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Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1988 Dec;85(24):9846–9850. doi: 10.1073/pnas.85.24.9846

Expression of neurotransmitter transport from rat brain mRNA in Xenopus laevis oocytes.

R D Blakely 1, M B Robinson 1, S G Amara 1
PMCID: PMC282878  PMID: 2904681

Abstract

To permit a molecular characterization of neurotransmitter transporter proteins, we have studied uptake activities induced in Xenopus laevis oocytes after injection of adult rat forebrain, cerebellum, brainstem, and spinal cord poly(A)+ RNA. L-Glutamate uptake could be observed as early as 24 hr after injection, was linearly related to the quantity of mRNA injected, and could be induced after injection of as little as 1 ng of cerebellar mRNA. Transport of radiolabeled L-glutamate, gamma-aminobutyric acid, glycine, dopamine, serotonin, and choline could be measured in single microinjected oocytes with a regional profile consistent with the anatomical distribution of particular neurotransmitter synthesizing soma. Forebrain L-glutamate and dopamine uptake, as well as cerebellar L-glutamate transport, were found to be Na+-dependent. Cerebellar mRNA-induced L-glutamate transport was both time and temperature-dependent, was saturable by substrate, suggesting a single activity with an apparent transport Km of 14.2 microM and a Vmax of 15.2 pmol/hr per oocyte, and was sensitive to inhibitors of brain L-glutamate transport. Thus, the oocyte L-glutamate transport induced by injection of adult rat cerebellar mRNA appears essentially identical to the high-affinity, Na+-dependent L-glutamate uptake found in brain slices and nerve terminals. Experiments with size-fractionated cerebellar mRNA reveal single, comigrating peaks for cerebellar L-glutamate and gamma-aminobutyric acid transport, with peak activity obtained in fractions of approximately 2.7 kilobases, suggesting the presence of single or similarly sized mRNAs encoding each of these activities.

