Olsen A S, McBride O W, Moore D E
Laboratory of Biochemistry, National Cancer Institute, Bethesda, Maryland 20205.
Mol Cell Biol. 1981 May;1(5):439-48. doi: 10.1128/mcb.1.5.439-448.1981.
Labeled probes of unique-sequence human X chromosomal deoxyribonucleic acid, prepared by two different procedures, were used to measure the amount of human X chromosomal deoxyribonucleic acid in 12 mouse cell lines expressing human hypoxanthine phosphoribosyltransferase after chromosome-mediated gene transfer. The amount of X chromosomal deoxyribonucleic acid detected by this procedure ranged from undetectable levels in the three stable transformants and some unstable transformants examined to about 20% of the human X chromosome in two unstable transformants. Reassociation kinetics of the X chromosomal probe with deoxyribonucleic acid from the two unstable transformants containing 15 to 20% of the human X chromosome indicate that a single copy of these sequences is present. In one of these lines, the X chromosomal sequences exist as multiple fragments which were not concordantly segregated when the cells were selected for loss of hprt.
通过两种不同程序制备的独特序列人类X染色体脱氧核糖核酸的标记探针,用于测量12个在染色体介导的基因转移后表达人类次黄嘌呤磷酸核糖转移酶的小鼠细胞系中人类X染色体脱氧核糖核酸的量。通过该程序检测到的X染色体脱氧核糖核酸的量,在所检测的三个稳定转化体和一些不稳定转化体中为不可检测水平,在两个不稳定转化体中约为人类X染色体的20%。X染色体探针与来自含有15%至20%人类X染色体的两个不稳定转化体的脱氧核糖核酸的重缔合动力学表明,这些序列存在单拷贝。在其中一个细胞系中,X染色体序列以多个片段形式存在,当细胞因hprt缺失而被选择时,这些片段并未一致分离。