核Hsp104在静止期间保护休眠的翻译机器
Verena Kohler1,2,3, Andreas Kohler2,4,5, Lisa Larsson Berglund6
1Department of Molecular Biosciences, The Wenner-Gren Institute, Stockholm University, 10691, Stockholm, Sweden.
Nature communications
|January 5, 2024
概括
细胞衰老会影响蛋白质质量控制. 在酵母中,Hsp104蛋白分解酶在静止期间移动到核中,以防止蛋白质聚合,并确保在营养物质可用时快速翻译重新启动.
科学领域:
- 细胞生物学 细胞生物学
- 分子生物学分子生物学
- 衰老研究研究 衰老研究
背景情况:
- 细胞蛋白质稳定,维护蛋白质稳定,随着年龄的增长而下降,导致蛋白质聚合和减少细胞活力.
- 核被认为是管理细胞质蛋白质合成机器产生的错误折叠蛋白质的关键部分.
研究的目的:
- 研究与年龄相关的代谢线索在引导蛋白分解酶Hsp104到细胞核中的作用.
- 了解Hsp104的核定位如何在酵母细胞静止期间维持核蛋白质组功能.
主要方法:
- 利用酵母作为模型生物来研究细胞衰老和蛋白质稳定.
- 研究了Hsp104的局部化,以应对代谢变化和静止期间.
- 评估了受损Hsp104核进口对细胞循环重新进入和蛋白质合成恢复的影响.
主要成果:
- 与年龄相关的代谢线索,特别是切换到呼吸代谢和减少翻译速率,将细胞质Hsp104直接导入细胞核.
- 核Hsp104与翻译启动因子eIF2相互作用,抑制静止期间的蛋白质聚合.
- 抑制Hsp104核进入静止细胞,由于蛋白质合成恢复受损,延迟了细胞周期的重新进入.
结论:
- Hsp104分解酶的细胞核分离是保护静止酵母中潜在蛋白质合成机制的重要机制.
- 这种细分确保在营养补充时及时有效地重新启动翻译,这对细胞恢复和活力至关重要.
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