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一种与Dicer相关的解旋酶可对抗ASI神经元中SKN-1激活所导致的与衰老相关的病理变化。

A dicer-related helicase opposes the age-related pathology from SKN-1 activation in ASI neurons.

作者信息

Turner Chris D, Stuhr Nicole L, Ramos Carmen M, Van Camp Bennett T, Curran Sean P

出版信息

bioRxiv. 2023 Oct 2:2023.10.01.560409. doi: 10.1101/2023.10.01.560409.

Abstract

UNLABELLED

Coordination of cellular responses to stress are essential for health across the lifespan. The transcription factor SKN-1 is an essential homeostat that mediates survival in stress-inducing environments and cellular dysfunction, but constitutive activation of SKN-1 drives premature aging thus revealing the importance of turning off cytoprotective pathways. Here we identify how SKN-1 activation in two ciliated ASI neurons in results in an increase in organismal transcriptional capacity that drives pleiotropic outcomes in peripheral tissues. An increase in the expression of established SKN-1 stress response and lipid metabolism gene classes of RNA in the ASI neurons, in addition to the increased expression of several classes of non-coding RNA, define a molecular signature of animals with constitutive SKN-1 activation and diminished healthspan. We reveal neddylation as a novel regulator of the SKN-1 homeostat that mediates SKN-1 abundance within intestinal cells. Moreover, RNAi-independent activity of the dicer-related DExD/H-box helicase, , in the intestine, can oppose the e2ffects of aberrant SKN-1 transcriptional activation and delays age-dependent decline in health. Taken together, our results uncover a cell non-autonomous circuit to maintain organism-level homeostasis in response to excessive SKN-1 transcriptional activity in the sensory nervous system.

SIGNIFICANCE STATEMENT

Unlike activation, an understudied fundamental question across biological systems is how to deactivate a pathway, process, or enzyme after it has been turned on. The irony that the activation of a transcription factor that is meant to be protective can diminish health was first documented by us at the organismal level over a decade ago, but it has long been appreciated that chronic activation of the human ortholog of SKN-1, NRF2, could lead to chemo- and radiation resistance in cancer cells. A colloquial analogy to this biological idea is a sink faucet that has an on valve without a mechanism to shut the water off, which will cause the sink to overflow. Here, we define this off valve.

摘要

未标记

细胞对应激反应的协调对于整个生命周期的健康至关重要。转录因子SKN-1是一种重要的稳态调节因子,介导在应激诱导环境中的存活和细胞功能障碍,但SKN-1的组成性激活会导致早衰,从而揭示了关闭细胞保护途径的重要性。在这里,我们确定了秀丽隐杆线虫中两个具纤毛的ASI神经元中的SKN-1激活如何导致机体转录能力增加,从而在外周组织中驱动多效性结果。ASI神经元中既定的SKN-1应激反应和脂质代谢基因类别的RNA表达增加,以及几类非编码RNA的表达增加,定义了具有组成性SKN-1激活和健康寿命缩短的动物的分子特征。我们揭示了NEDDylation是SKN-1稳态的一种新型调节因子,可介导肠道细胞内SKN-1的丰度。此外,肠道中与dicer相关的DExD/H盒解旋酶DRH-1的RNAi非依赖性活性可以对抗异常SKN-1转录激活的影响,并延缓年龄依赖性的健康衰退。综上所述,我们的结果揭示了一个细胞非自主性回路,以响应感觉神经系统中过量的SKN-1转录活性来维持机体水平的稳态。

意义声明

与激活不同,生物系统中一个研究较少的基本问题是,在一个途径、过程或酶被开启后如何将其关闭。十多年前,我们首次在机体水平记录了一个具有保护作用的转录因子的激活会损害健康这一具有讽刺意味的现象,但长期以来人们一直认识到,SKN-1的人类直系同源物NRF2的慢性激活可能导致癌细胞产生化学抗性和辐射抗性。对此生物学观点的一个通俗比喻是,一个水槽水龙头只有打开阀门的机制,而没有关闭水流的机制,这将导致水槽溢出。在这里,我们定义了这个关闭阀门。

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