Christie N T, Sen P, Costa M
Institute of Environmental Medicine, New York University Medical Center, NY 10016.
Biol Met. 1988;1(1):43-50. doi: 10.1007/BF01128016.
Prior studies have shown a preferential decondensation (or fragmentation) of the heterochromatic long arm of the X chromosome of Chinese hamster ovary cells when treated with carcinogenic crystalline NiS particles (crNiS). In this report, we show that the heterochromatic regions of mouse chromosomes are also more frequently involved in aberrations than euchromatic regions, although the heterochromatin in mouse cells is restricted to centromeric regions. We also present the karyotypic analyses of four cell lines derived from tumors induced by leg muscle injections of crystalline nickel sulfide which have been analyzed to determine whether heterochromatic chromosomal regions are preferentially altered in the transformed genotypes. Common to all cell lines was the presence of minichromosomes, which are acrocentric chromosomes smaller than chromosome 19, normally the smallest chromosome of the mouse karyotype. The minichromosomes were present in a majority of cells of each line although the morphology of this extra chromosome varied significantly among the cell lines. C-banding revealed the presence of centromeric DNA and thus these minichromosomes may be the result of chromosome breaks at or near the centromere. In three of the four lines a marker chromosome could be identified as a rearrangement between two chromosomes. In the fourth cell line a rearranged chromosome was present in only 15% of the cells and was not studied in detail. One of the three major marker chromosomes resulted from a centromeric fusion of chromosome 4 while another appeared to be an interchange involving the centromere of chromosome 2 and possibly the telomeric region of chromosome 17.(ABSTRACT TRUNCATED AT 250 WORDS)
先前的研究表明,中国仓鼠卵巢细胞的X染色体异染色质长臂在用致癌性结晶硫化镍颗粒(crNiS)处理时会出现优先解聚(或断裂)。在本报告中,我们表明,尽管小鼠细胞中的异染色质仅限于着丝粒区域,但小鼠染色体的异染色质区域比常染色质区域更频繁地发生畸变。我们还展示了对四种细胞系的核型分析,这些细胞系源自腿部肌肉注射结晶硫化镍诱导的肿瘤,已对其进行分析以确定在转化的基因型中异染色质染色体区域是否优先发生改变。所有细胞系的共同特征是存在小染色体,它们是比19号染色体小的近端着丝粒染色体,而19号染色体通常是小鼠核型中最小的染色体。每个细胞系的大多数细胞中都存在小染色体,尽管这条额外染色体的形态在不同细胞系之间有很大差异。C带显示存在着丝粒DNA,因此这些小染色体可能是着丝粒处或其附近染色体断裂的结果。在四个细胞系中的三个中,可以将一条标记染色体鉴定为两条染色体之间的重排。在第四个细胞系中,一条重排染色体仅存在于15%的细胞中,未进行详细研究。三条主要标记染色体中的一条是由4号染色体的着丝粒融合产生的,而另一条似乎是涉及2号染色体着丝粒以及可能17号染色体端粒区域的互换。(摘要截于250字)