首页> 美国卫生研究院文献>Journal of Virology >Integration of the BALB/c ecotropic provirus into the colony-stimulating factor-1 growth factor locus in a myc retrovirus-induced murine monocyte tumor.
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Integration of the BALB/c ecotropic provirus into the colony-stimulating factor-1 growth factor locus in a myc retrovirus-induced murine monocyte tumor.

机译:在myc逆转录病毒诱导的鼠单核细胞肿瘤中将BALB / c亲嗜性原病毒整合到集落刺激因子-1生长因子基因座中。

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摘要

The development of tumors is thought to be a multistage process that requires an unknown number of genetic or epigenetic changes in a single cell. We previously described a murine monocyte tumor which was induced by a helper-free c-myc retrovirus and which also contained a DNA rearrangement at the colony-stimulating factor-1 (CSF-1) locus. The CSF-1 gene rearrangement gave rise to high levels of growth factor production and autocrine growth, implicating this secondary event in tumorigenesis. This CSF-1 gene rearrangement was found to be the result of integration of the BALB/c ecotropic retrovirus. Restriction enzyme mapping and DNA sequence analysis demonstrated that the novel provirus is identical to the BALB/c endogenous ecotropic provirus, indicating that infection was probably not due to the creation of a recombinant virus in vivo. The proviral integration site was mapped 3 kilobases 5' of the CSF-1 promoter and in an opposite transcriptional orientation, indicating that activation of CSF-1 expression was the result of the presence of the retroviral enhancer element.
机译:肿瘤的发展被认为是一个多阶段的过程,需要在单个细胞中进行未知数量的遗传或表观遗传学改变。先前我们描述了一种由无辅助c-myc逆转录病毒诱导的鼠单核细胞肿瘤,并且该菌在集落刺激因子1(CSF-1)位点也包含DNA重排。 CSF-1基因重排导致高水平的生长因子产生和自分泌生长,这暗示了肿瘤发生中的该次要事件。发现该CSF-1基因重排是BALB / c嗜性逆转录病毒整合的结果。限制性酶切图谱和DNA序列分析表明,该新型原病毒与BALB / c内源性嗜生原病毒相同,表明感染可能不是由于体内重组病毒的产生。前病毒整合位点位于CSF-1启动子的3个碱基5'处,并处于相反的转录方向,表明CSF-1表达的激活是逆转录病毒增强子元件的存在。

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