Assum G, Fink T, Steinbeisser T, Fisel K J
Abteilung Humangenetik, Universität Ulm, Germany.
Hum Genet. 1993 Jun;91(5):489-95. doi: 10.1007/BF00217778.
By screening total human DNA with probes derived from the small polydisperse circular (spc) DNA fraction of cultured human cells, we identified three clones that carry long stretches of beta-satellite DNA. Further experiments have shown that the three sequences belong to at least two different beta-satellite subfamilies, which are characterized by different higher order subunits. Members of one of these subfamilies are located in the cytological satellites of all acrocentric chromosomes, whereas members of another are located on the short arms of the acrocentrics on both sides of the stalk regions and also in the centromeric regions of chromosomes 1 and 9. This is the first time that beta-satellite sequences obtained from the spcDNA of human cells have been assigned to beta-satellite subfamilies that are organized as long arrays of tandemly arranged higher order monomers. This indicates that beta-satellite sequences can be excised from their chromosomal loci via intrastrand-recombination processes.
通过用源自培养的人类细胞的小多分散环状(spc)DNA片段的探针筛选人类总DNA,我们鉴定出三个携带长片段β卫星DNA的克隆。进一步的实验表明,这三个序列至少属于两个不同的β卫星亚家族,它们以不同的高阶亚基为特征。其中一个亚家族的成员位于所有近端着丝粒染色体的细胞学卫星中,而另一个亚家族的成员则位于近端着丝粒染色体短臂的柄区域两侧以及1号和9号染色体的着丝粒区域。这是首次将从人类细胞的spcDNA获得的β卫星序列分配到以串联排列的高阶单体长阵列形式组织的β卫星亚家族中。这表明β卫星序列可以通过链内重组过程从其染色体位点切除。