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PMID: 2719857 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Synthesis and characterization of a bovine hexokinase 1 cDNA probe by mixed oligonucleotide primed amplification of cDNA using high complexity primer mixtures.

Biochemical medicine and metabolic biology ·Vol. 41 ·No. 2 ·1989-04-00 ·Pages 125-31

Griffin LD, MacGregor GR, Muzny DM, Harter J, Cook RG, McCabe ER

Abstract

Hexokinase (EC 2.7.1.1) catalyzes the first step in glucose metabolism, using ATP for the phosphorylation of glucose to glucose 6-phosphate. A portion of the HK1 gene was cloned by mixed oligonucleotide primer amplification of cDNA using primers of high complexity. The amino acid sequence for a partial fragment of bovine cardiac muscle HK was determined and used to create primer mixtures of 256- and 1024-fold complexity. Two products were generated from bovine cardiac muscle cDNA which show 82% nucleotide and 93% amino acid identity with a region of rat brain HK1 and cDNA. This work demonstrates that extension and amplification of cDNA probes may be successful even when amino acid sequence data indicate substantial codon degeneracy.

MeSH Terms
Amino Acid Sequence Animals Base Sequence Cattle Cloning, Molecular DNA/genetics DNA Probes Electrophoresis, Polyacrylamide Gel Gene Amplification Hexokinase/genetics Oligonucleotides Templates, Genetic
Chemicals
DNA Probes Oligonucleotides DNA Hexokinase
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Griffin L D
Institute for Molecular Genetics, Baylor College of Medicine, Houston, Texas 77030.
MacGregor G R
Muzny D M
Harter J
Cook R G
McCabe E R
Article Info
Journal
Biochemical medicine and metabolic biology
Abbr.
Biochem Med Metab Biol
ISSN
0885-4505
Published
1989-04-00
Pages
125-31
Language
English
Region
United States
NLM ID
8605718
Subset
IM
Grants
NICHD NIH HHS · R01 HD22563 · United States
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