Falaschi A, Biamonti G, Cobianchi F, Csordas-Toth E, Faulkner G, Giacca M, Pedacchia D, Perini G, Riva S, Tribioli C
International Centre for Genetic Engineering and Biotechnology, Trieste, Italy.
Biochim Biophys Acta. 1988 Dec 20;951(2-3):430-42. doi: 10.1016/0167-4781(88)90117-0.
We describe the purification and cloning of human DNA replicated at the onset of S phase in HL60 cells synchronized with aphidicolin. A survey of the overall structural properties of these sequences did not show any distinctive features except for an enrichment in Cot0 DNA. The two longer fragments were completely sequenced and studied in more detail. Both were shown to contain transcriptional signals associated with promoters and/or enhancers, such as the binding sites of Sp1, T antigen and nuclear factor III. In one instance, a binding site for a known cellular transcription factor (USF/MLTF) was located inside the sequence by footprinting. Accordingly, by CAT assay and Northern blot, the same sequence was shown to contain an active promoter. The significance of these findings with respect to the role of transcription in initiation of DNA replication at the origin is discussed. None of the tested fragments exhibited autonomously replicating sequence (ARS) activity in transfected cells. The problems connected with the detection of ARS activity in human cells are critically examined.
我们描述了在与阿非科林同步化的HL60细胞中,于S期起始时复制的人类DNA的纯化和克隆。对这些序列的整体结构特性进行的调查显示,除了Cot0 DNA富集外,没有任何独特特征。对两个较长的片段进行了完全测序并进行了更详细的研究。结果表明,两者均含有与启动子和/或增强子相关的转录信号,例如Sp1、T抗原和核因子III的结合位点。在一个实例中,通过足迹法在序列内部定位了一个已知细胞转录因子(USF/MLTF)的结合位点。因此,通过CAT分析和Northern印迹法,同一序列显示含有一个活性启动子。讨论了这些发现对于转录在DNA复制起始点处的作用的意义。在转染细胞中,所测试的片段均未表现出自主复制序列(ARS)活性。对与在人类细胞中检测ARS活性相关的问题进行了严格审查。