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Deletion of Topoisomerase 1 in excitatory neurons causes genomic instability and early onset neurodegeneration.

Giulia Fragola | Angela M Mabb | Bonnie Taylor-Blake | Jesse K Niehaus | William D Chronister | Hanqian Mao | Jeremy M Simon | Hong Yuan | Zibo Li | Michael J McConnell | Mark J Zylka
Nature communications | 2020

Topoisomerase 1 (TOP1) relieves torsional stress in DNA during transcription and facilitates the expression of long (>100 kb) genes, many of which are important for neuronal functions. To evaluate how loss of Top1 affected neurons in vivo, we conditionally deleted (cKO) Top1 in postmitotic excitatory neurons in the mouse cerebral cortex and hippocampus. Top1 cKO neurons develop properly, but then show biased transcriptional downregulation of long genes, signs of DNA damage, neuroinflammation, increased poly(ADP-ribose) polymerase-1 (PARP1) activity, single-cell somatic mutations, and ultimately degeneration. Supplementation of nicotinamide adenine dinucleotide (NAD+) with nicotinamide riboside partially blocked neurodegeneration, and increased the lifespan of Top1 cKO mice by 30%. A reduction of p53 also partially rescued cortical neuron loss. While neurodegeneration was partially rescued, behavioral decline was not prevented. These data indicate that reducing neuronal loss is not sufficient to limit behavioral decline when TOP1 function is disrupted.

Pubmed ID: 32327659

Associated grants

  • Agency: NIEHS NIH HHS, United States
    Id: P30 ES010126
  • Agency: NIEHS NIH HHS, United States
    Id: R35 ES028366
  • Agency: NINDS NIH HHS, United States
    Id: P30 NS045892
  • Agency: NICHD NIH HHS, United States
    Id: U54 HD079124
  • Agency: NIEHS NIH HHS, United States
    Id: DP1 ES024088
  • Agency: NIA NIH HHS, United States
    Id: R56 AG058663
  • Agency: NIEHS NIH HHS, United States
    Id: R56 ES028236

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This is a list of tools and resources that we have found mentioned in this publication.


SAMTOOLS (tool)

RRID:SCR_002105

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RRID:SCR_004633

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RRID:SCR_015687

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RRID:SCR_015987

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