首页> 外文期刊>Cytogenetic and genome research >Dominant Expansion of a Cryptic Subclone with an Abnormal Karyotype in B Lymphoblastoid Cell Lines during Culture
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Dominant Expansion of a Cryptic Subclone with an Abnormal Karyotype in B Lymphoblastoid Cell Lines during Culture

机译:在培养期间,B淋巴母细胞系中核型异常的隐性亚克隆的显性扩增。

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Although B lymphoblastoid cell lines (B-LCLs) are thought to maintain their original genomic structures during long-term culture, there has been considerable disagreement on the actual genomic stability of these cells. This study was initiated to determine whether B-LCLs develop cell populations with abnormal genomes during culture and to search for factors important to the maintenance of the original genome. We established continuous cultures of B-LCLs for more than 6 months and analyzed the cells using array-based comparative genome hybridization (CGH) analysis, conventional karyotyping and analysis of V(D)J recombination in the immunoglobulin (Ig) gene. We found that one B-LCL acquired an extra chromosome 4 without any other genomic rearrangements at passage 16 of continuous culture. At the Ig light- and heavy-chain loci, analysis of the major cell population showed a difference between cultures at early and later passages. Another aneuploid line was detected among B-LCLs established elsewhere and deposited previously into the RIKEN Cell Bank. Our findings indicate that some of the genomic rearrangements in B-LCLs are not caused by gradual accumulation of mutations and rearrangements during the B-LCL establishment processes, but rather as a result of a change in the cell population from clones with a normal genome to clones with de novo rearrangements. It is therefore feasible to maintain B-LCLs with a normal genomic structure by cell cloning or similar treatment
机译:尽管人们认为B淋巴母细胞系(B-LCL)在长期培养过程中会保持其原始基因组结构,但在这些细胞的实际基因组稳定性上存在相当大的分歧。开始这项研究是为了确定B-LCL在培养过程中是否发育出具有异常基因组的细胞群,并寻找对维持原始基因组重要的因素。我们建立了B-LCL的连续培养超过6个月的时间,并使用基于阵列的比较基因组杂交(CGH)分析,常规核型分析和免疫球蛋白(Ig)基因中V(D)J重组的分析来分析细胞。我们发现一个B-LCL在连续培养的第16代获得了一条额外的4号染色体,而没有任何其他基因组重排。在Ig轻链和重链基因座上,对主要细胞群体的分析显示,早期传代和后期传代的培养物之间存在差异。在其他地方建立的B-LCL中检测到另一种非整倍体系,并先前沉积在RIKEN细胞库中。我们的发现表明,B-LCL中的某些基因组重排不是由B-LCL建立过程中突变和重排的逐渐积累引起的,而是由于细胞数量从具有正常基因组的克隆变为具有从头重新排列的克隆。因此,通过细胞克隆或类似的处理方法来维持具有正常基因组结构的B-LCL是可行的

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