New mechanisms in memory storage: piRNAs and epigenetics

被引:71
作者
Landry, Christopher D. [1 ,4 ]
Kandel, Eric R. [1 ,2 ,3 ]
Rajasethupathy, Priyamvada [1 ]
机构
[1] Columbia Univ, Dept Neurosci, New York, NY 10032 USA
[2] Howard Hughes Med Inst, Chevy Chase, MD USA
[3] Columbia Univ, Kavli Inst Brain Sci, New York, NY 10032 USA
[4] Yale Univ, New Haven, CT 06520 USA
关键词
epigenetics; DNA methylation; piRNA; small RNA; memory; DEPENDENT PROTEIN-KINASE; LONG-TERM FACILITATION; NOVO DNA METHYLATION; SMALL RNAS; SYNAPTIC PLASTICITY; BEHAVIORAL SENSITIZATION; L1; RETROTRANSPOSITION; HISTONE ACETYLATION; NEURONAL ISOFORM; TINY RNAS;
D O I
10.1016/j.tins.2013.05.004
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In recent years, a greater understanding has emerged of the role epigenetic mechanisms play in the brain, not only during development, but also in mature neurons involved in long-term memory. The identification of spatially and temporally tuned epigenetic modification of genetic loci during memory storage has revealed the remarkably input-responsive, target-specific, and long-term nature of epigenetic regulation, but the underlying mechanisms have remained elusive. New insight into these mechanisms has come from the study of small RNAs, which have emerged as regulators that can confer sequence specificity to DNA- and chromatin-modifying processes. We discuss advances in the elucidation of the epigenetic mechanisms involved in long-term memory, focusing on the role of small RNAs, and in particular piwi-interacting RNAs (piRNAs), in the epigenetic regulation underlying memory storage.
引用
收藏
页码:535 / 542
页数:8
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