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March 1, 1990Journal of Lipid Research2,961 citationsOpen Access

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

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JHJames E. HixsonDVD.T. Vernier

Key Points

  • This research aims to develop a rapid method for typing common apolipoprotein E isoforms using restriction enzymes.
  • Utilized gene amplification of apolipoprotein E sequences at positions 112 and 158
  • Applied HhaI digestion on the amplification products
  • Conducted electrophoresis on polyacrylamide gels to separate the fragments.
  • Successfully distinguished between apolipoprotein E isoforms E2, E3, and E4 based on unique HhaI fragment patterns
  • Identified homozygotic and heterozygotic combinations clearly
  • Demonstrated a reliable method for genetic typing of apolipoprotein E.

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).

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Cite This Study

Hixson et al. (1990) studied this question.

synapsesocial.com/papers/6a0b9d8f9ead71e723c2013bhttps://doi.org/10.1016/s0022-2275(20)43176-1
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