Analysis of a human DNA excision repair gene involved in group A xeroderma pigmentosum and containing a zinc-finger domain - PubMed (original) (raw)
. 1990 Nov 1;348(6296):73-6.
doi: 10.1038/348073a0.
Affiliations
- PMID: 2234061
- DOI: 10.1038/348073a0
Analysis of a human DNA excision repair gene involved in group A xeroderma pigmentosum and containing a zinc-finger domain
K Tanaka et al. Nature. 1990.
Abstract
Xeroderma pigmentosum (XP) is an autosomal recessive disease, characterized by a high incidence of sunlight-induced skin cancer. Cells from people with this condition are hypersensitive to ultraviolet because of a defect in DNA repair. There are nine genetic complementation groups of XP, groups A-H and a variant. We have cloned the mouse DNA repair gene that complements the defect of group A, the XPAC gene. Here we report molecular cloning of human and mouse XPAC complementary DNAs. Expression of XPAC cDNA confers ultraviolet-resistance on several group A cell lines, but not on lines of other XP groups. Almost all group A lines tested showed abnormality or absence of XPAC messenger RNAs. These results indicate that a defective XPAC gene causes group A XP. The human and mouse XPAC genes are located on chromosome 9q34.1 and chromosome 4C2, respectively. Human XPAC cDNA encodes a protein of 273 amino acids with a zinc-finger motif.
Comment in
- Xeroderma pigmentosum. A gene for tumour prevention.
Wood RD, Lindahl T. Wood RD, et al. Nature. 1990 Nov 1;348(6296):13-4. doi: 10.1038/348013a0. Nature. 1990. PMID: 2234052 No abstract available.
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