James Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky, United States of America.
Department of Medicine, University of Louisville, Louisville, Kentucky, United States of America.
PLoS One. 2018 Apr 9;13(4):e0195625. doi: 10.1371/journal.pone.0195625. eCollection 2018.
The Florida manatee (Trichechus manatus latirotris) is a threatened aquatic mammal in United States coastal waters. Over the past decade, the appearance of papillomavirus-induced lesions and viral papillomatosis in manatees has been a concern for those involved in the management and rehabilitation of this species. To date, three manatee papillomaviruses (TmPVs) have been identified in Florida manatees, one forming cutaneous lesions (TmPV1) and two forming genital lesions (TmPV3 and TmPV4). We identified DNA sequences with the potential to form G-quadruplex structures (G4) across the three genomes. G4 were located on both DNA strands and across coding and non-coding regions on all TmPVs, offering multiple targets for viral control. Although G4 have been identified in several viral genomes, including human PVs, most research has focused on canonical structures comprised of three G-tetrads. In contrast, the vast majority of sequences we identified would allow the formation of non-canonical structures with only two G-tetrads. Our biophysical analysis confirmed the formation of G4 with parallel topology in three such sequences from the E2 region. Two of the structures appear comprised of multiple stacked two G-tetrad structures, perhaps serving to increase structural stability. Computational analysis demonstrated enrichment of G4 sequences on all TmPVs on the reverse strand in the E2/E4 region and on both strands in the L2 region. Several G4 sequences occurred at similar regional locations on all PVs, most notably on the reverse strand in the E2 region. In other cases, G4 were identified at similar regional locations only on PVs forming genital lesions. On all TmPVs, G4 sequences were located in the non-coding region near putative E2 binding sites. Together, these findings suggest that G4 are possible regulatory elements in TmPVs.
佛罗里达海牛(Trichechus manatus latirotris)是美国沿海水域受到威胁的水生哺乳动物。在过去的十年中,海牛中乳头瘤病毒诱导的病变和病毒性乳头状瘤病的出现一直是参与该物种管理和康复的人们关注的问题。迄今为止,已在佛罗里达海牛中鉴定出三种海牛乳头瘤病毒(TmPV),一种形成皮肤病变(TmPV1),两种形成生殖器病变(TmPV3 和 TmPV4)。我们鉴定了在三个基因组中具有形成 G-四链体结构(G4)潜力的 DNA 序列。G4 位于两条 DNA 链上,跨越所有 TmPV 的编码和非编码区域,为病毒控制提供了多个靶标。尽管已经在包括人类乳头瘤病毒在内的几种病毒基因组中鉴定出 G4,但大多数研究都集中在由三个 G-四联体组成的典型结构上。相比之下,我们鉴定的大多数序列只允许形成具有两个 G-四联体的非典型结构。我们的生物物理分析证实了来自 E2 区域的三个序列中平行拓扑结构的 G4 的形成。这两个结构似乎由多个堆叠的两个 G-四联体结构组成,可能有助于提高结构稳定性。计算分析表明,在 E2/E4 区域的反向链上以及在 L2 区域的两条链上,所有 TmPV 上的 G4 序列都丰富。在所有 PV 上,几个 G4 序列出现在相似的区域位置,特别是在 E2 区域的反向链上。在其他情况下,只有在形成生殖器病变的 PV 上才能在相似的区域位置识别出 G4。在所有 TmPV 上,G4 序列位于非编码区,靠近推定的 E2 结合位点。综上所述,这些发现表明 G4 可能是 TmPV 的调节元件。