TREX2

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Three prime repair exonuclease 2 is an enzyme that in humans is encoded by the TREX2 gene.[5][6]

PDBOrtholog search: PDBe RCSB
AliasesTREX2, three prime repair exonuclease 2
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TREX2
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesTREX2, three prime repair exonuclease 2
External IDsOMIM: 300370; MGI: 1346343; HomoloGene: 8046; GeneCards: TREX2; OMA:TREX2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_080701
NM_080699
NM_080700

NM_011907

RefSeq (protein)

NP_542432

NP_036037

Location (UCSC)Chr X: 153.44 – 153.47 MbChr X: 72.48 – 72.48 Mb
PubMed search[3][4]
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This gene encodes a protein with 3' exonuclease activity. Enzymes with this activity are involved in DNA replication, repair, and recombination. Similarity to an E. coli protein suggests that this enzyme may be a subunit of DNA polymerase III, which does not have intrinsic exonuclease activity.[6]

Newer research has determined that TREX2 is also involved in flap endonuclease activity, as detected in the context of inhibiting gene-editing nickases that generate an extension flap such as prime editors that do not usually create a double-stranded break. This function was first demonstrated in a thesis by Lung in 2021,[7] and replicated by Koeppel et al. in 2023.[8] Subsequently, TREX2 has become incorporated into fusion enzymes for genetic engineering by multiple research groups for the purposes of reducing off-target edits which include chromosomal translocations and mismatched insertions.[9][10]

Mutations in this gene may lead to Aicardi-Goutieres syndrome.

References

Further reading

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