Molecular cloning of a novel brain-type Na+-dependent inorganic phosphate cotransporter

被引:228
作者
Aihara, Y
Mashima, H
Onda, H
Hisano, S
Kasuya, H
Hori, T
Yamada, S
Tomura, H
Yamada, Y
Inoue, I
Kojima, I
Takeda, J
机构
[1] Gunma Univ, Inst Mol & Cellular Regulat, Dept Cell Biol, Mol Genet Lab, Gunma 3718512, Japan
[2] Gunma Univ, Inst Mol & Cellular Regulat, Dept Cell Biol, Lab Cell Physiol, Gunma 3718512, Japan
[3] Tokyo Womens Med Univ, Inst Neurol, Dept Neurosurg, Tokyo, Japan
[4] Univ Tsukuba, Inst Basic Med Sci, Dept Anat, Ibaraki, Osaka, Japan
[5] Kyoto Univ, Grad Sch Med, Dept Metab & Clin Nutr, Kyoto, Japan
关键词
cDNA cloning; phosphate transport; structurally related family; neuron;
D O I
10.1046/j.1471-4159.2000.0742622.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have isolated a human cDNA encoding a protein, designated DNPI, that shows 82% amino acid identity and 92% similarity to the human brain-specific Na+-dependent inorganic phosphate (Na+/P-i) cotransporter (BNPI), which is localized exclusively to neuron-rich regions. Expression of DNPI mRNA in Xenopus oocytes resulted in a significant increase in Na+-dependent P-i transport, indicating that DNPI is a novel Na+/P-i cotransporter. Northern blot analysis shows that DNPI mRNA is expressed predominantly in brain, where the highest levels are observed in medulla, substantia nigra, subthalamic nucleus, and thalamus, all of which express BNPI mRNA at low levels. In contrast, DNPI mRNA is expressed at low levels in cerebellum and hippocampus, where BNPI mRNA is expressed at high levels. No hybridizing signal for DNPI mRNA is observed in the glia-rich region of corpus callosum. In other regions examined, both mRNAs are moderately or highly expressed. These results indicate that BNPI and DNPI, which coordinate Na+-dependent P-i transport in the neuron-rich regions of the brain, may form a new class within the Na+/P-i cotransporter family.
引用
收藏
页码:2622 / 2625
页数:4
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