García-Martínez José, Martínez-Izquierdo José A
Departamento de Genética Molecular, Instituto de Biología Molecular de Barcelona, Barcelona, Spain.
Mol Biol Evol. 2003 May;20(5):831-41. doi: 10.1093/molbev/msg095. Epub 2003 Apr 2.
The study of Grande retrotransposon (RTN) variation reported here comprises the intrinsic element variability and the changes that element insertion provokes in the Zea genome, including its abundance among species. Sequence analysis of a defined long-terminal repeat (LTR) region from Grande RTN revealed a high level of sequence divergence since no identical sequences were found among the 65 clones examined that belong to different Zea species or maize inbred lines. Average diversity values within accessions ranged from 0.17 to 0.37 substitutions per nucleotide. Phylogenetic analysis revealed a lack of concordance between the phylogenetic tree obtained from LTR sequences and the conventional taxonomic tree, suggesting that different subfamilies of Grande elements existed before Zea speciation. When sequence-specific amplification polymorphism (SSAP) marker data, which combines genomic and RTN variation, are used, the derived trees reflect the established species phylogeny and allow, as well, differentiating among some maize lines. Finally, the evaluation of Grande abundance, using different element probes in all the Zea species but Z. luxurians, revealed around 5,700 copies per haploid genome in all the diploid species examined, indicating a similar expansion process of Grande in all the Zea genomes. This number of copies represents in all cases around a 3% of the genome, which implies that Grande RTN is an important component of the maize genome. The copy number ratio LTR/gag is around 2 in all the species analyzed, indicating that overwhelming majority of elements have internal region. Thus, mechanisms such as homologous recombination between LTRs of a single RTN, which would remove the internal region and one LTR, leaving behind a single recombinant LTR, seems not to be active in maize for Grande RTN.
本文报道的大反转录转座子(RTN)变异研究包括其内在元件变异性以及元件插入在玉米基因组中引发的变化,包括其在不同物种间的丰度。对大RTN特定长末端重复序列(LTR)区域的序列分析显示,由于在所检测的65个属于不同玉米物种或玉米自交系的克隆中未发现相同序列,因此序列分歧程度很高。各样本内的平均多样性值为每核苷酸0.17至0.37个替换。系统发育分析表明,从LTR序列获得的系统发育树与传统分类树之间缺乏一致性,这表明大元件的不同亚家族在玉米物种形成之前就已存在。当使用结合了基因组和RTN变异的序列特异性扩增多态性(SSAP)标记数据时,得到的树状图反映了已确立的物种系统发育关系,并且还能区分一些玉米品系。最后,在除繁茂玉米外的所有玉米物种中使用不同的元件探针评估大元件的丰度,结果显示在所检测的所有二倍体物种中,每个单倍体基因组约有5700个拷贝,这表明大元件在所有玉米基因组中的扩增过程相似。这个拷贝数在所有情况下约占基因组的3%,这意味着大RTN是玉米基因组的重要组成部分。在所有分析的物种中,LTR/gag的拷贝数比值约为2,这表明绝大多数元件都有内部区域。因此,单个RTN的LTR之间的同源重组等机制,这种机制会去除内部区域和一个LTR,只留下一个重组LTR,但对于玉米中的大RTN似乎并不活跃。