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tsLA23-NRK细胞在无血清培养基中进入有丝分裂需要在G2期具备pp60v-src蛋白酪氨酸激酶活性。

tsLA23-NRK cells need pp60v-src protein-tyrosine kinase activity in G2 phase to initiate mitosis in serum-free medium.

作者信息

Durkin J P, Youdale T, Whitfield J F

机构信息

Cell Signals Group, National Research Council of Canada, Ottawa, Ontario.

出版信息

Cell Signal. 1991;3(2):93-7. doi: 10.1016/0898-6568(91)90015-m.

Abstract

Lowering the temperature from 41 to 36 degrees C stimulates quiescent tsLA23-NRK rat cells (infected with the tsLA23 mutant of the Rous sarcoma virus) in serum-free medium to resume cycling and initiate DNA replication by reactivating the tsLA23-RSV's abnormally thermolabile pp60v-src protein-tyrosine kinase. Inactivating the enzyme in these pp60v-src-stimulated cells by again raising the temperature to 41 degrees C after the cells had initiated DNA replication did not prevent the completion of DNA replication and entry into the G2 phase, but it stopped the initiation of mitosis. Adding serum at the time of the temperature increase replaced the lost pp60v-src activity and the cells were able to continue to mitosis. The G2-arrested cells at 41 degrees C were able to initiate mitosis when pp60v-src was reactivated again by lowering the temperature to 36 degrees C. These observations suggest that protein-tyrosine kinase activity is needed to initiate mitosis and that the tsLA23-NRK cell is a good model for studying the function of this kinase activity in the initiation of mitosis.

摘要

将温度从41摄氏度降至36摄氏度,可刺激无血清培养基中静止的tsLA23 - NRK大鼠细胞(感染劳氏肉瘤病毒的tsLA23突变体)恢复循环并通过重新激活tsLA23 - RSV异常热不稳定的pp60v - src蛋白酪氨酸激酶来启动DNA复制。在细胞启动DNA复制后,再次将温度升至41摄氏度使这些pp60v - src刺激的细胞中的酶失活,并未阻止DNA复制的完成和进入G2期,但阻止了有丝分裂的启动。在温度升高时添加血清可替代丧失的pp60v - src活性,细胞能够继续进行有丝分裂。当通过将温度降至36摄氏度再次激活pp60v - src时,41摄氏度下G2期阻滞的细胞能够启动有丝分裂。这些观察结果表明,启动有丝分裂需要蛋白酪氨酸激酶活性,并且tsLA23 - NRK细胞是研究该激酶活性在有丝分裂启动中的功能的良好模型。

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