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Tytuł pozycji:

Long reach of the NAAG family tree: An Editorial for "Evidence of NAAG-family tripeptide NAAG2 in the Drosophila nervous system" on page 38.

Tytuł :
Long reach of the NAAG family tree: An Editorial for "Evidence of NAAG-family tripeptide NAAG2 in the Drosophila nervous system" on page 38.
Autorzy :
Williams S; Imaging Science and Biomedical Engineering, University of Manchester, Manchester, UK.
Rae CD; NeuRA Imaging, Neuroscience Research Australia, Randwick, NSW, Australia.
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Źródło :
Journal of neurochemistry [J Neurochem] 2021 Jan; Vol. 156 (1), pp. 13-15. Date of Electronic Publication: 2020 Nov 16.
Typ publikacji :
Editorial; Comment
Język :
English
Imprint Name(s) :
Publication: 2001- : Oxford, UK : Wiley on behalf of the International Society for Neurochemistry
Original Publication: New York : Raven Press
MeSH Terms :
Aspartic Acid*
Drosophila*
Animals ; Dipeptides ; Drosophila melanogaster ; Nervous System ; Pedigree
References :
Amherd, R., Hintermann, E., Walz, D., Affolter, M., & Meyer, U. A. (2000). Purification, cloning, and characterization of a second arylalkylamine N-acetyltransferase from Drosophila melanogaster. DNA and Cell Biology, 19, 697-705.
Becker, I., Lodder, J., Gieselmann, V., & Eckhardt, M. (2010). Molecular characterization of N-acetylaspartylglutamate synthetase. Journal of Biological Chemistry, 285, 29156-29164.
Buschbeck, E. K., & Friedrich, M. (2008). Evolution of insect eyes: Tales of ancient heritage, deconstruction. Reconstruction, Remodeling, and Recycling. Evolution: Education and Outreach, 1, 448-462.
Collard, F., Stroobant, V., Lamosa, P., Kapanda, C. N., Lambert, D. M., Muccioli, G. G., Poupaert, J. H., Opperdoes, F., & Van Schaftingen, E. (2010). Molecular identification of N-acetylaspartylglutamate synthase and β-citrylglutamate synthase. Journal of Biological Chemistry, 285, 29826-29833.
Hintermann, E., Grieder, N. C., Amherd, R., Brodbeck, D., & Meyer, U. A. (1996). Cloning of an arylalkylamine N-acetyltransferase (aaNAT1) from Drosophila melanogaster expressed in the nervous system and the gut. Proceedings of the National Academy of Sciences, 93, 12315. https://doi.org/10.1073/pnas.93.22.12315.
Johnson, E. C. (2011). N-Acetylaspartylglutamate is not demonstrated to be a selective mGlu3 receptor agonist. Journal of Neurochemistry, 119, 896-898.
Kozik, E. M., Marzluff, E. M., & Lindgren, C. A. (2020). Evidence of NAAG-family tripeptide NAAG2 in the Drosophila Nervous System. Journal of Neurochemistry, n/a.
Lodder-Gadaczek, J., Becker, I., Gieselmann, V., Wang-Eckhardt, L., & Eckhardt, M. (2011). N-acetylaspartylglutamate synthetase II synthesizes N-acetylaspartylglutamylglutamate. Journal of Biological Chemistry, 286, 16693-16706.
Lodder-Gadaczek, J., Gieselmann, V., & Eckhardt, M. (2013). Vesicular uptake of N-acetylaspartylglutamate is catalysed by sialin (SLC17A5). The Biochemical Journal, 454, 31-38.
Neale, J. H. (2011). N-Acetylaspartylglutamate is an agonist at mGluR3 in vivo and in vitro. Journal of Neurochemistry, 119, 891-895.
Neale, J. H., Olszewski, R. T., Zuo, D., Janczura, K. J., Profaci, C. P., Lavin, K. M., Madore, J. C., & Bzdega, T. (2011). Advances in understanding the peptide neurotransmitter NAAG and appearance of a new member of the NAAG neuropeptide family. Journal of Neurochemistry, 118, 490-498.
Olszewski, R. T., Janczura, K. J., Bzdega, T., Der, E. K., Venzor, F., O’Rourke, B., Hark, T. J., Craddock, K. E., Balasubramanian, S., Moussa, C., & Neale, J. H. (2017). NAAG peptidase inhibitors act via mGluR3: Animal models of memory, Alzheimer’s, and ethanol intoxication. Neurochemical Research, 42, 2646-2657. https://doi.org/10.1007/s11064-017-2181-4.
Reichelt, K., & Kvamme, E. (1973). Histamine-dependent formation of N-acetyl-aspartyl peptides in mouse brain. Journal of Neurochemistry, 21, 849-859.
Urazaev, A. K., Grossfeld, R., Fletcher, P., Speno, H., Gafurov, B. S., Buttram, J., & Lieberman, E. (2001). Synthesis and release of N-acetylaspartylglutamate (NAAG) by crayfish nerve fibers: Implications for axon-glia signaling. Neuroscience, 106, 237-247. https://doi.org/10.1016/S0306-4522(01)00270-6.
Wilinski, D., Winzeler, J., Duren, W., Persons, J. L., Holme, K. J., Mosquera, J., Khabiri, M., Kinchen, J. M., Freddolino, P. L., Karnovsky, A., & Dus, M. (2019). Rapid metabolic shifts occur during the transition between hunger and satiety in Drosophila melanogaster. Nature Communications, 10, 4052. https://doi.org/10.1038/s41467-019-11933-z.
Zhang, Q., Lu, Y. -X., & Xu, W. -H. (2012). Integrated proteomic and metabolomic analysis of larval brain associated with diapause induction and preparation in the cotton bollworm. Helicoverpa Armigera. Journal of Proteome Research, 11, 1042-1053.
Substance Nomenclature :
0 (Dipeptides)
1W8M12WXYL (isospaglumic acid)
30KYC7MIAI (Aspartic Acid)
Entry Date(s) :
Date Created: 20201116 Date Completed: 20210413 Latest Revision: 20210413
Update Code :
20210414
DOI :
10.1111/jnc.15213
PMID :
33197055
Opinia redakcyjna
The last common ancestor of humans and fruit flies lived about 800 million years ago, yet both of us have nervous systems that share a number of common important features, for example the use of glutamate as a neurotransmitter. We can now possibly add another common feature to the neural tissue of humans and fruit flies which is that of N-acetylaspartylglutamate (NAAG) peptides. This Editorial highlights an article by Kozik and coworkers in the current issue of the Journal of Neurochemistry, in which the authors report the discovery, in Drosophila melanogaster nervous system, of NAA-glutamylglutamate (NAAG2).
(© 2020 International Society for Neurochemistry.)
Comment on: J Neurochem. 2021 Jan;156(1):38-47. (PMID: 32885844)

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