Kumar S, Giacca M, Norio P, Biamonti G, Riva S, Falaschi A
International Centre for Genetic Engineering and Biotechnology, Trieste, Italy.
Nucleic Acids Res. 1996 Sep 1;24(17):3289-94. doi: 10.1093/nar/24.17.3289.
In the past, a highly sensitive and efficient method was developed to map DNA replication origins in human cells, based on quantitative PCR performed on nascent DNA samples. This method allowed the identification of a replication origin in the myeloid HL-60 cell line, located on chromosome 19 within an approximately 500 bp segment near the lamin B2 gene [Giacca et al. (1994) Proc. Natl. Acad. Sci. USA, 91, 7119]. The same procedure has now been further simplified and extended to a variety of other exponentially growing human cells of different histological derivation (three neural, one connectival and one epithelial), with a nearly diploid chromosomal content. In all the six cell lines tested, the origin activity within the lamin B2 gene domain was localized to the same region. Furthermore, the lamin B2 origin was also found to be active in stimulated, but not in quiescent, peripheral blood lymphocytes.
过去,基于对新生DNA样本进行的定量PCR,开发了一种高度灵敏且高效的方法来绘制人类细胞中的DNA复制起点图谱。该方法使得在髓系HL-60细胞系中鉴定出一个复制起点,它位于19号染色体上靠近层粘连蛋白B2基因的一个约500 bp片段内[贾卡等人(1994年),《美国国家科学院院刊》,91, 7119]。现在,相同的程序已进一步简化,并扩展到了多种来自不同组织学来源(三种神经组织、一种结缔组织和一种上皮组织)且染色体含量近乎二倍体的其他指数生长的人类细胞。在所有测试的六种细胞系中,层粘连蛋白B2基因区域内的起点活性定位于同一区域。此外,还发现层粘连蛋白B2起点在受刺激的外周血淋巴细胞中具有活性,但在静止的外周血淋巴细胞中无活性。