Taylor E M, Broughton B C, Botta E, Stefanini M, Sarasin A, Jaspers N G, Fawcett H, Harcourt S A, Arlett C F, Lehmann A R
Medical Research Council Cell Mutation Unit, Sussex University, Falmer, Brighton BN1 9RR, United Kingdom.
Proc Natl Acad Sci U S A. 1997 Aug 5;94(16):8658-63. doi: 10.1073/pnas.94.16.8658.
The xeroderma pigmentosum group D (XPD) protein has a dual function, both in nucleotide excision repair of DNA damage and in basal transcription. Mutations in the XPD gene can result in three distinct clinical phenotypes, XP, trichothiodystrophy (TTD), and XP with Cockayne syndrome. To determine if the clinical phenotypes of XP and TTD can be attributed to the sites of the mutations, we have identified the mutations in a large group of TTD and XP-D patients. Most sites of mutations differed between XP and TTD, but there are three sites at which the same mutation is found in XP and TTD patients. Since the corresponding patients were all compound heterozygotes with different mutations in the two alleles, the alleles were tested separately in a yeast complementation assay. The mutations which are found in both XP and TTD patients behaved as null alleles, suggesting that the disease phenotype was determined by the other allele. If we eliminate the null mutations, the remaining mutagenic pattern is consistent with the site of the mutation determining the phenotype.
着色性干皮病D组(XPD)蛋白具有双重功能,既参与DNA损伤的核苷酸切除修复,又参与基础转录。XPD基因突变可导致三种不同的临床表型:着色性干皮病(XP)、毛发硫营养不良(TTD)以及伴有科凯恩综合征的XP。为了确定XP和TTD的临床表型是否可归因于突变位点,我们在一大群TTD和XP-D患者中鉴定了突变。XP和TTD的大多数突变位点不同,但有三个位点在XP和TTD患者中发现了相同的突变。由于相应患者均为两个等位基因具有不同突变的复合杂合子,因此在酵母互补试验中分别对这些等位基因进行了检测。在XP和TTD患者中均发现的突变表现为无效等位基因,这表明疾病表型由另一个等位基因决定。如果我们排除无效突变,那么剩余的诱变模式与决定表型的突变位点是一致的。