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HeLa细胞中钠钾激活ATP酶的稳定基因扩增及过表达

Stable gene amplification and overexpression of sodium- and potassium-activated ATPase in HeLa cells.

作者信息

Pauw P G, Johnson M D, Moore P, Morgan M, Fineman R M, Kalka T, Ash J F

出版信息

Mol Cell Biol. 1986 Apr;6(4):1164-71. doi: 10.1128/mcb.6.4.1164-1171.1986.

Abstract

Cell lines stably resistant to ouabain were isolated from an unstably resistant HeLa line after growth in nonselective medium. Stable resistant lines bound ouabain at levels 10-fold higher than did HeLa cells and at similar levels to those bound by the unstable C+ line previously described (J. F. Ash, R. M. Fineman, T. Kalka, M. Morgan, and B. Wire, J. Cell Biol. 99: 971-983). Expression and synthesis of the Na+, K+ -ATPase alpha chain showed a similar amplification over that for HeLa cells by Western blots and [35S]methionine pulse-labeling. In addition, a glycoprotein labeled with [3H]fucose and comigrating with the Na+, K+ -ATPase beta chain was eight- to ninefold amplified in stably resistant lines. Dot blots with a cDNA clone specific for Na+, K+ -ATPase alpha chain gene sequences confirmed the amplification of this gene. Karyotyping suggested that the amplification is associated with an expanded, abnormal banded region on the long (q) arm of one chromosome 17.

摘要

在非选择性培养基中生长后,从不稳定耐药的HeLa细胞系中分离出对哇巴因稳定耐药的细胞系。稳定耐药细胞系结合哇巴因的水平比HeLa细胞高10倍,与先前描述的不稳定C +细胞系结合的水平相似(J.F. Ash、R.M. Fineman、T. Kalka、M. Morgan和B. Wire,《细胞生物学杂志》99: 971 - 983)。通过蛋白质免疫印迹法和[35S]甲硫氨酸脉冲标记法,Na +, K + -ATP酶α链的表达和合成相对于HeLa细胞显示出类似的扩增。此外,在稳定耐药细胞系中,一种用[3H]岩藻糖标记且与Na +, K + -ATP酶β链共迁移的糖蛋白扩增了8至9倍。用针对Na +, K + -ATP酶α链基因序列的cDNA克隆进行斑点印迹证实了该基因的扩增。核型分析表明,扩增与17号染色体一条长臂(q)上一个扩展的异常带区有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7ff/367628/38736ada7e2f/molcellb00088-0209-a.jpg

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