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FISH studies on the telomeric regions of the T-cell acute lymphoblastic leukemia cell line CCRF-CEM

机译:FISH对T细胞急性淋巴细胞白血病细胞CCRF-CEM端粒区域的研究

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So far, the problem of an influence of translocations on the telomeres of the involved chromosomes has not been addressed yet in human cells. Therefore, the telomeres of a karyotypically rather well characterized T-cell acute lymphoblastic leukemia (T-ALL) cell line (CCRF-CEM) with several marker chromosomes were examined using peptide nucleic acid (PNA) telomere FISH probes to compare the telomere length of these markers with that of the chromosome arms of their origin. In addition, chromosome libraries, centromeric probes, and subtelomeric DNA probes were used to further define the marker chromosomes. Two markers could be newly defined and a concise karyotype of the cell line could be obtained by these detailed examinations: 42-47,X,-X,del(5) (q35?),t(5; 15)(q14;q 13.2),t(8; 9)(p11;p24),del(9)(:p 13 -> qter)/ inv(9)(pter -> p12::q21 -> q21 -> qter),+ 13,+20,+der(22)(p+ [HSR?])[cp). The relative telomere length of all chromosomes showed considerable interchromosomal, intercellular, and inter-passage variation. However, it could be shown, that in four different passages of the examined cell line the observed differences between relative telomere lengths of the markers and the chromosomes of their origin, with two exceptions (short arms of del/inv9 and der22), were not significant. On the other hand, because of its mentioned variability, telomere length alone is not sufficient to reliably define the derivation of markers.Copyright (c) 2005 S. KargerAG, Basel.
机译:迄今为止,在人类细胞中尚未解决易位对所涉及染色体的端粒的影响的问题。因此,使用肽核酸(PNA)端粒FISH探针检查了具有几个标记染色体的核型典型的特征良好的T细胞急性淋巴细胞白血病(T-ALL)细胞系(CCRF-CEM)的端粒,以比较这些标记与其起源的染色体臂的标记相同。此外,染色体文库,着丝粒探针和亚端粒DNA探针用于进一步定义标记染色体。通过这些详细的检查,可以重新定义两个标记,并可以得出细胞系的简洁核型:42-47,X,-X,del(5)(q35?),t(5; 15)(q14; q 13.2),t(8; 9)(p11; p24),del(9)(:p 13-> qter)/ inv(9)(pter-> p12 :: q21-> q21-> qter),+ 13 ,+ 20,+ der(22)(p + [HSR?])[cp)。所有染色体的相对端粒长度显示出相当大的染色体间,细胞间和通道间变异。然而,可以证明,在所检查的细胞系的四个不同传代中,标记的相对端粒长度与其起源的染色体之间观察到的差异(两个例外(del / inv9和der22的短臂)除外)重大。另一方面,由于其提到的可变性,仅端粒长度不足以可靠地确定标记的衍生。(c)2005 S. KargerAG,巴塞尔。

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