Direkt zum Inhalt
Merck

The XPV (xeroderma pigmentosum variant) gene encodes human DNA polymerase eta.

Nature (1999-06-29)
C Masutani, R Kusumoto, A Yamada, N Dohmae, M Yokoi, M Yuasa, M Araki, S Iwai, K Takio, F Hanaoka
ZUSAMMENFASSUNG

Xeroderma pigmentosum variant (XP-V) is an inherited disorder which is associated with increased incidence of sunlight-induced skin cancers. Unlike other xeroderma pigmentosum cells (belonging to groups XP-A to XP-G), XP-V cells carry out normal nucleotide-excision repair processes but are defective in their replication of ultraviolet-damaged DNA. It has been suspected for some time that the XPV gene encodes a protein that is involved in trans-lesion DNA synthesis, but the gene product has never been isolated. Using an improved cell-free assay for trans-lesion DNA synthesis, we have recently isolated a DNA polymerase from HeLa cells that continues replication on damaged DNA by bypassing ultraviolet-induced thymine dimers in XP-V cell extracts. Here we show that this polymerase is a human homologue of the yeast Rad30 protein, recently identified as DNA polymerase eta. This polymerase and yeast Rad30 are members of a family of damage-bypass replication proteins which comprises the Escherichia coli proteins UmuC and DinB and the yeast Rev1 protein. We found that all XP-V cells examined carry mutations in their DNA polymerase eta gene. Recombinant human DNA polymerase eta corrects the inability of XP-V cell extracts to carry out DNA replication by bypassing thymine dimers on damaged DNA. Together, these results indicate that DNA polymerase eta could be the XPV gene product.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
Taq-DNA-Polymerase aus Thermus aquaticus, with 10× PCR reaction buffer without MgCl2
Sigma-Aldrich
Taq-DNA-Polymerase aus Thermus aquaticus, with 10× PCR reaction buffer containing MgCl2
Sigma-Aldrich
DNA-Polymerase I aus E. coli lysogen für NM 964, buffered aqueous glycerol solution