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Mol Cell Biol
1992 Dec 01;1212:5281-7. doi: 10.1128/mcb.12.12.5281-5287.1992.
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Chinese hamster ovary mRNA-dependent, Na(+)-independent L-leucine transport in Xenopus laevis oocytes.
Su TZ
,
Logsdon CD
,
Oxender DL
.
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In freshly prepared uninjected folliculated oocytes, Na(+)-independent leucine uptake is mediated predominantly by a system L-like transport system. Removal of follicular cells, however, results in an irreversible loss of this transport activity. When total poly(A)+ mRNA derived from Chinese hamster ovary (CHO) cells was injected into prophase-arrested stage V or VI Xenopus laevis oocytes, enhanced expression of Na(+)-independent leucine transport was observed. The injected mRNAs associated with increased levels of leucine uptake were between 2 and 3 kb in length. The newly expressed leucine transport activity exhibited important differences from the known characteristics of system L, which is the dominant Na(+)-independent leucine transporter in CHO cells as well as in freshly isolated folliculated oocytes. The CHO mRNA-dependent leucine uptake in oocytes was highly sensitive to the cationic amino acids lysine, arginine, and and ornithine (> 95% inhibition). As with the leucine uptake, an enhanced lysine uptake was also observed in size-fractionated CHO mRNA-injected oocytes. The uptakes of leucine and lysine were mutually inhibitable, suggesting that the newly expressed transporter was responsible for uptakes of both leucine and lysine. The inhibition of uptake of lysine by leucine was Na+ independent, thus clearly distinguishing it from the previously reported endogenous system y+ activity. Furthermore, the high sensitivity to tryptophan of the CHO mRNA-dependent leucine transport was in sharp contrast to the properties of the recently cloned leucine transport-associated gene from rat kidneytissue, although leucine transport from both sources was sensitive to cationic amino acids. Our results suggest that there may be a family of leucine transporters operative in different tissues and possibly under different conditions.
Aoshima,
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1988, Pubmed,
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Aoshima,
Expression of amino acid transport systems in Xenopus oocytes injected with mRNA of rat small intestine and kidney.
1988,
Pubmed
,
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Aviv,
Purification of biologically active globin messenger RNA by chromatography on oligothymidylic acid-cellulose.
1972,
Pubmed
Bertran,
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1992,
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,
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Bertran,
Stimulation of system y(+)-like amino acid transport by the heavy chain of human 4F2 surface antigen in Xenopus laevis oocytes.
1992,
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,
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Blakely,
Cloning and expression of a functional serotonin transporter from rat brain.
1991,
Pubmed
Boerner,
Polarity of neutral amino acid transport and characterization of a broad specificity transport activity in a kidney epithelial cell line, MDCK.
1986,
Pubmed
Campa,
Characterization of neutral and cationic amino acid transport in Xenopus oocytes.
1989,
Pubmed
,
Xenbase
Christensen,
Role of amino acid transport and countertransport in nutrition and metabolism.
1990,
Pubmed
Christensen,
Organic ion transport during seven decades. The amino acids.
1984,
Pubmed
Christensen,
On the strategy of kinetic discrimination of amino acid transport systems.
1985,
Pubmed
Coady,
Expression of mammalian renal transporters in Xenopus laevis oocytes.
1990,
Pubmed
,
Xenbase
Collarini,
Mechanisms of transport of amino acids across membranes.
1987,
Pubmed
Guastella,
Cloning, expression, and localization of a rat brain high-affinity glycine transporter.
1992,
Pubmed
,
Xenbase
Guastella,
Cloning and expression of a rat brain GABA transporter.
1990,
Pubmed
,
Xenbase
Gurdon,
Use of frog eggs and oocytes for the study of messenger RNA and its translation in living cells.
1971,
Pubmed
,
Xenbase
Hediger,
Expression of size-selected mRNA encoding the intestinal Na/glucose cotransporter in Xenopus laevis oocytes.
