Oxidation-Reduction Cycles of Peroxiredoxin Proteins and Nontranscriptional Aspects of Timekeeping

被引:32
作者
Hoyle, Nathaniel P. [1 ]
O'Neill, John S. [1 ]
机构
[1] MRC, Mol Biol Lab, Cambridge CB2 0QH, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
ACTIVE-SITE CYSTEINE; CIRCADIAN CLOCK; SULFINIC ACID; REDOX STATE; HYPEROXIDIZED PEROXIREDOXIN; HYDROGEN-PEROXIDE; GENE-EXPRESSION; CKI-EPSILON; KINASE; RHYTHM;
D O I
10.1021/bi5008386
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The circadian clock allows organisms to accurately predict the earths rotation and modify their behavior as a result. Genetic analyses in a variety of organisms have defined a mechanism based largely on gene expression feedback loops. However, as we delve more deeply into the mechanisms of circadian timekeeping, we are discovering that post-translational mechanisms play a key role in defining the character of the clock. We are also discovering that these modifications are inextricably linked to cellular metabolism, including redox homeostasis. A robust circadian oscillation in the redox status of the peroxiredoxins (a major class of cellular antioxidants) was recently shown to be remarkably conserved from archaea and cyanobacteria all the way to plants and animals. Furthermore, recent findings indicate that cellular redox status is coupled not only to canonical circadian gene expression pathways but also to a noncanonical transcript-independent circadian clock. The redox rhythms observed in peroxiredoxins in the absence of canonical clock mechanisms may hint at the nature of this new and hitherto unknown aspect of circadian timekeeping.
引用
收藏
页码:184 / 193
页数:10
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