Convergence of the SUMO and MAPK pathways on the ETS-domain transcription factor Elk-1.

Shen-Hsi Yang, Andrew D Sharrocks
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引用次数: 49

Abstract

The ETS-domain transcription factor Elk-1 is regulated by phosphorylation in response to activation of the MAPK (mitogen-activated protein kinase) pathways. This phosphorylation triggers a series of molecular events that convert Elk-1 from a transcriptionally silent state into a highly active state and then back to a basal level. At the same time, activation of the ERK (extracellular-signal-regulated kinase) MAPK pathway leads to loss of modification of Elk-1 by SUMO (small ubiquitin-related modifier). As SUMO imparts repressive properties on Elk-1, ERK-mediated SUMO loss leads to de-repression at the same time as the ERK pathway promotes activation of Elk-1. Thus a two-step mechanism is employed to convert Elk-1 into its fully activated state. Here, the molecular events underlying these changes in Elk-1 status, and the role of PIASxalpha [protein inhibitor of activated STAT (signal transducer and activator of transcription) xalpha] as a co-activator that facilitates this process, are discussed.

ets结构域转录因子Elk-1上SUMO和MAPK通路的收敛。
ets结构域转录因子Elk-1受MAPK(丝裂原活化蛋白激酶)通路激活的磷酸化调控。这种磷酸化引发了一系列分子事件,将Elk-1从转录沉默状态转化为高度活跃状态,然后回到基础水平。同时,ERK(细胞外信号调节激酶)MAPK通路的激活导致Elk-1被SUMO(小泛素相关修饰物)修饰的丧失。由于SUMO赋予Elk-1抑制特性,ERK介导的SUMO缺失导致去抑制,同时ERK通路促进Elk-1的激活。因此,采用两步机制将Elk-1转化为完全激活状态。本文讨论了Elk-1状态变化背后的分子事件,以及PIASxalpha[活化STAT(信号换能器和转录激活因子)xalpha的蛋白抑制剂]作为促进这一过程的共激活因子的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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