Lee E J, Kaminchik J, Hankins W D
J Virol. 1984 Jul;51(1):247-50. doi: 10.1128/JVI.51.1.247-250.1984.
Using a DNA probe prepared from cloned env gene sequences of Friend spleen focus-forming viruses, we detected the differential expression of multiple RNA species in uninfected DBA/2 fibroblasts and in various tissues from adult DBA/2 and NZB mice. The size of the major RNA species detected was estimated to be 24S . The 24S RNA species was enriched in polyadenylate-selected preparations and thus may represent a message for endogenous viral envelope glycoproteins. The viral origin of the 24S RNA was further characterized by its hybridization to DNA probes containing the long terminal repeats of Harvey murine sarcoma virus, mouse mammary tumor virus, or the U3 region of an endogenous xenotropic virus. Although the env-related 24S RNA failed to react with either Harvey murine sarcoma virus or mouse mammary tumor virus long terminal repeat probes, it hybridized well with the xenotropic virus long terminal repeat probe. Therefore, it is likely that the RNA detected with the Friend spleen focus-forming virus env probe reflects transcription of xenotropic envelope sequences in uninfected tissues. Our finding that the level of 24S RNA varied in different organs indicated some tissue specificity in the expression of these xenotropic-like env proteins.
利用从弗氏脾脏灶形成病毒的克隆env基因序列制备的DNA探针,我们检测了未感染的DBA/2成纤维细胞以及成年DBA/2和NZB小鼠的各种组织中多种RNA种类的差异表达。检测到的主要RNA种类的大小估计为24S。24S RNA种类在聚腺苷酸选择的制剂中富集,因此可能代表内源性病毒包膜糖蛋白的信使。通过与含有哈维鼠肉瘤病毒、小鼠乳腺肿瘤病毒的长末端重复序列或内源性嗜异性病毒的U3区域的DNA探针杂交,进一步表征了24S RNA的病毒起源。尽管与env相关的24S RNA未能与哈维鼠肉瘤病毒或小鼠乳腺肿瘤病毒长末端重复探针发生反应,但它与嗜异性病毒长末端重复探针杂交良好。因此,用弗氏脾脏灶形成病毒env探针检测到的RNA可能反映了未感染组织中嗜异性包膜序列的转录。我们发现24S RNA的水平在不同器官中有所变化,这表明这些嗜异性样env蛋白的表达具有一定的组织特异性。