Laprevotte I
Laboratoire d'Hématologie Expérimentale (CNRS), Centre Hayem, Hôpital Saint-Louis, Paris, France.
J Mol Evol. 1989 Aug;29(2):135-48. doi: 10.1007/BF02100112.
The present study is a detailed computer-assisted analysis of the feline leukemia virus gag gene nucleotide sequence together with its flanking sequences (ST-FeLV GAG) that is compared with the aligned sectors of the Moloney strain of murine leukemia virus (Mo-MuLV GAG) and of three strains of feline sarcoma virus. It shows that perfectly matched repeated oligomers up to 13 nucleotides long are overrepresented and scattered throughout both ST-FeLV GAG and Mo-MuLV GAG, in noncoding and coding sectors, with no stringent correlation to codon usage in ST-FeLV gPr80gag. Many repeated oligomers share a core consensus that is intriguingly part of the inverted repeat at the termini of the long terminal repeat. Local scrambled repetitions of nucleotide subsequences have been found; they suggest a model of molecular evolution by slippage-like mechanisms. Thus, viral genomes could be subject to the same evolutionary mechanisms that are now known to be operating extensively in eukaryotic genomes. The data are discussed in light of putative patterns of molecular evolution.
本研究是对猫白血病病毒gag基因核苷酸序列及其侧翼序列(ST-FeLV GAG)进行的详细计算机辅助分析,该序列与莫洛尼鼠白血病病毒(Mo-MuLV GAG)以及三种猫肉瘤病毒株的比对区段进行了比较。研究表明,长达13个核苷酸的完全匹配重复寡聚物在ST-FeLV GAG和Mo-MuLV GAG的非编码区和编码区均过度存在且分散分布,与ST-FeLV gPr80gag中的密码子使用没有严格相关性。许多重复寡聚物共享一个核心共有序列,该序列有趣地是长末端重复序列末端反向重复序列的一部分。已发现核苷酸子序列的局部混乱重复;它们提示了一种类似滑动机制的分子进化模型。因此,病毒基因组可能受到目前已知在真核基因组中广泛运作的相同进化机制的影响。根据推测的分子进化模式对数据进行了讨论。