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血清和糖皮质激素诱导激酶1通过与空间记忆形成相关的血清反应因子(SRF)和环磷腺苷效应元件结合蛋白1(CREB1)的介导来增强zif268表达。

Serum- and glucocorticoid-inducible kinase 1 enhances zif268 expression through the mediation of SRF and CREB1 associated with spatial memory formation.

作者信息

Tyan Shiaw-Wei, Tsai Ming-Chi, Lin Chien-Ling, Ma Yun-Li, Lee Eminy H Y

机构信息

Graduate Institute of Life Sciences, National Defense Medical Center, Taipei, Taiwan.

出版信息

J Neurochem. 2008 May;105(3):820-32. doi: 10.1111/j.1471-4159.2007.05186.x. Epub 2007 Dec 13.

DOI:10.1111/j.1471-4159.2007.05186.x
PMID:18088355
Abstract

Serum- and glucocorticoid-inducible kinase 1 (SGK1) has been shown to play an important role in spatial memory formation, but the molecular mechanism underlying this effect of SGK1 was not known. zif268 is an immediate early gene that is induced by water maze learning. To investigate the role of SGK1 in the regulation of zif268 expression, the dominant negative mutant of SGK1, SGK1 S422A, was infused to the hippocampal CA1 area of rats, and was found to decrease significantly the mRNA level of zif268 in both naïve animals and trained animals. SGK1 was also found to phosphorylate serum response factor (SRF) at Ser73, Ser75, and Ser99, and phosphorylate CREB1 at Ser133. Inhibition of SGK1 phosphorylation sites on SRF and CREB1 with alanine substitution significantly diminished SGK1-enhanced zif268 expression in the promoter-luciferase assay. SGK1 also phosphorylates Elk-1 and SGK1 phosphorylation of Elk-1 decreased the transcriptional activity of Elk-1. But SGK1 phosphorylation of Elk-1 did not affect SGK1-enhanced zif268 expression. Moreover, the phosphorylation of SGK1 was increased in rat CA1 area after water maze learning, accompanied by increased phosphorylation of SRF at Ser99 and increased phosphorylation of CREB1 at Ser133. All these effects were antagonized by SGK1 S422A transfection. These results together suggest that SGK1 enhances zif268 expression through the mediation of SRF and CREB1, and these signaling pathways are associated with spatial memory formation in rats.

摘要

血清和糖皮质激素诱导激酶1(SGK1)已被证明在空间记忆形成中起重要作用,但SGK1产生这种作用的分子机制尚不清楚。zif268是一种立即早期基因,可由水迷宫学习诱导产生。为了研究SGK1在zif268表达调控中的作用,将SGK1的显性负性突变体SGK1 S422A注入大鼠海马CA1区,发现其显著降低了未训练动物和训练动物中zif268的mRNA水平。还发现SGK1可在Ser73、Ser75和Ser99位点磷酸化血清反应因子(SRF),并在Ser133位点磷酸化CREB1。在启动子荧光素酶测定中,用丙氨酸取代抑制SRF和CREB1上的SGK1磷酸化位点可显著减弱SGK1增强的zif268表达。SGK1还可磷酸化Elk-1,且SGK1对Elk-1的磷酸化降低了Elk-1的转录活性。但SGK1对Elk-1的磷酸化并不影响SGK1增强的zif268表达。此外,水迷宫学习后大鼠CA1区SGK-1的磷酸化增加,同时伴有Ser99位点SRF磷酸化增加和Ser133位点CREB1磷酸化增加。所有这些效应均被SGK1 S422A转染所拮抗。这些结果共同表明,SGK1通过SRF和CREB1的介导增强zif268表达,且这些信号通路与大鼠的空间记忆形成有关。

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