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Base excision repair

Definition

Base excision repair (BER) is a cellular mechanism, studied in the fields of biochemistry and genetics, that repairs damaged DNA throughout the cell cycle. It is responsible primarily for removing small, non-helix-distorting base lesions from the genome. The related nucleotide excision repair pathway repairs bulky helix-distorting lesions. BER is important for removing damaged bases that could otherwise cause mutations by mispairing or lead to breaks in DNA during replication. BER is initiated by DNA glycosylases, which recognize and remove specific damaged or inappropriate bases, forming AP sites. These are then cleaved by an AP endonuclease. The resulting single-strand break can then be processed by either short-patch or long-patch BER.

Related concepts

3-methyladenine5-Methylcytosine5-hydroxymethylcytosine5-methylcytosine7-methylguanosine8-Oxo-2'-deoxyguanosine8-Oxoguanine8-oxoguanineAPE1APE2APOBEC3GAP endonucleaseAP lyaseAP siteAdaptive responseAdenineApn1Apn2BRCA1BRIP1BiochemistryBloom syndrome proteinBrain-derived neurotrophic factorCRY1CRY2Cancer epigeneticsCarcinogenesisCognitionColon cancerColorectal cancerCpG siteCytosineDDB1DNA-3-methyladenine glycosylaseDNA PolymeraseDNA base flippingDNA demethylationDNA glycosylaseDNA ligaseDNA methylationDNA mismatch repairDNA oxidationDNA polymeraseDNA polymerase betaDNA polymerase lambdaDNA repairDNA replicationDeaminationDeletion (genetics)Directionality (molecular biology)Downregulation and upregulationERCC1ERCC2ERCC4ERCC5ERCC6ERCC8 (gene)Endonuclease IVEpigeneticsExcinucleaseExcision repair cross-complementingExonuclease IIIFANCAFANCBFANCD2FANCEFANCFFANCGFANCIFANCLFANCMFANC proteinsFEN1Fanconi anemia, complementation group CFear conditioningFlap endonucleaseGene promoterGene silencingGeneticsGlycosidic bondHelicaseHippocampusHomologous recombinationHomology directed repairHoogsteen base pairHost-cell reactivationHydantoinHypoxanthineIntronKu (protein)LexAMBD4MLH1MSH2MUTYHMedical Subject HeadingsMeiotic recombination checkpointMemoryMessenger RNAMicrohomology-mediated end joiningMutationNEIL1NeoplasmNeurobiological effects of physical exerciseNon-homologous end joiningNon-small-cell lung carcinomaNucleotide excision repairO-6-methylguanine-DNA methyltransferaseOkazaki fragmentOxoguanine glycosylaseP53PALB2PCNAPNKPPcrAPhotolyasePoly ADP ribose polymerasePostreplication repairProliferating cell nuclear antigenProtein O-GlcNAc transferasePyrimidineRAD23ARAD23BRAD51RecARecBCDRecF pathwayRecQ helicaseReplication protein ASMUG1SOS boxSOS responseSaccharomyces cerevisiaeSgs1Single-nucleotide polymorphismSlx4TRAMP complexTet methylcytosine dioxygenase 1Tet methylcytosine dioxygenase 2Tet methylcytosine dioxygenase 3ThymidineThymineThymine-DNA glycosylaseThymine glycolTranscription-coupled repairTransition (genetics)UracilUracil-DNA glycosylaseWerner syndrome ATP-dependent helicaseWhite blood cellXPAXPBXPC (gene)XRCC1Xanthine

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