Brunati A M, Saggioro D, Chieco-Bianchi L, Pinna L A
FEBS Lett. 1986 Sep 29;206(1):59-63. doi: 10.1016/0014-5793(86)81340-0.
Five different types of protein kinase activities have been evaluated in cell lines from murine lymphomas induced by Abelson leukemia virus (A-MuLV), whose oncogene codes for a tyrosine protein kinase. Such activities were compared with those of normal cells and of cells transformed by Moloney leukemia virus (M-MuLV), lacking oncogene sequences in its genome. While cAMP-dependent protein kinase and casein kinase-1 do not undergo significant changes, casein kinase-2 rises in both A-MuLV and M-MuLV infected lymphocytes, becoming largely associated with the particulate fraction of transformed cells. Protein kinase-C on the other hand is unchanged in M-MuLV transformed cells but it undergoes a 2-3-fold increment in both soluble and particulate fractions of A-MuLV transformed lymphocytes, which also display high tyrosine protein kinase activity.
在由阿贝尔森白血病病毒(A-MuLV)诱导的鼠淋巴瘤细胞系中,已对五种不同类型的蛋白激酶活性进行了评估,该病毒的癌基因编码一种酪氨酸蛋白激酶。将这些活性与正常细胞以及由莫洛尼白血病病毒(M-MuLV)转化的细胞的活性进行了比较,M-MuLV在其基因组中缺乏癌基因序列。虽然依赖cAMP的蛋白激酶和酪蛋白激酶-1没有显著变化,但酪蛋白激酶-2在A-MuLV和M-MuLV感染的淋巴细胞中均升高,在很大程度上与转化细胞的颗粒部分相关。另一方面,蛋白激酶-C在M-MuLV转化的细胞中没有变化,但在A-MuLV转化的淋巴细胞的可溶性和颗粒部分中均增加了2至3倍,这些淋巴细胞也显示出高酪氨酸蛋白激酶活性。