome. Ty1- copia reverse transcriptase (RTase) sequences from the sweetpotato genome were analyzed, and a group of retrotransposon copies that probably arose by recent transposition events was identified and analyzed further. Transcripts containing long terminal repeats (LTRs) of this group were amplified from callus cDNA by the 3'RACE technique. Patterns of sequence-specific amplification polymorphism (S-SAP) of the LTR sequences in genomic DNA were compared between a normal plant and callus lines derived from it. In this way, a callus-specific S-SAP product was identified, which apparently resulted from the insertion of the retrotransposon detected by 3'RACE during cell culture. We conclude that our approach provides an effective way to identify active elements among the members of high-copy-number retrotransposon families.
大量植物反转录转座子已得到表征,但仅有三个家族(Tnt1、Tto1 和 Tos17)被证明具有转座活性。我们采用了一种新方法来鉴定甘薯基因组中估计有 400 个拷贝的 Ty1-copia 反转录转座子家族的一个活跃成员。对甘薯基因组中的 Ty1-copia 逆转录酶(RTase)序列进行了分析,鉴定出一组可能由近期转座事件产生的反转录转座子拷贝,并对其进行了进一步分析。通过 3'RACE 技术从愈伤组织 cDNA 中扩增出包含该组序列长末端重复序列(LTR)的转录本。比较了正常植株与其衍生的愈伤组织系基因组 DNA 中 LTR 序列的序列特异性扩增多态性(S-SAP)模式。通过这种方式,鉴定出一种愈伤组织特异性 S-SAP 产物,它显然是由细胞培养过程中 3'RACE 检测到的反转录转座子插入所致。我们得出结论,我们的方法为在高拷贝数反转录转座子家族成员中鉴定活跃元件提供了一种有效途径。