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Cyclin F, Neurodegeneration, and the Pathogenesis of ALS/FTD.

Stephanie L RaynerAlison HoganJennilee M DavidsonFlora ChengLuan LuuMarco MorschIan BlairRoger ChungAlbert Lee
Published in: The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry (2022)
Amyotrophic lateral sclerosis (ALS) is the most common form of motor neuron disease and is characterized by the degeneration of upper and lower motor neurons of the brain and spinal cord. ALS is also linked clinically, genetically, and pathologically to a form of dementia known as frontotemporal dementia (FTD). Identifying gene mutations that cause ALS/FTD has provided valuable insight into the disease process. Several ALS/FTD-causing mutations occur within proteins with roles in protein clearance systems. This includes ALS/FTD mutations in CCNF , which encodes the protein cyclin F: a component of a multiprotein E3 ubiquitin ligase that mediates the ubiquitylation of substrates for their timely degradation. In this review, we provide an update on the link between ALS/FTD CCNF mutations and neurodegeneration.
Keyphrases
  • amyotrophic lateral sclerosis
  • spinal cord
  • cell cycle
  • multiple sclerosis
  • cognitive impairment
  • cell proliferation
  • white matter
  • binding protein