Sequence, tissue distribution, and chromosomal localization of mRNA encoding a human glucose transporter-like protein.

Hirofumi Fukumoto(Howard Hughes Medical Institute), Susumu Seino(New York State Department of Health), Hiroo Imura(Howard Hughes Medical Institute), Yoshiki Seino(Howard Hughes Medical Institute), Roger L. Eddy(Howard Hughes Medical Institute), Yoshimitsu Fukushima(Howard Hughes Medical Institute), M.G. Byers(Howard Hughes Medical Institute), T.B. Shows(Howard Hughes Medical Institute), G I Bell(New York State Department of Health)
Proceedings of the National Academy of Sciences
August 1, 1988
Cited by 425Open Access
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Abstract

cDNA clones encoding a glucose transporter-like protein have been isolated from adult human liver and kidney cDNA libraries by cross-hybridization with the human HepG2/erythrocyte glucose transporter cDNA. Analysis of the sequence of this 524-amino acid glucose transporter-like protein indicates that it has 55.5% identity with the HepG2/erythrocyte glucose transporter as well as a similar structural organization. Studies of the tissue distribution of the mRNA coding for this glucose transporter-like protein in adult human tissues indicate that the highest amounts are present in liver with lower amounts in kidney and small intestine. The amounts of glucose transporter-like mRNA in other tissues, including colon, stomach, cerebrum, skeletal muscle, and adipose tissue, were below the level of sensitivity of our assay. The single-copy gene encoding this glucose transporter-like protein has been localized to the q26.1----q26.3 region of chromosome 3.


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