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Human liver glucokinase gene: Cloning and sequence determination of two alternatively spliced cDNAs

Journal Article · · Proceedings of the National Academy of Sciences of the United States of America; (United States)
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  1. Washington Univ., St. Louis, MO (United States)
A human liver glucokinase was isolated from a liver cDNA library. This cDNA (hLGLK1) appeared to be full length as its size was consistent with a single 2.8-kilobase (kb) glucokinase mRNA on Northern blot analysis of liver poly(A){sup +}RNA. The cDNA contained an open reading frame of 1392 bp that predicted a protein of 464 amino acids and a molecular mass of 52 kDa; this protein has 97% identity to rat liver glucokinase. Fourteen residues on the amino terminus of the predicted human liver glucokinase, however, differed completely from those of the predicted rat liver enzyme and could be explained by alternative splicing of a 124-bp cassette exon in human cDNA. A second glucokinase cDNA (hLGLK2), missing the 124-bp cassette exon, was isolated by PCR amplification of human liver cDNA. These results suggested that the alternative splicing of a cassette exon in hLGLK1 resulted in an mRNA with an upstream initiator codon and reduced function. The relative biological activity of the two isoforms of human glucokinase and their possible developmental and/or metabolic regulation remain to be determined.
OSTI ID:
5604248
Journal Information:
Proceedings of the National Academy of Sciences of the United States of America; (United States), Journal Name: Proceedings of the National Academy of Sciences of the United States of America; (United States) Vol. 88:16; ISSN 0027-8424; ISSN PNASA
Country of Publication:
United States
Language:
English