DNA repair mechanisms in dividing and non-dividing cells

Teruaki Iyama1, David M Wilson

  • 1Laboratory of Molecular Gerontology, National Institute on Aging, National Institutes of Health, 251 Bayview Boulevard, Baltimore, MD 21224, USA.

DNA Repair
|May 21, 2013
PubMed

Insights

Cells possess DNA repair pathways to fix DNA damage, preventing genome instability and diseases like cancer. This review examines DNA repair in dividing versus non-dividing cells, focusing on neurological disease development.

Area of Science:

  • Molecular Biology
  • Genetics
  • Cell Biology

Background:

  • DNA damage from internal and external sources can cause genome instability and diseases.
  • Cells have evolved multiple DNA repair pathways to resolve DNA lesions.
  • Understanding DNA repair requires considering the cellular context, such as dividing versus non-dividing cells.

Purpose of the Study:

  • To describe the molecular mechanisms of various DNA repair pathways.
  • To review the roles of DNA repair pathways in non-dividing and dividing cells.
  • To explore how DNA repair pathways influence neurological disease development.

Main Methods:

  • Literature review of molecular mechanisms of DNA repair.
  • Analysis of DNA repair pathway functions in different cell types.
  • Examination of the link between DNA repair and neurological disorders.

Main Results:

  • Multiple DNA repair pathways exist to counteract DNA damage.
  • The function and importance of DNA repair pathways differ between dividing and non-dividing cells.
  • Dysfunctional DNA repair is implicated in neurological diseases.

Conclusions:

  • DNA repair pathways are crucial for maintaining genome integrity and preventing disease.
  • Cellular context significantly impacts DNA repair mechanisms and outcomes.
  • Targeting DNA repair pathways may offer therapeutic strategies for neurological diseases.
Keywords:
6-4PPs8-oxoguanine DNA glycosylaseAOA1APAP endonuclease 1APE1APTXATMCPDsCSCSRCockayne syndromeDARDNA double strand break repairDNA polymerase βDNA repairDNA single strand break repairDNA single strand breaksDNA-PKcsDNA-dependent protein kinase catalytic subunitDSBRDividing and non-dividingERCC1Endogenous DNA damageFEN1GG-NERHNPCCHRIRMAPMCSZMGMTMMRMPGMUTYHMUTYH-associated polyposisN-methylpurine-DNA glycosylaseNEIL1NERNHEJNSCNTH1Neural cellsNeurological disorderO(6)-methylguanine-DNA methyltransferaseOGG1PARP1PCNAPGPNKPPUAPol βRFCRNA polymeraseRNAPRPASCAN1SCIDSDSASSASSBRSSBsTC-NERTDP1TFIIHTOP1TTDTop1 cleavage complexTop1ccUNGX-ray repair cross-complementing protein 1XPXRCC1aprataxinapurinic/apyrimidinicataxia telangiectasia mutatedataxia with ocular motor apraxia 1class switch recombinationcyclobutane pyrimidine dimersdRPdeoxyribose-5-phosphateendonuclease III-like 1endonuclease VIII-like 1excision repair cross complementing 1flap endonuclease 1global genome-NERhereditary nonpolyposis colorectal cancerhomologous recombinationhuman mutY homologionizing radiationmicrocephaly with early-onset, intractable seizures and developmental delaymismatch repairneural stem cellsnonhomologous end joiningnucleotide excision repairphospho-α,β-unsaturated aldehydephosphoglycolatepoly(ADP-ribose) polymerase-1polynucleotide kinase 3′-phosphataseproliferating cellular nuclear antigenpyrimidine-(6,4)-pyrimidone photoproducts.replication factor Creplication protein Asevere combined immunodeficientsingle-strand annealingspinocerebellar ataxia with axonal neuropathy-1synthesis-dependent strand annealingtopoisomerase 1transcription domains-associated repairtranscription factor II Htranscription-coupled NERtrichothiodystrophytyrosyl-DNA phosphodiesterase 1uracil-DNA glycosylasexeroderma pigmentosum

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