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Selected References

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  1. Aoshima H., Tomita K., Sugio S. Expression of amino acid transport systems in Xenopus oocytes injected with mRNA of rat small intestine and kidney. Arch Biochem Biophys. 1988 Aug 15;265(1):73–81. doi: 10.1016/0003-9861(88)90372-4. [DOI] [PubMed] [Google Scholar]
  2. Axelrod J. Noradrenaline: fate and control of its biosynthesis. Science. 1971 Aug 13;173(3997):598–606. doi: 10.1126/science.173.3997.598. [DOI] [PubMed] [Google Scholar]
  3. Balcar V. J., Johnston G. A. The structural specificity of the high affinity uptake of L-glutamate and L-aspartate by rat brain slices. J Neurochem. 1972 Nov;19(11):2657–2666. doi: 10.1111/j.1471-4159.1972.tb01325.x. [DOI] [PubMed] [Google Scholar]
  4. Bennett J. P., Jr, Logan W. J., Snyder S. H. Amino acids as central nervous transmitters: the influence of ions, amino acid analogues, and ontogeny on transport systems for L-glutamic and L-aspartic acids and glycine into central nervous synaptosomes of the rat. J Neurochem. 1973 Dec;21(6):1533–1550. doi: 10.1111/j.1471-4159.1973.tb06037.x. [DOI] [PubMed] [Google Scholar]
  5. Coyle J. T., Snyder S. H. Catecholamine uptake by synaptosomes in homogenates of rat brain: stereospecificity in different areas. J Pharmacol Exp Ther. 1969 Dec;170(2):221–231. [PubMed] [Google Scholar]
  6. Fagg G. E., Lane J. D. The uptake and release of putative amino acid neurotransmitters. Neuroscience. 1979;4(8):1015–1036. doi: 10.1016/0306-4522(79)90185-4. [DOI] [PubMed] [Google Scholar]
  7. Ferkany J., Coyle J. T. Heterogeneity of sodium-dependent excitatory amino acid uptake mechanisms in rat brain. J Neurosci Res. 1986;16(3):491–503. doi: 10.1002/jnr.490160305. [DOI] [PubMed] [Google Scholar]
  8. Gurdon J. B., Wickens M. P. The use of Xenopus oocytes for the expression of cloned genes. Methods Enzymol. 1983;101:370–386. doi: 10.1016/0076-6879(83)01028-9. [DOI] [PubMed] [Google Scholar]
  9. Hediger M. A., Coady M. J., Ikeda T. S., Wright E. M. Expression cloning and cDNA sequencing of the Na+/glucose co-transporter. 1987 Nov 26-Dec 2Nature. 330(6146):379–381. doi: 10.1038/330379a0. [DOI] [PubMed] [Google Scholar]
  10. Hediger M. A., Ikeda T., Coady M., Gundersen C. B., Wright E. M. Expression of size-selected mRNA encoding the intestinal Na/glucose cotransporter in Xenopus laevis oocytes. Proc Natl Acad Sci U S A. 1987 May;84(9):2634–2637. doi: 10.1073/pnas.84.9.2634. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Horn A. S. Characteristics of neuronal dopamine uptake. Adv Biochem Psychopharmacol. 1978;19:25–34. [PubMed] [Google Scholar]
  12. Jacobson A. Purification and fractionation of poly(A)+ RNA. Methods Enzymol. 1987;152:254–261. doi: 10.1016/0076-6879(87)52028-6. [DOI] [PubMed] [Google Scholar]
  13. Johnston G. A., Lodge D., Bornstein J. C., Curtis D. R. Potentiation of L-glutamate and L-aspartate excitation of cat spinal neurones by the stereoisomers of threo-3-hydroxyaspartate. J Neurochem. 1980 Jan;34(1):241–243. doi: 10.1111/j.1471-4159.1980.tb04650.x. [DOI] [PubMed] [Google Scholar]
  14. Julius D., MacDermott A. B., Axel R., Jessell T. M. Molecular characterization of a functional cDNA encoding the serotonin 1c receptor. Science. 1988 Jul 29;241(4865):558–564. doi: 10.1126/science.3399891. [DOI] [PubMed] [Google Scholar]
  15. Kanner B. I. Bioenergetics of neurotransmitter transport. Biochim Biophys Acta. 1983 Dec 30;726(4):293–316. doi: 10.1016/0304-4173(83)90013-7. [DOI] [PubMed] [Google Scholar]
  16. Koepsell H. Methodological aspects of purification and reconstitution of transport proteins from mammalian plasma membranes. Rev Physiol Biochem Pharmacol. 1986;104:65–137. doi: 10.1007/BFb0031013. [DOI] [PubMed] [Google Scholar]
