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PMID: 2341813 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Restriction isotyping of human apolipoprotein E by gene amplification and cleavage with HhaI.

Journal of lipid research ·Vol. 31 ·No. 3 ·1990-03-00 ·Pages 545-8

Hixson JE, Vernier DT

Abstract

We have used restriction isotyping (restriction enzyme isoform genotyping) for rapid typing of common apolipoprotein E isoforms (E2, E3, E4). ApoE restriction isotyping used oligonucleotides to amplify apolipoprotein E gene sequences containing amino acid positions 112 and 158. The amplification products were digested with HhaI and subjected to electrophoresis on polyacrylamide gels. Each of the isoforms was distinguished by a unique combination of HhaI fragment sizes that enabled unambiguous typing of all homozygotic and heterozygotic combinations. HhaI cleaves at GCGC encoding 112arg (E4) and 158arg (E3, E4), but does not cut at GTGC encoding 112cys (E2, E3) and 158cys (E2).

MeSH Terms
Amino Acid Sequence Apolipoproteins E/genetics,isolation & purification Base Sequence DNA/isolation & purification,metabolism Deoxyribonucleases, Type II Site-Specific/metabolism Gene Amplification Humans Leukocytes/metabolism Molecular Sequence Data Polymerase Chain Reaction Polymorphism, Genetic
Chemicals
Apolipoproteins E DNA Deoxyribonucleases, Type II Site-Specific GCGC-specific type II deoxyribonucleases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Hixson J E
Department of Genetics, Southwest Foundation for Biomedical Research, San Antonio, TX 78284.
Vernier D T
Article Info
Journal
Journal of lipid research
Abbr.
J Lipid Res
ISSN
0022-2275
Published
1990-03-00
Pages
545-8
Language
English
Region
United States
NLM ID
0376606
Subset
IM
Grants
NHLBI NIH HHS · HL-28972 · United States
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