1987,
Pubmed
,
Xenbase
Hediger,
Expression cloning and cDNA sequencing of the Na+/glucose co-transporter.
,
Pubmed
,
Xenbase
Kilty,
Cloning and expression of a cocaine-sensitive rat dopamine transporter.
1991,
Pubmed
Kim,
Transport of cationic amino acids by the mouse ecotropic retrovirus receptor.
1991,
Pubmed
,
Xenbase
Kwon,
Size selected mRNA induces expression of P-aminohippurate transport in Xenopus oocytes.
1989,
Pubmed
,
Xenbase
Pacholczyk,
Expression cloning of a cocaine- and antidepressant-sensitive human noradrenaline transporter.
1991,
Pubmed
Palacin,
Expression of rat liver Na+/L-alanine co-transport in Xenopus laevis oocytes. Effect of glucagon in vivo.
1990,
Pubmed
,
Xenbase
Puissant,
An improvement of the single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction.
1990,
Pubmed
Schwarz,
Characteristics of the Na+/K+-ATPase from Torpedo californica expressed in Xenopus oocytes: a combination of tracer flux measurements with electrophysiological measurements.
1988,
Pubmed
,
Xenbase
Shotwell,
Isolation of Chinese hamster ovary cell mutants defective in the regulation of leucine transport.
1983,
Pubmed
Sigel,
Use of Xenopus oocytes for the functional expression of plasma membrane proteins.
1990,
Pubmed
,
Xenbase
Tarnuzzer,
Expression of the mammalian system A neutral amino acid transporter in Xenopus oocytes.
1990,
Pubmed
,
Xenbase
Tate,
Expression of the mammalian Na+-independent L system amino acid transporter in Xenopus laevis oocytes.
1989,
Pubmed
,
Xenbase
Tate,
Expression cloning of a Na(+)-independent neutral amino acid transporter from rat kidney.
1992,
Pubmed
,
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Taylor,
Expression of rat liver glutamine transporters in Xenopus laevis oocytes.
1992,
Pubmed
,
Xenbase
Thomas,
Indications of spatial relations among structures recognizing amino acids and Na+ at a transport receptor site.
1970,
Pubmed
Thomas,
Structural selectivity in interaction of neutral amino acids and alkali metal ions with a cationic amino acid transport system.
1971,
Pubmed
Van Winkle,
Inhibition of transport system b0,+ in blastocysts by inorganic and organic cations yields insight into the structure of its amino acid receptor site.
1990,
Pubmed
Van Winkle,
Changes in the activities of amino acid transport systems b0,+ and L during development of preimplantation mouse conceptuses.
1990,
Pubmed
Van Winkle,
Na+-independent transport of basic and zwitterionic amino acids in mouse blastocysts by a shared system and by processes which distinguish between these substrates.
1988,
Pubmed
Van Winkle,
Na+-dependent transport of basic, zwitterionic, and bicyclic amino acids by a broad-scope system in mouse blastocysts.
1985,
Pubmed
Weissbach,
Evidence for two Na+-independent neutral amino acid transport systems in primary cultures of rat hepatocytes. Time-dependent changes in activity.
1982,
Pubmed
Wells,
Cloning of a rat kidney cDNA that stimulates dibasic and neutral amino acid transport and has sequence similarity to glucosidases.
1992,
Pubmed
,
Xenbase
White,
Cationic amino acid transport into cultured animal cells. II. Transport system barely perceptible in ordinary hepatocytes, but active in hepatoma cell lines.
1982,
Pubmed
Yamauchi,
Cloning of a Na(+)- and Cl(-)-dependent betaine transporter that is regulated by hypertonicity.
1992,
Pubmed
,
Xenbase
Young,
Topographical similarities between harmaline inhibition sites on Na+-dependent amino acid transport system ASC in human erythrocytes and Na+-independent system asc in horse erythrocytes.
1988,
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