Intercellular Communication in the Nervous System Goes Viral

被引:27
|
作者
Hantak, Michael P. [1 ]
Einstein, Jenifer [1 ]
Kearns, Rachel B. [1 ]
Shepherd, Jason D. [1 ]
机构
[1] Univ Utah, Dept Neurobiol & Anat, Salt Lake City, UT 84112 USA
基金
美国国家卫生研究院;
关键词
EXTRACELLULAR VESICLES; TRANSPOSABLE ELEMENTS; ENDOGENOUS RETROVIRUSES; SYNAPTIC PLASTICITY; PNMA FAMILY; ARC/ARG3.1; ARC; PROTEIN; GAG; NEURONS;
D O I
10.1016/j.tins.2020.12.003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Viruses and transposable elements are major drivers of evolution and make up over half the sequences in the human genome. In some cases, these elements are co-opted to perform biological functions for the host. Recent studies made the surprising observation that the neuronal gene Arc forms virus-like protein capsids that can transfer RNA between neurons to mediate a novel intercellular communication pathway. Phylogenetic analyses showed that mammalian Arc is derived from an ancient retrotransposon of the Ty3/gypsy family and contains homology to the retroviral Gag polyproteins. The Drosophila Arc homologs, which are independently derived from the same family of retrotransposons, also mediate cell-to-cell signaling of RNA at the neuromuscular junction; a striking example of convergent evolution. Here we propose an Arc ?life cycle?, based on what is known about retroviral Gag, and discuss how elucidating these biological processes may lead to novel insights into brain plasticity and memory.
引用
收藏
页码:248 / 259
页数:12
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