4.6 Article

GLUT8, a novel member of the sugar transport facilitator family with glucose transport activity

Journal

JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 275, Issue 21, Pages 16275-16280

Publisher

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.275.21.16275

Keywords

-

Ask authors/readers for more resources

GLUTS is a novel glucose transporter-like protein that exhibits significant sequence similarity with the members of the sugar transport facilitator family (29.4% of amino acids identical with GLUT1), Human and mouse sequence (86.2% identical amino acids) comprise 12 putative membrane-spanning helices and several conserved motifs (sugar transporter signatures), which have previously been shown to be essential for transport activity, e.g. GRK in loop 2, PETPR in loop 6, QQLSGVN in helix 7, DRAGRR in loop 8, GWGPIPW in helix 10, and PETKG in the C-terminal tail. An expressed sequence tag (STS A005N15) corresponding with the 3'-untranslated region of GLUTS has previously been mapped to human chromosome 9, COS-7 cells transfected with GLUTS cDNA expressed a 42-kDa protein exhibiting specific, glucose-inhibitable cytochalasin B binding (K-D = 56.6 +/- 18 nM) and reconstitutable glucose transport activity (8.1 +/- 1.4 nmol/(mg protein x 10 s) versus 1.1 +/- 0.1 in control transfections), In human tissues, a 2.4-kilobase pair transcript was predominantly found in testis, but not in testicular carcinoma. Lower amounts of the mRNA were detected in most other tissues including skeletal muscle, heart, small intestine, and brain. GLUTS mRNA was found in testis from adult, but not from prepubertal rats; its expression in human testis was suppressed by estrogen treatment. It is concluded that GLUTS is a sugar transport facilitator with glucose transport activity and a hormonally regulated testicular function.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available