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细胞周期依赖性神经毒性靶酯酶在细胞增殖中的作用。

The role of cell cycle-dependent neuropathy target esterase in cell proliferation.

机构信息

Key Laboratory of Molecular Biology, College of Bio-Information, Chongqing University of Posts and Telecommunications, Chongqing, 400065, People's Republic of China.

出版信息

Mol Biol Rep. 2011 Jan;38(1):123-30. doi: 10.1007/s11033-010-0085-3. Epub 2010 Mar 21.

Abstract

Neuropathy target esterase (NTE) is a novel phospholipase B and plays a role in phospholipid homeostasis. Although over-expression of NTE inhibits cell division, the role of NTE in cell proliferation is still unknown. In the current study, we firstly used synchronous HeLa cells to study the expression profile of NTE during the cell cycle. NTE protein and activity are regulated during the cell cycle with highest level at G1 and lowest at G2/M phase. However, NTE mRNA levels are constant during the cell cycle. The role of NTE in cell proliferation was investigated by short hairpin RNA (shRNA) to suppress the expression of NTE. Knockdown of NTE significant down-regulated of NTE expression and reduced the glycerophosphocholine level. However, suppression of NTE did not affect phosphatidylcholine content or cell cycle progression. In addition, NTE was demonstrated to be degraded by the ubiquitin-proteasome pathway. These results suggested for the first time that NTE is a cell cycle-dependent protein, but is not essential for cell proliferation, and the ubiquitin-mediated proteolysis may be involved in the regulation of NTE during the cell cycle.

摘要

神经靶酯酶(NTE)是一种新型的磷脂酶 B,在磷脂稳态中发挥作用。尽管 NTE 的过度表达会抑制细胞分裂,但 NTE 在细胞增殖中的作用仍不清楚。在本研究中,我们首先使用同步的 HeLa 细胞研究 NTE 在细胞周期中的表达谱。NTE 蛋白和活性在细胞周期中受到调控,在 G1 期达到最高水平,在 G2/M 期达到最低水平。然而,NTE mRNA 水平在细胞周期中保持不变。通过短发夹 RNA(shRNA)抑制 NTE 的表达来研究 NTE 在细胞增殖中的作用。NTE 的敲低显著下调了 NTE 的表达,并降低了甘油磷酸胆碱水平。然而,抑制 NTE 并不影响磷脂酰胆碱含量或细胞周期进程。此外,NTE 被证明是通过泛素-蛋白酶体途径降解的。这些结果首次表明,NTE 是一种细胞周期依赖性蛋白,但对细胞增殖并非必需,泛素介导的蛋白水解可能参与了细胞周期中 NTE 的调节。

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