Urmanova M A, Tsareva A A
Tsitologiia. 1996;38(6):630-8.
Karyotypes of eight BHK-21 (C-13) cell sublines, obtained from a variety of sources and available in the cell culture collection of our Institute, have been studied using G- and C-banding, and silver staining of chromosomes. These sublines with similar modal numbers of chromosomes (40-44) are found to vary essentially in composition of both normal chromosomes and markers. In spite of the fact that many markers are constant in several cell sublines, it was impossible to determine the marker chromosomes typical of BHK-21 (C-13) cell by analogy with those typical of HeLa cells. Our studies have shown that BHK-21 (C-13) cells exhibit nonrandom chromosomal alteration involving heterochromatic regions, particularly long arms of X- and Y-chromosomes and centromeric regions of 1, 3, 6 and X-chromosomes. Deletions of Xq, Yq and heterochromatic short arms of autosomes have also been observed. The markers more commonly consist of the material of chromosomes 1, 2, 3, 4, 5, 8, 9, 16, 17, 18, 19, X and Y.
对从多种来源获得并保存在我们研究所细胞培养库中的8个BHK - 21(C - 13)细胞亚系的核型进行了研究,采用了染色体G显带、C显带和银染技术。这些亚系的染色体众数相似(40 - 44条),但正常染色体和标记染色体的组成却有很大差异。尽管许多标记在几个细胞亚系中是恒定的,但无法通过与HeLa细胞典型标记染色体类比来确定BHK - 21(C - 13)细胞的典型标记染色体。我们的研究表明,BHK - 21(C - 13)细胞呈现出涉及异染色质区域的非随机染色体改变,特别是X和Y染色体的长臂以及1、3、6和X染色体的着丝粒区域。还观察到Xq、Yq以及常染色体异染色质短臂的缺失。这些标记更常见的是由1、2、3、4、5、8、9、16、17、18、19、X和Y染色体的物质组成。