Ch'ang L Y, Yang W K, Myer F E, Koh C K, Boone L R
Biology Division, Oak Ridge National Laboratory, Tennessee 37831-8077.
Virology. 1989 Feb;168(2):245-55. doi: 10.1016/0042-6822(89)90264-x.
Characteristic long terminal repeats (LTR) of approximately 700 and 750 bp were found, respectively, in the two classes (polytropic and modified polytropic) of murine leukemia virus (MuLV)-related nonecotropic nonxenotropic proviral sequences in eight individual molecular clones of RFM/Un mouse chromosomal DNA fragments. Three proviral clones, two polytropic and one modified polytropic, contained sequence deletions in the viral structural genes. Nucleotide sequence analysis revealed that 7-bp direct repeats occur at both ends of deleted sequences in intact structures and one of the repeats remains in genomes with the deletion. Specifically, the deleted sequences were a 1487-bp gag-pol sequence with ACTGCCC repeat, a 113-bp mid-pol sequence with CAGGCAA repeat, and a 1811-bp env sequence with GGTCCAG repeat. The same specific sequence deletions were found in both classes of MuLV-related proviral structures. Examination of chromosomal DNA from eight inbred laboratory mouse strains and six wild mouse species showed that a minor population of proviruses with these specific deletions were present in Mus musculus and Mus spretus, all of which contain prominent 700-bp LTR polytropic proviral structures. The 750-bp LTR modified polytropic proviral structures were phylogenetically more restricted, being equally predominant in Mus musculus domesticus mice, but minor to undetectable in Mus spretus subspecies, and absent in other wild mouse populations.
在RFM/Un小鼠染色体DNA片段的八个单独分子克隆中,在两类(多嗜性和修饰多嗜性)与鼠白血病病毒(MuLV)相关的非亲嗜性非异嗜性前病毒序列中,分别发现了约700和750 bp的特征性长末端重复序列(LTR)。三个前病毒克隆,两个多嗜性和一个修饰多嗜性,在病毒结构基因中存在序列缺失。核苷酸序列分析表明,完整结构中缺失序列的两端存在7 bp的直接重复序列,其中一个重复序列保留在有缺失的基因组中。具体而言,缺失序列为具有ACTGCCC重复序列的1487 bp gag-pol序列、具有CAGGCAA重复序列的113 bp中-pol序列和具有GGTCCAG重复序列的1811 bp env序列。在两类与MuLV相关的前病毒结构中都发现了相同的特定序列缺失。对八个近交实验室小鼠品系和六个野生小鼠物种的染色体DNA进行检测,结果显示小家鼠和西班牙小鼠中存在少量具有这些特定缺失的前病毒群体,它们都含有显著的700 bp LTR多嗜性前病毒结构。750 bp LTR修饰多嗜性前病毒结构在系统发育上受到更多限制,在小家鼠中同样占主导地位,但在西班牙小鼠亚种中较少至无法检测到,在其他野生小鼠群体中则不存在。