Courtneidge S A, Goutebroze L, Cartwright A, Heber A, Scherneck S, Feunteun J
Differentiation Programme, European Molecular Biology Laboratory, Heidelberg, Germany.
J Virol. 1991 Jun;65(6):3301-8. doi: 10.1128/JVI.65.6.3301-3308.1991.
Hamster polyomavirus (HaPV) is associated with lymphoid and hair follicle tumors in Syrian hamsters. The early region of HaPV has the potential to encode three polypeptides (which are related to the mouse polyomavirus early proteins) and can transform fibroblasts in vitro. We identified the HaPV middle T antigen (HamT) as a 45-kDa protein. Like its murine counterpart, HamT was associated with serine/threonine phosphatase, phosphatidylinositol-3 kinase, and protein tyrosine kinase activities. However, whereas mouse middle T antigen associates predominantly with pp60c-src and pp62c-yes, HamT was associated with a different tyrosine kinase, p59fyn. The ability of HaPV to cause lymphoid tumors may therefore reside in its ability to associate with p59fyn, a potentially important tyrosine kinase in lymphocytes.
仓鼠多瘤病毒(HaPV)与叙利亚仓鼠的淋巴和毛囊肿瘤有关。HaPV的早期区域有潜力编码三种多肽(与小鼠多瘤病毒早期蛋白相关),并能在体外转化成纤维细胞。我们将HaPV中间T抗原(HamT)鉴定为一种45 kDa的蛋白质。与它的鼠类对应物一样,HamT与丝氨酸/苏氨酸磷酸酶、磷脂酰肌醇-3激酶和蛋白酪氨酸激酶活性相关。然而,小鼠中间T抗原主要与pp60c-src和pp62c-yes相关,而HamT与一种不同的酪氨酸激酶p59fyn相关。因此,HaPV导致淋巴肿瘤的能力可能在于其与p59fyn相关的能力,p59fyn是淋巴细胞中一种潜在的重要酪氨酸激酶。