Mautner V, Boursnell M E
Virology. 1983 Nov;131(1):1-10. doi: 10.1016/0042-6822(83)90527-5.
The nucleotide sequence of the adenovirus type 5 genome has been determined for a 620-bp region that spans the C terminus of the pVI gene and the N terminus of the hexon gene, and compared to the adenovirus type 2 DNA sequence: 25 base changes have been identified, most of which do not lead to alterations in the amino acid sequence and regulatory signals in the region. Crossover sites in three intertypic recombinants have been previously located in this region of the genome by fine restriction mapping. A sequence determination for the three recombinants, and the four ts mutants used in generating the ts+ recombinants, was carried out. The crossovers were in each case located in a small region of complete sequence homology (from 45 to 156 nucleotides long) flanked on either side by sequences derived from each parent. These structures are compatible with a reciprocal crossing over model of generalised recombination, where a recombinant joint has resolved in a region of high DNA homology. For the recombinants considered here, this region abutts onto a neighbouring region of much lower sequence homology, and it is possible that the position of the crossover is determined at least in part by the termination of branch migration at a heterologous boundary.
已确定了腺病毒5型基因组中一段620碱基对区域的核苷酸序列,该区域跨越pVI基因的C末端和六邻体基因的N末端,并与腺病毒2型的DNA序列进行了比较:已鉴定出25个碱基变化,其中大多数不会导致该区域氨基酸序列和调控信号的改变。通过精细限制酶切图谱分析,先前已将三个型间重组体中的交叉位点定位在基因组的该区域。对这三个重组体以及用于产生ts+重组体的四个温度敏感(ts)突变体进行了序列测定。在每种情况下,交叉都位于一个完全序列同源的小区域(长度为45至156个核苷酸)内,两侧分别是来自每个亲本的序列。这些结构与广义重组的相互交叉模型相符,即重组接头在高DNA同源性区域得到解决。对于此处考虑的重组体,该区域邻接一个序列同源性低得多的相邻区域,并且交叉的位置可能至少部分由异源边界处分支迁移的终止所决定。