Abstract
A simple primer extension method for detecting nucleotide differences is based on the substitution of mobility-shifting analogs for natural nucleotides (1). This technique can detect any single-base difference that might occur including previously unknown mutations or polymorphisms. Two technical limitations of the original procedure have now been addressed. First, switching to Thermococcus litoralis DNA polymerase has eliminated variability believed to be due to the addition of an extra, non-templated base to the 3' end of DNA by Taq DNA polymerase. Second, with the analogs used in the original study, the mobility shift induced by a single base change can usually be resolved only in DNA segments 200 nt or smaller. This size limitation has been overcome by synthesizing biotinylated nucleotides with extraordinarily long linker arms (36 atom backbone). Using these new analogs and conventional sequencing gels (0.4 mm thick), mutations in the human beta-hexosaminidase alpha and CYP2D6 genes have been detected in DNA segments up to 300 nt in length. By using very thin (0.15 mm) gels, single-base polymorphisms in the human APOE gene have been detected in 500-nt segments.
MeSH Terms
Base Sequence
Biotin/analogs & derivatives,chemical synthesis
Cytochrome P-450 CYP2D6
Cytochrome P-450 Enzyme System/genetics
Deoxyadenine Nucleotides/chemical synthesis
Deoxycytosine Nucleotides/chemical synthesis
Deoxyuracil Nucleotides/chemical synthesis
Genetic Carrier Screening
Humans
Indicators and Reagents
Introns
Mixed Function Oxygenases/genetics
Molecular Sequence Data
Mutation
Oligodeoxyribonucleotides
Polymerase Chain Reaction/methods
Polymorphism, Genetic
Tay-Sachs Disease/genetics
beta-N-Acetylhexosaminidases/genetics
Chemicals
Deoxyadenine Nucleotides
Deoxycytosine Nucleotides
Deoxyuracil Nucleotides
Indicators and Reagents
Oligodeoxyribonucleotides
biotin-36-dUTP
biotin-36-dCTP
biotin-36-dc7ATP
Biotin
Cytochrome P-450 Enzyme System
Mixed Function Oxygenases
Cytochrome P-450 CYP2D6
beta-N-Acetylhexosaminidases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Livak K J
Du Pont Merck Pharmaceutical Company, Experimental Station, Wilmington, DE 19880-0328.
Hobbs F W
Zagursky R J
References (23)
23 references, click to expand
-
The mutations in Ashkenazi Jews with adult GM2 gangliosidosis, the adult form of Tay-Sachs disease.
Science. 1989 Mar 17;243(4897):1471-4
PMID: 2522679
-
A system for rapid DNA sequencing with fluorescent chain-terminating dideoxynucleotides.
Science. 1987 Oct 16;238(4825):336-41
PMID: 2443975
-
The major defect in Ashkenazi Jews with Tay-Sachs disease is an insertion in the gene for the alpha-chain of beta-hexosaminidase.
J Biol Chem. 1988 Dec 15;263(35):18587-9
PMID: 2848800
-
Nucleotide sequence and structure of the human apolipoprotein E gene.
Proc Natl Acad Sci U S A. 1985 May;82(10):3445-9
PMID: 2987927
-
Apolipoprotein E polymorphism and atherosclerosis.
Arteriosclerosis. 1988 Jan-Feb;8(1):1-21
PMID: 3277611
-
Detection of single base substitutions in total genomic DNA.
Nature. 1985 Feb 7-13;313(6002):495-8
PMID: 3969155
-
Rapid DNA sequencing by horizontal ultrathin gel electrophoresis.
Nucleic Acids Res. 1991 Aug 11;19(15):4121-6
PMID: 1870968
-
Genotyping of poor metabolisers of debrisoquine by allele-specific PCR amplification.
Lancet. 1990 Sep 1;336(8714):529-32
PMID: 1975039
-
Multiple mutations of the human cytochrome P450IID6 gene (CYP2D6) in poor metabolizers of debrisoquine. Study of the functional significance of individual mutations by expression of chimeric genes.
J Biol Chem. 1990 Oct 5;265(28):17209-14
PMID: 2211621
-
Novel non-templated nucleotide addition reactions catalyzed by procaryotic and eucaryotic DNA polymerases.
Nucleic Acids Res. 1988 Oct 25;16(20):9677-86
PMID: 2460825
-
The human debrisoquine 4-hydroxylase (CYP2D) locus: sequence and identification of the polymorphic CYP2D6 gene, a related gene, and a pseudogene.
Am J Hum Genet. 1989 Dec;45(6):889-904
PMID: 2574001
-
Attachment of a 40-base-pair G + C-rich sequence (GC-clamp) to genomic DNA fragments by the polymerase chain reaction results in improved detection of single-base changes.
Proc Natl Acad Sci U S A. 1989 Jan;86(1):232-6
PMID: 2643100
-
Mutation detection using nucleotide analogs that alter electrophoretic mobility.
Nucleic Acids Res. 1989 Oct 11;17(19):7779-84
PMID: 2798127
-
Human beta-hexosaminidase alpha chain: coding sequence and homology with the beta chain.
Proc Natl Acad Sci U S A. 1985 Dec;82(23):7830-4
PMID: 2933746
-
Genotyping and sequence analysis of apolipoprotein E isoforms.
Genomics. 1988 Nov;3(4):373-9
PMID: 3243553
-
Reactivity of cytosine and thymine in single-base-pair mismatches with hydroxylamine and osmium tetroxide and its application to the study of mutations.
Proc Natl Acad Sci U S A. 1988 Jun;85(12):4397-401
PMID: 3260032
-
Splice junction mutation in some Ashkenazi Jews with Tay-Sachs disease: evidence against a single defect within this ethnic group.
Proc Natl Acad Sci U S A. 1988 Jun;85(11):3955-9
PMID: 3375249
-
Detection of single base substitutions by ribonuclease cleavage at mismatches in RNA:DNA duplexes.
Science. 1985 Dec 13;230(4731):1242-6
PMID: 4071043
-
Enzymatic synthesis of biotin-labeled polynucleotides: novel nucleic acid affinity probes.
Proc Natl Acad Sci U S A. 1981 Nov;78(11):6633-7
PMID: 6273878
-
Improvements of DNA sequencing gels.
Anal Biochem. 1981 Aug;115(2):450-7
PMID: 7304971
-
Detecting single base substitutions as heteroduplex polymorphisms.
Genomics. 1992 Feb;12(2):301-6
PMID: 1740339
-
Nonradioactive labeling of oligonucleotides in vitro with the hapten digoxigenin by tailing with terminal transferase.
Anal Biochem. 1991 Jan;192(1):222-31
PMID: 2048725
-
Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction.
Genomics. 1989 Nov;5(4):874-9
PMID: 2687159