Cloning and functional characterization of a new subtype of the amino acid transport system N.

Abstract

We have cloned a new subtype of the amino acid transport system N2 (SN2 or second subtype of system N) from rat brain. Rat SN2 consists of 471 amino acids and belongs to the recently identified glutamine transporter gene family that consists of system N and system A. Rat SN2 exhibits 63% identity with rat SN1. It also shows considerable sequence identity (50-56%) with the members of the amino acid transporter A subfamily. In the rat, SN2 mRNA is most abundant in the liver but is detectable in the brain, lung, stomach, kidney, testis, and spleen. When expressed in Xenopus laevis oocytes and in mammalian cells, rat SN2 mediates Na(+)-dependent transport of several neutral amino acids, including glycine, asparagine, alanine, serine, glutamine, and histidine. The transport process is electrogenic, Li(+) tolerant, and pH sensitive. The transport mechanism involves the influx of Na(+) and amino acids coupled to the efflux of H(+), resulting in intracellular alkalization. Proline, alpha-(methylamino)isobutyric acid, and anionic and cationic amino acids are not recognized by rat SN2.

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@article{Nakanishi2001CloningAF, title={Cloning and functional characterization of a new subtype of the amino acid transport system N.}, author={Takeshi Nakanishi and R Kekuda and Y . J . Fei and Tetsuya Hatanaka and Mitsuru Sugawara and Robert G. Martindale and Frederick H. Leibach and Puttur D. Prasad and Vadivel Ganapathy}, journal={American journal of physiology. Cell physiology}, year={2001}, volume={281 6}, pages={C1757-68} }