Home LiteratureArticle Details
PMID: 1670750 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Analysis of the VNTR locus D1S80 by the PCR followed by high-resolution PAGE.

American journal of human genetics ·Vol. 48 ·No. 1 ·1991-01-00 ·Pages 137-44

Budowle B, Chakraborty R, Giusti AM, Eisenberg AJ, Allen RC

Abstract

Allelic data for the D1S80 locus was obtained by using the PCR and subsequent analysis with a high-resolution, horizontal PAGE technique and silver staining. Compared with RFLP analysis of VNTR loci by Southern blotting, the approach described in this paper offers certain advantages: (1) discrete allele resolution, (2) minimal measurement error, (3) correct genotyping of single-band VNTR patterns, (4) a nonisotopic assay, (5) a permanent record of the electrophoretic separation, and (6) reduced assay time. In a sample of 99 unrelated Caucasians, the D1S80 locus demonstrated a heterozygosity of 80.8% with 37 phenotypes and 16 alleles. The distribution of genotypes is in agreement with expected values according to the Hardy-Weinberg equilibrium. Furthermore, the observed number of alleles and the level of heterozygosity, obtained through the protocol described here, were congruent with each other in accordance with the expectation of a mutation-drift equilibrium model for a single, homogeneous, random-mating population. Therefore, the analysis of D1S80 and similar VNTR loci by amplified fragment length polymorphism (AMP-FLP) may prove useful as models for population genetic issues for VNTR loci analyzed by RFLP typing via Southern blotting.

MeSH Terms
Blotting, Southern DNA/genetics Electrophoresis, Polyacrylamide Gel Genetic Markers Humans Molecular Sequence Data Oligonucleotide Probes Polymerase Chain Reaction Polymorphism, Restriction Fragment Length Repetitive Sequences, Nucleic Acid
Chemicals
Genetic Markers Oligonucleotide Probes DNA
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Budowle B
Forensic Science Research and Training Center, Federal Bureau of Investigation Academy, Quantico, VA 22135.
Chakraborty R
Giusti A M
Eisenberg A J
Allen R C
References (11)
11 references, click to expand
  1. Modifications to improve the effectiveness of restriction fragment length polymorphism typing.
    Appl Theor Electrophor. 1990;1(4):181-7 PMID: 1982991
  2. Polymerase chain reaction amplification products separated on rehydratable polyacrylamide gels and stained with silver.
    Biotechniques. 1989 Jul-Aug;7(7):736-44 PMID: 2483661
  3. Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia.
    Science. 1985 Dec 20;230(4732):1350-4 PMID: 2999980
  4. Amplification of a highly polymorphic VNTR segment by the polymerase chain reaction.
    Nucleic Acids Res. 1989 Mar 11;17(5):2140 PMID: 2928126
  5. Rapid typing of tandemly repeated hypervariable loci by the polymerase chain reaction: application to the apolipoprotein B 3' hypervariable region.
    Proc Natl Acad Sci U S A. 1989 Jan;86(1):212-6 PMID: 2911570
  6. Detection of specific sequences among DNA fragments separated by gel electrophoresis.
    J Mol Biol. 1975 Nov 5;98(3):503-17 PMID: 1195397
  7. Isolation and mapping of a polymorphic DNA sequence (pMCT118) on chromosome 1p [D1S80].
    Nucleic Acids Res. 1988 Oct 11;16(19):9364 PMID: 2902591
  8. Population amalgamation and genetic variation: observations on artificially agglomerated tribal populations of Central and South America.
    Am J Hum Genet. 1988 Nov;43(5):709-25 PMID: 3189334
  9. Mitochondrial DNA polymorphism reveals hidden heterogeneity within some Asian populations.
    Am J Hum Genet. 1990 Jul;47(1):87-94 PMID: 2349953
  10. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity.
    Anal Biochem. 1983 Jul 1;132(1):6-13 PMID: 6312838
  11. High-resolution analysis of a hypervariable region in the human apolipoprotein B gene.
    Am J Hum Genet. 1989 Sep;45(3):458-64 PMID: 2773938
Article Info
Journal
American journal of human genetics
Abbr.
Am J Hum Genet
ISSN
0002-9297
Published
1991-01-00
Pages
137-44
Language
English
Region
United States
NLM ID
0370475
PMCID
PMC1682756
Subset
IM
Grants
NIGMS NIH HHS · GM41399 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]