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异常蛋白质作为真核生物的应激信号,触发热休克基因的激活。

Abnormal proteins serve as eukaryotic stress signals and trigger the activation of heat shock genes.

作者信息

Ananthan J, Goldberg A L, Voellmy R

出版信息

Science. 1986 Apr 25;232(4749):522-4. doi: 10.1126/science.3083508.

Abstract

Heat shock protein (hsp) genes, a group of ubiquitous genes, are activated by various metabolic stresses. The suggestion that denaturation of intracellular proteins may be produced by the metabolic stresses and then signal the activation of the hsp genes was examined by co-injection of purified proteins and hsp genes into frog oocytes. Activation of hsp genes was observed if the proteins were denatured prior to injection but not if they were introduced in their native form. Furthermore, the activation of hsp genes by abnormal proteins and by heat shock appears to occur by a common mechanism. A model for the transcriptional regulation of the genes is based on competition for degradation between abnormal intracellular proteins and a labile regulatory factor.

摘要

热休克蛋白(hsp)基因是一组普遍存在的基因,可被各种代谢应激激活。通过将纯化的蛋白质和hsp基因共同注射到蛙卵母细胞中,研究了细胞内蛋白质变性可能由代谢应激产生,然后发出hsp基因激活信号这一观点。如果蛋白质在注射前变性,则可观察到hsp基因的激活,而以天然形式导入则不会激活。此外,异常蛋白质和热休克对hsp基因的激活似乎是通过共同机制发生的。该基因转录调控的模型基于异常细胞内蛋白质与不稳定调节因子之间的降解竞争。

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