Adams S E, Rathjen P D, Stanway C A, Fulton S M, Malim M H, Wilson W, Ogden J, King L, Kingsman S M, Kingsman A J
Department of Biochemistry, University of Oxford, United Kingdom.
Mol Cell Biol. 1988 Aug;8(8):2989-98. doi: 10.1128/mcb.8.8.2989-2998.1988.
The complete nucleotide sequence of a mouse retro-element is presented. The cloned element is composed of 4,834 base pairs (bp) with long terminal repeats of 568 bp separated by an internal region of 3,698 bp. The element did not appear to have any open reading frames that would be capable of encoding the functional proteins that are normally produced by retro-elements. However, some regions of the genome showed some homology to retroviral gag and pol open reading frames. There was no region in VL30 corresponding to a retroviral env gene. This implies that VL30 is related to retrotransposons rather than to retroviruses. The sequence also contained regions that were homologous to known reverse transcriptase priming sites and viral packaging sites. These observations, combined with the known transcriptional capacity of the VL30 promoter, suggest that VL30 relies on protein functions of other retro-elements, such as murine leukemia virus, while maintaining highly conserved cis-active promoter, packaging, and priming sites necessary for its replication and cell-to-cell transmission.
本文展示了一种小鼠逆转录元件的完整核苷酸序列。克隆得到的元件由4834个碱基对(bp)组成,其长末端重复序列为568 bp,中间间隔着一个3698 bp的内部区域。该元件似乎没有任何能够编码逆转录元件通常产生的功能蛋白的开放阅读框。然而,基因组的一些区域与逆转录病毒的gag和pol开放阅读框存在一定的同源性。VL30中没有与逆转录病毒env基因相对应的区域。这意味着VL30与逆转座子相关,而非逆转录病毒。该序列还包含与已知逆转录酶引物位点和病毒包装位点同源的区域。这些观察结果,结合VL30启动子已知的转录能力,表明VL30依赖于其他逆转录元件(如小鼠白血病病毒)的蛋白质功能,同时维持其复制和细胞间传播所必需的高度保守的顺式活性启动子、包装和引物位点。