Gindullis F, Desel C, Galasso I, Schmidt T
Plant Molecular Cytogenetics Group, Institute of Crop Science and Plant Breeding, Christian Albrechts University of Kiel, 24118 Kiel, Germany.
Genome Res. 2001 Feb;11(2):253-65. doi: 10.1101/gr.162301.
In higher eukaryotes, the DNA composition of centromeres displays a high degree of variation, even between chromosomes of a single species. However, the long-range organization of centromeric DNA apparently follows similar structural rules. In our study, a comparative analysis of the DNA at centromeric regions of Beta species, including cultivated and wild beets, was performed using a set of repetitive DNA sequences. Our results show that these regions in Beta genomes have a complex structure and consist of variable repetitive sequences, including satellite DNA, Ty3-gypsy-like retrotransposons, and microsatellites. Based on their molecular characterization and chromosomal distribution determined by fluorescent in situ hybridization (FISH), centromeric repeated DNA sequences were grouped into three classes. By high-resolution multicolor-FISH on pachytene chromosomes and extended DNA fibers we analyzed the long-range organization of centromeric DNA sequences, leading to a structural model of a centromeric region of the wild beet species Beta procumbens. The chromosomal mutants PRO1 and PAT2 contain a single wild beet minichromosome with centromere activity and provide, together with cloned centromeric DNA sequences, an experimental system toward the molecular isolation of individual plant centromeres. In particular, FISH to extended DNA fibers of the PRO1 minichromosome and pulsed-field gel electrophoresis of large restriction fragments enabled estimations of the array size, interspersion patterns, and higher order organization of these centromere-associated satellite families. Regarding the overall structure, Beta centromeric regions show similarities to their counterparts in the few animal and plant species in which centromeres have been analyzed in detail.
在高等真核生物中,着丝粒的DNA组成表现出高度的变异性,即使在单个物种的染色体之间也是如此。然而,着丝粒DNA的长程组织显然遵循相似的结构规则。在我们的研究中,使用一组重复DNA序列对包括栽培甜菜和野生甜菜在内的甜菜属物种着丝粒区域的DNA进行了比较分析。我们的结果表明,甜菜基因组中的这些区域具有复杂的结构,由可变的重复序列组成,包括卫星DNA、Ty3-gypsy类逆转座子和微卫星。根据通过荧光原位杂交(FISH)确定的它们的分子特征和染色体分布,着丝粒重复DNA序列被分为三类。通过对粗线期染色体和延伸的DNA纤维进行高分辨率多色FISH,我们分析了着丝粒DNA序列的长程组织,从而得出了野生甜菜物种平卧甜菜着丝粒区域的结构模型。染色体突变体PRO1和PAT2包含一个具有着丝粒活性的单个野生甜菜小染色体,并与克隆的着丝粒DNA序列一起提供了一个用于分子分离单个植物着丝粒的实验系统。特别是,对PRO1小染色体的延伸DNA纤维进行FISH以及对大限制性片段进行脉冲场凝胶电泳,能够估计这些着丝粒相关卫星家族的阵列大小、散布模式和高级组织。就整体结构而言,甜菜着丝粒区域与其在少数已详细分析着丝粒的动植物物种中的对应区域相似。