Ikeno M, Masumoto H, Okazaki T
Department of Molecular Biology, School of Science, Nagoya University, Japan.
Hum Mol Genet. 1994 Aug;3(8):1245-57. doi: 10.1093/hmg/3.8.1245.
The long-range organization of alphoid DNA arrays of human chromosome 21 was investigated using a mouse-human somatic cell hybrid. Two distinct long alphoid DNA arrays, the loci alpha 21-I and alpha 21-II, were identified in the centromere region of human chromosome 21. The alpha 21-I locus, composed of an array of 11 monomer repeat units (the 11 mer), was estimated to have a total length of 1.3 Mbp. CENP-B boxes, the binding sites of the centromere protein B (CENP-B), appeared in every other monomer unit in the 11 mer except for one place where two monomer units were repeated without any CENP-B box. The other locus, alpha 21-II, was found to be composed of alphoid subfamilies with low homology to the components of alpha 21-I locus. Five different alphoid clones presenting 32 monomer units in total were isolated from the alpha 21-II locus. Sequences of these monomer units diverged between 71-89% and no unit containing a CENP-B box was found. By analysis using two color FISH, the alpha 21-I was localized to the primary constriction, whereas the alpha 21-II site was located slightly to the short arm side. Furthermore, a combination of FISH and immunofluorescent staining indicated that the alpha 21-I site was co-localized and overlapped with the CREST centromere antigenic site on mitotic chromosomes and in interphase nuclei, while alpha 21-II was distributed broadly. Our data suggest that the locus alpha 21-I containing regularly spaced CENP-B boxes at high-frequency and the assembly site of the centromere antigens may be involved in common centromere function in both human and mouse cells.
利用小鼠 - 人杂种体细胞研究了人类21号染色体α卫星DNA阵列的长程组织。在人类21号染色体的着丝粒区域鉴定出两个不同的长α卫星DNA阵列,即α21 - I和α21 - II位点。α21 - I位点由11个单体重复单元(11聚体)的阵列组成,估计总长度为1.3 Mbp。着丝粒蛋白B(CENP - B)的结合位点CENP - B盒,出现在11聚体中每隔一个单体单元中,但有一处两个单体单元重复出现且没有任何CENP - B盒。另一个位点α21 - II,发现由与α21 - I位点成分同源性低的α卫星亚家族组成。从α21 - II位点分离出总共呈现32个单体单元的5个不同的α卫星克隆。这些单体单元的序列差异在71 - 89%之间,未发现含有CENP - B盒的单元。通过双色荧光原位杂交分析,α21 - I定位于主缢痕,而α21 - II位点位于短臂侧稍远处。此外,荧光原位杂交和免疫荧光染色相结合表明,α21 - I位点在有丝分裂染色体和间期核中与CREST着丝粒抗原位点共定位并重叠,而α21 - II分布广泛。我们的数据表明,含有高频规则间隔CENP - B盒的α21 - I位点以及着丝粒抗原的组装位点可能参与人类和小鼠细胞的共同着丝粒功能。