Wu Jianzhong, Yamagata Harumi, Hayashi-Tsugane Mika, Hijishita Saori, Fujisawa Masaki, Shibata Michie, Ito Yukiyo, Nakamura Mari, Sakaguchi Miyuki, Yoshihara Rie, Kobayashi Harumi, Ito Kazue, Karasawa Wataru, Yamamoto Mayu, Saji Shoko, Katagiri Satoshi, Kanamori Hiroyuki, Namiki Nobukazu, Katayose Yuichi, Matsumoto Takashi, Sasaki Takuji
Rice Genome Research Program, National Institute of Agrobiological Sciences/Institute of the Society for Techno-Inovation of Agriculture, Forestry, and Fisheries, Tsukuba, Ibaraki 305-8602, Japan.
Plant Cell. 2004 Apr;16(4):967-76. doi: 10.1105/tpc.019273. Epub 2004 Mar 22.
Understanding the organization of eukaryotic centromeres has both fundamental and applied importance because of their roles in chromosome segregation, karyotypic stability, and artificial chromosome-based cloning and expression vectors. Using clone-by-clone sequencing methodology, we obtained the complete genomic sequence of the centromeric region of rice (Oryza sativa) chromosome 8. Analysis of 1.97 Mb of contiguous nucleotide sequence revealed three large clusters of CentO satellite repeats (68.5 kb of 155-bp repeats) and >220 transposable element (TE)-related sequences; together, these account for approximately 60% of this centromeric region. The 155-bp repeats were tandemly arrayed head to tail within the clusters, which had different orientations and were interrupted by TE-related sequences. The individual 155-bp CentO satellite repeats showed frequent transitions and transversions at eight nucleotide positions. The 40 TE elements with highly conserved sequences were mostly gypsy-type retrotransposons. Furthermore, 48 genes, showing high BLAST homology to known proteins or to rice full-length cDNAs, were predicted within the region; some were close to the CentO clusters. We then performed a genome-wide survey of the sequences and organization of CentO and RIRE7 families. Our study provides the complete sequence of a centromeric region from either plants or animals and likely will provide insight into the evolutionary and functional analysis of plant centromeres.
由于真核生物着丝粒在染色体分离、核型稳定性以及基于人工染色体的克隆和表达载体中发挥作用,了解其组织形式具有重要的基础意义和应用价值。我们采用逐个克隆的测序方法,获得了水稻(Oryza sativa)第8号染色体着丝粒区域的完整基因组序列。对1.97 Mb连续核苷酸序列的分析揭示了三个大的CentO卫星重复序列簇(68.5 kb的155 bp重复序列)和超过220个与转座元件(TE)相关的序列;这些序列总共约占该着丝粒区域的60%。155 bp的重复序列在簇内首尾串联排列,簇具有不同的方向,并被与TE相关的序列打断。单个155 bp的CentO卫星重复序列在八个核苷酸位置频繁发生转换和颠换。40个具有高度保守序列的TE元件大多是gypsy型逆转座子。此外,在该区域预测到48个与已知蛋白质或水稻全长cDNA具有高度BLAST同源性的基因;其中一些靠近CentO簇。然后,我们对CentO和RIRE7家族的序列和组织进行了全基因组调查。我们的研究提供了来自植物或动物的着丝粒区域的完整序列,可能会为植物着丝粒的进化和功能分析提供见解。