Characterization and Expression of Human HepG2/Erythrocyte Glucose-Transporter Gene

Author:

Fukumoto Hirofumi1,Seino Susumu1,Imura Hiroo1,Seino Yutaka1,Bell Graeme I1

Affiliation:

1. Howard Hughes Medical Institute and the Departments of Biochemistry and Molecular Biology and Medicine, The University of Chicago Chicago, Illinois Kyoto University School of Medicine Kyoto, Japan

Abstract

The human HepG2/erythrocyte glucose-transporter gene, including the promoter region, has been isolated and characterized. The gene, which is ∼35,000 base pairs, is interrupted by nine intervening sequences or introns. The sequence of the HepG2 glucose-transporter protein predicted from the gene sequence differs from that determined from the published cDNA sequence in having Leu rather than Phe at position 152. In addition, there are several other nucleotide differences between the gene and cDNA sequences in both the coding region and 3′-untranslated region that do not alter the amino acid sequence of the protein. The sequence of the promoter and the site of transcription initiation have also been determined. The promoter region includes a TATA motif and two binding sites for the transcription factor Spl as well as a sequence that is found in the promoter region of several phorbol ester–inducible genes.

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

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