Bösze Z, Thiesen H J, Charnay P
EMBO J. 1986 Jul;5(7):1615-23. doi: 10.1002/j.1460-2075.1986.tb04404.x.
We investigated the ability of the U3 region of the long terminal repeats (LTR) of the Friend murine leukemia virus (Fr-MuLV) and Moloney murine leukemia virus (Mo-MuLV) to promote transcription in a variety of human cell lines. Our analysis reveals the presence of a transcriptional enhancer with specificity for erythroid cells in the U3 region of the Fr-MuLV. This constitutes the first example of an enhancer with such a property. Analysis of the Mo-MuLV enhancer suggests that it is active at least in erythroid and lymphoid cells and has thus a less restricted specificity than the Fr-MuLV enhancer. The different tissue specificities of the two enhancers correlate with the different tissue selectivities and pathogenic properties of the two viruses.
我们研究了弗氏小鼠白血病病毒(Fr-MuLV)和莫洛尼小鼠白血病病毒(Mo-MuLV)长末端重复序列(LTR)的U3区域在多种人类细胞系中促进转录的能力。我们的分析揭示,在Fr-MuLV的U3区域存在一种对红系细胞具有特异性的转录增强子。这是具有这种特性的增强子的首个实例。对Mo-MuLV增强子的分析表明,它至少在红系和淋巴系细胞中具有活性,因此与Fr-MuLV增强子相比,其特异性限制较少。两种增强子不同的组织特异性与两种病毒不同的组织选择性和致病特性相关。