Hurley T R, Amrein K E, Sefton B M
Molecular Biology and Virology Laboratory, Salk Institute, San Diego, California 92186-5800.
J Virol. 1992 Dec;66(12):7406-13. doi: 10.1128/JVI.66.12.7406-7413.1992.
Temperature-sensitive mutants of the lck tyrosine protein kinase were created by the introduction of mutations known to cause temperature sensitivity of the v-src tyrosine protein kinase of Rous sarcoma virus. p56lck activated by mutation of the regulatory site of tyrosine phosphorylation, Tyr-505, to Phe transforms fibroblasts in culture. Mutations identical to those responsible for the temperature-sensitive phenotypes of the tsNY68 and tsNY72-4 v-src mutants rendered this activated lck gene temperature sensitive for both morphological transformation and induction of growth in soft agar. The mutant proteins were incapable of cellular transformation at the nonpermissive temperature in part because of failure of the lck protein to accumulate to normal levels. Morphological transformation of fibroblasts was detectable within 24 h of a shift of cells to the permissive temperature and was essentially complete in 48 to 72 h. These mutants should prove useful for the study of the function of the lck kinase in hematopoietic cells.
通过引入已知会导致劳氏肉瘤病毒v-src酪氨酸蛋白激酶温度敏感性的突变,构建了lck酪氨酸蛋白激酶的温度敏感突变体。通过将酪氨酸磷酸化调控位点Tyr-505突变为苯丙氨酸而激活的p56lck可在培养中转化成纤维细胞。与导致tsNY68和tsNY72-4 v-src突变体温度敏感表型的突变相同的突变,使这个激活的lck基因在形态转化和软琼脂中生长诱导方面对温度敏感。突变蛋白在非允许温度下无法进行细胞转化,部分原因是lck蛋白未能积累到正常水平。在将细胞转移到允许温度后24小时内可检测到成纤维细胞的形态转化,并且在48至72小时内基本完成。这些突变体应证明对研究lck激酶在造血细胞中的功能有用。