L. Riou et al., The relative expression of mutated XPB genes results in xeroderma pigmentosum/Cockayne's syndrome or trichothiodystrophy cellular phenotypes, HUM MOL GEN, 8(6), 1999, pp. 1125-1133
The human XPB DNA helicase is a subunit of the DNA repair/basal transcripti
on factor TFIIH, involved in early steps of the nucleotide excision repair
pathway. Two distinct clinical phenotypes, xeroderma pigmentosum associated
with Cockayne's syndrome (XP/ CS) and trichothiodystrophy (TTD), can be du
e to mutations in the XPB gene. In the present work, we studied cellular DN
A repair properties of skin fibroblasts from two patients mutated in the XP
B gene: an XP/CS patient cell (XPCS2BA) with a T296C (F99S) transition and
a TTD patient cell (TTD6VI) exhibiting an A355C (T119P) transversion. Both
cells are clearly associated with different levels of alterations in their
response to UV light. To establish the relationship between the relative ex
pression level of these two alleles and DNA repair properties, we transfect
ed SV40-transformed XPCS2BA (XPCS2BASV) cells with a plasmid (pTTD6VI) carr
ying the XPB-A355C cDNA and examined DNA repair properties after UV irradia
tion (cell survival, unscheduled DNA synthesis and kinetics of photoproduct
removal) in stable transfectants. We isolated three clones, which express
the XPB-A355C gene (CI-5) or the XPB-T296C gene (CI-14) or both genes (CI-1
9), This constitutes a model system allowing us to correlate the relative e
xpression levels of the XPB-A355C (TTD) and XPB-T296C (XP/CS) genes with va
rious DNA repair properties. Overexpression of the XPB-A355C (TTD) gene in
an XP/CS cell gives rise to a cellular phenotype of increased repair simila
r to that of TTD6VI cells, while equal expression of the two mutated genes
leads to an intermediate cellular phenotype between XP/CS and TTD.