Schellner J, Stüber K, Doerfler W
Biochim Biophys Acta. 1986 Jun 20;867(3):114-23. doi: 10.1016/0167-4781(86)90071-0.
In previous work we have cloned and determined the nucleotide sequence of sites of linkage between mammalian cell DNA and foreign (viral) DNA. These investigations have been performed to study details of the mechanism of recombination in mammalian cells. Cloned lines of adenovirus-transformed cells have been used in the analyses because they constituted cell populations in which the foreign DNA had been fixed at certain sites in the cellular genomes. In the present investigation, these nucleotide sequences at sites of linkage have been subjected to computer-aided analyses. A number of sequence motifs have been determined; sequence features common to all junction sites have not been discernible. In some instances, patch homologies have been detected. At several sites of junction, the cellular DNA sequences seem to be transcriptionally active, even in cells that do not carry foreign DNA. Transcriptional activity may be a necessary but perhaps not sufficient precondition for recombination of mammalian DNA sequences with foreign DNA.
在先前的工作中,我们克隆并测定了哺乳动物细胞DNA与外源(病毒)DNA之间的连接位点的核苷酸序列。进行这些研究是为了探究哺乳动物细胞中重组机制的细节。分析中使用了腺病毒转化细胞的克隆系,因为它们构成了细胞群体,其中外源DNA已固定在细胞基因组的某些位点。在本研究中,对连接位点处的这些核苷酸序列进行了计算机辅助分析。已确定了许多序列基序;尚未发现所有连接位点共有的序列特征。在某些情况下,检测到了片段同源性。在几个连接位点处,细胞DNA序列似乎具有转录活性,即使在不携带外源DNA的细胞中也是如此。转录活性可能是哺乳动物DNA序列与外源DNA重组的必要但可能不充分的前提条件。