Mechanisms for the epigenetic inheritance of stress response in single cells

被引:26
|
作者
Xue, Yuan [1 ,2 ]
Acar, Murat [1 ,2 ,3 ,4 ]
机构
[1] Yale Univ, Dept Mol Cellular & Dev Biol, 219 Prospect St, New Haven, CT 06511 USA
[2] Yale Univ, Syst Biol Inst, 850 West Campus Dr, West Haven, CT 06516 USA
[3] Yale Univ, Interdept Program Computat Biol & Bioinformat, 300 George St,Suite 501, New Haven, CT 06511 USA
[4] Yale Univ, Dept Phys, Prospect St, New Haven, CT 06511 USA
基金
美国国家卫生研究院;
关键词
Stress response; Msn2; Epigenetic inheritance; Single cells; Yeast; Mammalian cells; NF-KAPPA-B; KINASE-A ACTIVITY; SACCHAROMYCES-CEREVISIAE; TRANSCRIPTION FACTORS; ASYMMETRIC SEGREGATION; NUCLEAR-LOCALIZATION; DAMAGED PROTEINS; PATERNAL STRESS; YEAST; DYNAMICS;
D O I
10.1007/s00294-018-0849-1
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Cells have evolved to dynamically respond to different types of environmental and physiological stress conditions. The information about a previous stress stimulus experience by a mother cell can be passed to its descendants, allowing them to better adapt to and survive in new environments. In recent years, live-cell imaging combined with cell-lineage tracking approaches has elucidated many important principles that guide stress inheritance at the single-cell and population level. In this review, we summarize different strategies that cells can employ to pass the memory' of previous stress responses to their descendants. Among these strategies, we focus on a recent discovery of how specific features of Msn2 nucleo-cytoplasmic shuttling dynamics could be inherited across cell lineages. We also discuss how stress response can be transmitted to progenies through changes in chromatin and through partitioning of anti-stress factors and/or damaged macromolecules between mother and daughter cells during cell division. Finally, we highlight how emergent technologies will help address open questions in the field.
引用
收藏
页码:1221 / 1228
页数:8
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