Mizuno Hiroshi, Wu Jianzhong, Kanamori Hiroyuki, Fujisawa Masaki, Namiki Nobukazu, Saji Shoko, Katagiri Satoshi, Katayose Yuichi, Sasaki Takuji, Matsumoto Takashi
National Institute of Agrobiological Sciences, 1-2, Kannondai 2-chome, Tsukuba, Ibaraki 305-8602, Japan.
Plant J. 2006 Apr;46(2):206-17. doi: 10.1111/j.1365-313X.2006.02684.x.
Telomeres, which are important for chromosome maintenance, are composed of long, repetitive DNA sequences associated with a variety of telomere-binding proteins. We characterized the organization and structure of rice telomeres and adjacent subtelomere regions on the basis of cytogenetic and sequence analyses. The length of the rice telomeres ranged from 5.1 to 10.8 kb, as revealed by both fibre-fluorescent in situ hybridization and terminal restriction-fragment assay. Physical maps of the chromosomal ends were constructed from a fosmid library. This facilitated sequencing of the telomere regions of chromosomes 1S, 2S, 2L, 6L, 7S, 7L and 8S. The resulting sequences contained conserved TTTAGGG telomere repeats, which indicates that the physical maps partly covered the telomere regions of the respective chromosome arms. These repeats were organized in the order of 5'-TTTAGGG-3' from the chromosome-specific region, except in chromosome 7S, in which seven inverted copies also existed in tandem array. Analysis of the telomere-flanking regions revealed the occurrence of deletions, insertions, or chromosome-specific substitutions of single nucleotides within the repeat sequences at the junction between the telomere and subtelomere. The sequences of the 500-kb regions of the seven chromosome ends were analysed in detail. A total of 598 genes were predicted in the telomeric regions. In addition, repetitive sequences derived from various kinds of retrotransposon were identified. No significant evidence for segmental duplication could be detected within or among the subtelomere regions. These results indicate that the rice chromosome ends are heterogeneous in both sequence and characterization.
端粒对于染色体的维持至关重要,它由与多种端粒结合蛋白相关的长链重复DNA序列组成。我们基于细胞遗传学和序列分析对水稻端粒及相邻的亚端粒区域的组织和结构进行了表征。纤维荧光原位杂交和末端限制片段分析均显示,水稻端粒的长度在5.1至10.8 kb之间。利用fosmid文库构建了染色体末端的物理图谱。这有助于对第1条短臂、第2条短臂、第2条长臂、第6条长臂、第7条短臂、第7条长臂和第8条短臂的端粒区域进行测序。所得序列包含保守的TTTAGGG端粒重复序列,这表明物理图谱部分覆盖了各染色体臂的端粒区域。这些重复序列从染色体特异性区域开始按5'-TTTAGGG-3'的顺序排列,但7号短臂染色体除外,该染色体中还存在7个串联排列的反向拷贝。对端粒侧翼区域的分析揭示了在端粒与亚端粒交界处的重复序列内存在缺失、插入或单核苷酸的染色体特异性替换。对7个染色体末端500 kb区域的序列进行了详细分析。在端粒区域共预测到598个基因。此外,还鉴定出了源自各种反转录转座子的重复序列。在亚端粒区域内或之间未检测到明显的片段重复证据。这些结果表明,水稻染色体末端在序列和特征上均具有异质性。