Hue D, Dambrine G, Denesvre C, Laurent S, Wyers M, Rasschaert D
UPR 1282, INRA, Centre de Recherches de Tours, Nouzilly, France.
Arch Virol. 2006 Dec;151(12):2431-46. doi: 10.1007/s00705-006-0811-2. Epub 2006 Aug 17.
We collected paraffin-embedded myelocytomatoses induced by subgroup J avian leukosis virus (ALV-J) in French poultry from 1992 to 2000. We used nested PCR to obtain the U3 LTR and the E element sequences that encompass putative binding sites for transcription factors. We observed minor mutations in the U3 sequences that rarely affected transcription factor binding sites, thus preserving the transcriptional potential of the U3 LTR. However, we observed a large variability in the E element sequences from both field and experimental tumor samples. This variability involved genomic rearrangements and various deletions that most often occurred between two direct repeat sequences. Moreover, in seven DNA samples of the 22 field tumors analyzed, we observed two different sequences for the E element region, suggesting that proviral genomes of two different sizes may be simultaneously present in a tumor. Even though most of the E element sequences were mutated or rearranged, all myelocytomatosis samples always exhibited one E element sequence containing at least one putative C/EBP binding site that was unaffected and still potentially functional.
我们收集了1992年至2000年法国家禽中由J亚群禽白血病病毒(ALV-J)诱导产生的石蜡包埋的骨髓细胞瘤。我们使用巢式PCR获得U3长末端重复序列(LTR)和E元件序列,这些序列包含转录因子的假定结合位点。我们在U3序列中观察到微小突变,这些突变很少影响转录因子结合位点,从而保留了U3 LTR的转录潜力。然而,我们在来自田间和实验性肿瘤样本的E元件序列中观察到很大的变异性。这种变异性涉及基因组重排和各种缺失,这些缺失最常发生在两个直接重复序列之间。此外,在分析的22个田间肿瘤的7个DNA样本中,我们观察到E元件区域有两种不同的序列,这表明两种不同大小的前病毒基因组可能同时存在于一个肿瘤中。尽管大多数E元件序列发生了突变或重排,但所有骨髓细胞瘤样本始终表现出一个E元件序列,该序列包含至少一个未受影响且仍可能具有功能的假定C/EBP结合位点。