Swift R A, Boerkoel C, Ridgway A, Fujita D J, Dodgson J B, Kung H J
J Virol. 1987 Jul;61(7):2084-90. doi: 10.1128/JVI.61.7.2084-2090.1987.
Nondefective reticuloendotheliosis virus induces chicken bursal lymphoma in a manner similar to that of avian leukosis virus. The provirus integrates in the c-myc locus and uses a promoter insertion mechanism to activate c-myc expression. We cloned a provirus involved in c-myc activation from a B lymphoma. Detailed structural characterization of this clone, including sequence determination, revealed proviral insertion at 512 base pairs preceding the second c-myc exon. The provirus has a deletion of 80% of the viral genes but retains two intact long terminal repeats (LTRs). A segment of the viral env sequence is present in an inverted orientation. Elevated expression of c-myc, apparently directed by the 3' LTR, was detected. However, despite the presence of an intact 5' LTR, no viral transcripts were detected. Thus, the internal proviral rearrangement can affect 5' LTR transcription or stability of the message or both. This finding is in consonance with the view that proviral deletion plays an important role in the induction of bursal lymphomas by nonacute retroviruses.
无缺陷型网状内皮组织增生症病毒以类似于禽白血病病毒的方式诱导鸡法氏囊淋巴瘤。前病毒整合到c-myc基因座中,并利用启动子插入机制激活c-myc表达。我们从一个B淋巴瘤中克隆了一个参与c-myc激活的前病毒。对该克隆进行详细的结构表征,包括序列测定,结果显示前病毒插入在第二个c-myc外显子之前的512个碱基对处。该前病毒缺失了80%的病毒基因,但保留了两个完整的长末端重复序列(LTRs)。病毒env序列的一段以反向方向存在。检测到明显由3' LTR指导的c-myc表达升高。然而,尽管存在完整的5' LTR,但未检测到病毒转录本。因此,内部前病毒重排可影响5' LTR转录或信息的稳定性或两者。这一发现与前病毒缺失在非急性逆转录病毒诱导法氏囊淋巴瘤中起重要作用的观点一致。