Yoshimura F K, Tupper J, Diem K
Department of Biological Structure, University of Washington, Seattle 98195.
J Virol. 1989 Nov;63(11):4945-8. doi: 10.1128/JVI.63.11.4945-4948.1989.
Long terminal repeat (LTR) sequences of murine leukemia viruses (MLVs) have been demonstrated to be mainly responsible for the pathogenic differences in these retroviruses. A region of the LTR which is downstream of the enhancer elements has been shown to contribute both to enhancer activity as well as to disease specificity of MLVs. We have identified protein-DNA complexes generated by this region of a lymphomagenic MLV (MCF13) and one which is nonpathogenic (Akv). One protein-DNA complex we have observed for this region is unique to MCF13 DNA sequences. Detection of protein involved in this unique MCF13 complex in different cell lines revealed that it was ubiquitous.
小鼠白血病病毒(MLV)的长末端重复序列(LTR)已被证明是这些逆转录病毒致病性差异的主要原因。LTR中增强子元件下游的一个区域已被证明既有助于增强子活性,也有助于MLV的疾病特异性。我们已经鉴定出由致淋巴瘤性MLV(MCF13)的这一区域和一种非致病性MLV(Akv)产生的蛋白质-DNA复合物。我们在该区域观察到的一种蛋白质-DNA复合物是MCF13 DNA序列所特有的。在不同细胞系中检测参与这种独特的MCF13复合物的蛋白质,发现它普遍存在。