Protein-Based Inheritance: Epigenetics beyond the Chromosome

被引:139
作者
Harvey, Zachary H. [1 ]
Chen, Yiwen [1 ]
Jarosz, Daniel F. [1 ,2 ]
机构
[1] Stanford Univ, Sch Med, Dept Chem & Syst Biol, 269 Campus Dr, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Dev Biol, 269 Campus Dr, Stanford, CA 94305 USA
关键词
INTRINSICALLY DISORDERED PROTEINS; DE-NOVO APPEARANCE; PRION-LIKE FACTOR; SACCHAROMYCES-CEREVISIAE; PHASE-SEPARATION; PSI+ PRION; YEAST; SUP35; GENE; TRANSMISSION;
D O I
10.1016/j.molcel.2017.10.030
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
Epigenetics refers to changes in phenotype that are not rooted in DNA sequence. This phenomenon has largely been studied in the context of chromatin modification. Yet many epigenetic traits are instead linked to self-perpetuating changes in the individual or collective activity of proteins. Most such proteins are prions (e. g., [PSI+], [URE3], [SWI+], [MOT3(+)], [MPH1(+)], [LSB+], and [GAR(+)]), which have the capacity to adopt at least one conformation that self-templates over long biological timescales. This allows them to serve as proteinbased epigenetic elements that are readily broadcast through mitosis and meiosis. In some circumstances, self-templating can fuel disease, but it also permits access to multiple activity states from the same polypeptide and transmission of that information across generations. Ensuing phenotypic changes allow genetically identical cells to express diverse and frequently adaptive phenotypes. Although long thought to be rare, protein- based epigenetic inheritance has now been uncovered in all domains of life.
引用
收藏
页码:195 / 202
页数:8
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