Nagaki Kiyotaka, Neumann Pavel, Zhang Dongfen, Ouyang Shu, Buell C Robin, Cheng Zhukuan, Jiang Jiming
Department of Horticulture, University of Wisconsin-Madison, USA.
Mol Biol Evol. 2005 Apr;22(4):845-55. doi: 10.1093/molbev/msi069. Epub 2004 Dec 22.
The centromeric retrotransposon (CR) family in the grass species is one of few Ty3-gypsy groups of retroelements that preferentially transpose into highly specialized chromosomal domains. It has been demonstrated in both rice and maize that CRR (CR of rice) and CRM (CR of maize) elements are intermingled with centromeric satellite DNA and are highly concentrated within cytologically defined centromeres. We collected all of the CRR elements from rice chromosomes 1, 4, 8, and 10 that have been sequenced to high quality. Phylogenetic analysis revealed that the CRR elements are structurally diverged into four subfamilies, including two autonomous subfamilies (CRR1 and CRR2) and two nonautonomous subfamilies (noaCRR1 and noaCRR2). The CRR1/CRR2 elements contain all characteristic protein domains required for retrotransposition. In contrast, the noaCRR elements have different structures, containing only a gag or gag-pro domain or no open reading frames. The CRR and noaCRR elements share substantial sequence similarity in regions required for DNA replication and for recognition by integrase during retrotransposition. These data, coupled with the presence of young noaCRR elements in the rice genome and similar chromosomal distribution patterns between noaCRR1 and CRR1/CRR2 elements, suggest that the noaCRR elements were likely mobilized through the retrotransposition machinery from the autonomous CRR elements. Mechanisms of the targeting specificity of the CRR elements, as well as their role in centromere function, are discussed.
禾本科植物中的着丝粒逆转座子(CR)家族是少数优先转座到高度特化染色体区域的Ty3-gypsy逆转座子群体之一。在水稻和玉米中均已证实,CRR(水稻的CR)和CRM(玉米的CR)元件与着丝粒卫星DNA相互交织,并高度集中在细胞学定义的着丝粒内。我们从已高质量测序的水稻第1、4、8和10号染色体上收集了所有CRR元件。系统发育分析表明,CRR元件在结构上分为四个亚家族,包括两个自主亚家族(CRR1和CRR2)和两个非自主亚家族(noaCRR1和noaCRR2)。CRR1/CRR2元件包含逆转座所需的所有特征性蛋白质结构域。相比之下,noaCRR元件具有不同的结构,仅包含一个gag或gag-pro结构域或没有开放阅读框。CRR和noaCRR元件在DNA复制以及逆转座过程中整合酶识别所需的区域具有大量序列相似性。这些数据,再加上水稻基因组中存在年轻的noaCRR元件以及noaCRR1与CRR1/CRR2元件之间相似的染色体分布模式,表明noaCRR元件可能是通过自主CRR元件的逆转座机制被激活的。本文讨论了CRR元件的靶向特异性机制及其在着丝粒功能中的作用。