  17. Kusano K., Miledi R., Stinnakre J. Cholinergic and catecholaminergic receptors in the Xenopus oocyte membrane. J Physiol. 1982 Jul;328:143–170. doi: 10.1113/jphysiol.1982.sp014257. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Lodge D., Curtis D. R., Johnston G. A. Does uptake limit the actions of GABA agonists in vivo? Experiments with muscimol, isoguvacine and THIP in cat spinal cord. J Neurochem. 1978 Dec;31(6):1525–1528. doi: 10.1111/j.1471-4159.1978.tb06580.x. [DOI] [PubMed] [Google Scholar]
  19. Lübbert H., Hoffman B. J., Snutch T. P., van Dyke T., Levine A. J., Hartig P. R., Lester H. A., Davidson N. cDNA cloning of a serotonin 5-HT1C receptor by electrophysiological assays of mRNA-injected Xenopus oocytes. Proc Natl Acad Sci U S A. 1987 Jun;84(12):4332–4336. doi: 10.1073/pnas.84.12.4332. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. MacDonald R. J., Swift G. H., Przybyla A. E., Chirgwin J. M. Isolation of RNA using guanidinium salts. Methods Enzymol. 1987;152:219–227. doi: 10.1016/0076-6879(87)52023-7. [DOI] [PubMed] [Google Scholar]
  21. Masu Y., Nakayama K., Tamaki H., Harada Y., Kuno M., Nakanishi S. cDNA cloning of bovine substance-K receptor through oocyte expression system. 1987 Oct 29-Nov 4Nature. 329(6142):836–838. doi: 10.1038/329836a0. [DOI] [PubMed] [Google Scholar]
  22. Radian R., Bendahan A., Kanner B. I. Purification and identification of the functional sodium- and chloride-coupled gamma-aminobutyric acid transport glycoprotein from rat brain. J Biol Chem. 1986 Nov 25;261(33):15437–15441. [PubMed] [Google Scholar]
  23. Roberts P. J., Watkins J. C. Structural requirements for the inhibition for L-glutamate uptake by glia and nerve endings. Brain Res. 1975 Feb 21;85(1):120–125. doi: 10.1016/0006-8993(75)91016-1. [DOI] [PubMed] [Google Scholar]
  24. Ross S. B., Renyl A. L. Accumulation of tritiated 5-hydroxytryptamine in brain slices. Life Sci. 1967 Jul 1;6(13):1407–1415. doi: 10.1016/0024-3205(67)90188-9. [DOI] [PubMed] [Google Scholar]
  25. Sarthy V. gamma-Aminobutyric acid (GABA) uptake by Xenopus oocytes injected with rat brain mRNA. Brain Res. 1986 Jul;387(1):97–100. doi: 10.1016/0169-328x(86)90025-2. [DOI] [PubMed] [Google Scholar]
  26. Schousboe A. Transport and metabolism of glutamate and GABA in neurons are glial cells. Int Rev Neurobiol. 1981;22:1–45. doi: 10.1016/s0074-7742(08)60289-5. [DOI] [PubMed] [Google Scholar]
  27. Snutch T. P. The use of Xenopus oocytes to probe synaptic communication. Trends Neurosci. 1988 Jun;11(6):250–256. doi: 10.1016/0166-2236(88)90102-6. [DOI] [PubMed] [Google Scholar]
  28. Snyder S. H., Young A. B., Bennett J. P., Mulder A. H. Synaptic biochemistry of amino acids. Fed Proc. 1973 Oct;32(10):2039–2047. [PubMed] [Google Scholar]
  29. Steinbusch H. W. Distribution of serotonin-immunoreactivity in the central nervous system of the rat-cell bodies and terminals. Neuroscience. 1981;6(4):557–618. doi: 10.1016/0306-4522(81)90146-9. [DOI] [PubMed] [Google Scholar]
  30. Sumikawa K., Houghton M., Smith J. C., Bell L., Richards B. M., Barnard E. A. The molecular cloning and characterisation of cDNA coding for the alpha subunit of the acetylcholine receptor. Nucleic Acids Res. 1982 Oct 11;10(19):5809–5822. doi: 10.1093/nar/10.19.5809. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Ungerstedt U. Stereotaxic mapping of the monoamine pathways in the rat brain. Acta Physiol Scand Suppl. 1971;367:1–48. doi: 10.1111/j.1365-201x.1971.tb10998.x. [DOI] [PubMed] [Google Scholar]
  32. Wood J. D., Sidhu H. S. A comparative study and partial characterization of multi-uptake systems for gamma-aminobutyric acid. J Neurochem. 1987 Oct;49(4):1202–1208. doi: 10.1111/j.1471-4159.1987.tb10011.x. [DOI] [PubMed] [Google Scholar]
  33. Young A. B., Oster-Granite M. L., Herndon R. M., Snyder S. H. Glutamic acid: selective depletion by viral induced granule cell loss in hamster cerebellum. Brain Res. 1974 Jun 14;73(1):1–13. doi: 10.1016/0006-8993(74)91002-6. [DOI] [PubMed] [Google Scholar]

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