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Retrotransposon-induced mosaicism in the neural genome.

Gabriela O BodeaEleanor G Z McKelveyGeoffrey J Faulkner
Published in: Open biology (2019)
Over the past decade, major discoveries in retrotransposon biology have depicted the neural genome as a dynamic structure during life. In particular, the retrotransposon LINE-1 (L1) has been shown to be transcribed and mobilized in the brain. Retrotransposition in the developing brain, as well as during adult neurogenesis, provides a milieu in which neural diversity can arise. Dysregulation of retrotransposon activity may also contribute to neurological disease. Here, we review recent reports of retrotransposon activity in the brain, and discuss the temporal nature of retrotransposition and its regulation in neural cells in response to stimuli. We also put forward hypotheses regarding the significance of retrotransposons for brain development and neurological function, and consider the potential implications of this phenomenon for neuropsychiatric and neurodegenerative conditions.
Keyphrases
  • cerebral ischemia
  • resting state
  • white matter
  • functional connectivity
  • multiple sclerosis
  • subarachnoid hemorrhage
  • cell cycle arrest
  • oxidative stress
  • cell death
  • stress induced
  • endoplasmic reticulum stress