TIME-RESOLVED FLUOROMETRY IN THE DIAGNOSIS OF LEBER HEREDITARY OPTIC NEURORETINOPATHY

被引:7
作者
HUOPONEN, K
JUVONEN, V
IITIA, A
DAHLEN, P
SIITARI, H
AULA, P
NIKOSKELAINEN, E
SAVONTAUS, ML
机构
[1] UNIV TURKU,DEPT MED GENET,SF-20520 TURKU,FINLAND
[2] UNIV TURKU,DEPT BIOCHEM,SF-20520 TURKU,FINLAND
[3] WALLAC OY,SF-20101 TURKU,FINLAND
[4] TURKU UNIV,CENT HOSP,DEPT OPHTHALMOL,SF-20500 TURKU,FINLAND
[5] UNIV TURKU,DEPT BIOL,SF-20500 TURKU,FINLAND
关键词
TIME-RESOLVED FLUOROMETRY; LHON; MTDNA; POINT MUTATION;
D O I
10.1002/humu.1380030106
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We have applied time-reserved fluorometry (TRF) to construct a DNA hybridization assay for the diagnosis of Leber hereditary optic neuroretinopathy (LHON). A rapid and reliable detection of the most prevalent mitochondrial DNA (mtDNA) point mutation associated with LHON is demonstrated. In addition, the TRF-method can be used in the quantification of heteroplasmy, a phenomenon commonly present in mtDNA mutations. The assay includes PCR amplification of a fragment encompassing the mutation site followed by hybridization reactions with allele-specific europium (Eu)-labelled oligonucleotide probes, A time-resolved fluorometer is used to measure the bound label. The TRF assay was successfully used to demonstrate the ND4/11778 mutation in patient samples, For quantification of heteroplasmy, synthetic target oligonucleotide mixtures with known ratios of wild-type and mutated sequences were used as standards to control the hybridization step. The assay allowed the detection of heteroplasmy ranging from 5 to 95%. This was also shown in a family with several heteroplasmic members. (C) 1994 Wiley-Liss, Inc.
引用
收藏
页码:29 / 36
页数:8
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