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Is d-aspartate produced by glutamic-oxaloacetic transaminase-1 like 1 (Got1l1): a putative aspartate racemase?

d-Aspartate is an endogenous free amino acid in the brain, endocrine tissues, and exocrine tissues in mammals, and it plays several physiological roles. In the testis, d-aspartate is detected in elongate spermatids, Leydig cells, and Sertoli cells, and implicated in the synthesis and release of test...

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Autores principales: Tanaka-Hayashi, Ayumi, Hayashi, Shuuhei, Inoue, Ran, Ito, Tomokazu, Konno, Kohtarou, Yoshida, Tomoyuki, Watanabe, Masahiko, Yoshimura, Tohru, Mori, Hisashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Vienna 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4282708/
https://www.ncbi.nlm.nih.gov/pubmed/25287256
http://dx.doi.org/10.1007/s00726-014-1847-3
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author Tanaka-Hayashi, Ayumi
Hayashi, Shuuhei
Inoue, Ran
Ito, Tomokazu
Konno, Kohtarou
Yoshida, Tomoyuki
Watanabe, Masahiko
Yoshimura, Tohru
Mori, Hisashi
author_facet Tanaka-Hayashi, Ayumi
Hayashi, Shuuhei
Inoue, Ran
Ito, Tomokazu
Konno, Kohtarou
Yoshida, Tomoyuki
Watanabe, Masahiko
Yoshimura, Tohru
Mori, Hisashi
author_sort Tanaka-Hayashi, Ayumi
collection PubMed
description d-Aspartate is an endogenous free amino acid in the brain, endocrine tissues, and exocrine tissues in mammals, and it plays several physiological roles. In the testis, d-aspartate is detected in elongate spermatids, Leydig cells, and Sertoli cells, and implicated in the synthesis and release of testosterone. In the hippocampus, d-aspartate strongly enhances N-methyl-d-aspartate receptor-dependent long-term potentiation and is involved in learning and memory. The existence of aspartate racemase, a candidate enzyme for d-aspartate production, has been suggested. Recently, mouse glutamic-oxaloacetic transaminase 1-like 1 (Got1l1) has been reported to synthesize substantially d-aspartate from l-aspartate and to be involved in adult neurogenesis. In this study, we investigated the function of Got1l1 in vivo by generating and analyzing Got1l1 knockout (KO) mice. We also examined the enzymatic activity of recombinant Got1l1 in vitro. We found that Got1l1 mRNA is highly expressed in the testis, but it is not detected in the brain and submandibular gland, where d-aspartate is abundant. The d-aspartate contents of wild-type and Got1l1 KO mice were not significantly different in the testis and hippocampus. The recombinant Got1l1 expressed in mammalian cells showed l-aspartate aminotransferase activity, but lacked aspartate racemase activity. These findings suggest that Got1l1 is not the major aspartate racemase and there might be an as yet unknown d-aspartate-synthesizing enzyme.
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spelling pubmed-42827082015-01-08 Is d-aspartate produced by glutamic-oxaloacetic transaminase-1 like 1 (Got1l1): a putative aspartate racemase? Tanaka-Hayashi, Ayumi Hayashi, Shuuhei Inoue, Ran Ito, Tomokazu Konno, Kohtarou Yoshida, Tomoyuki Watanabe, Masahiko Yoshimura, Tohru Mori, Hisashi Amino Acids Original Article d-Aspartate is an endogenous free amino acid in the brain, endocrine tissues, and exocrine tissues in mammals, and it plays several physiological roles. In the testis, d-aspartate is detected in elongate spermatids, Leydig cells, and Sertoli cells, and implicated in the synthesis and release of testosterone. In the hippocampus, d-aspartate strongly enhances N-methyl-d-aspartate receptor-dependent long-term potentiation and is involved in learning and memory. The existence of aspartate racemase, a candidate enzyme for d-aspartate production, has been suggested. Recently, mouse glutamic-oxaloacetic transaminase 1-like 1 (Got1l1) has been reported to synthesize substantially d-aspartate from l-aspartate and to be involved in adult neurogenesis. In this study, we investigated the function of Got1l1 in vivo by generating and analyzing Got1l1 knockout (KO) mice. We also examined the enzymatic activity of recombinant Got1l1 in vitro. We found that Got1l1 mRNA is highly expressed in the testis, but it is not detected in the brain and submandibular gland, where d-aspartate is abundant. The d-aspartate contents of wild-type and Got1l1 KO mice were not significantly different in the testis and hippocampus. The recombinant Got1l1 expressed in mammalian cells showed l-aspartate aminotransferase activity, but lacked aspartate racemase activity. These findings suggest that Got1l1 is not the major aspartate racemase and there might be an as yet unknown d-aspartate-synthesizing enzyme. Springer Vienna 2014-10-07 2015 /pmc/articles/PMC4282708/ /pubmed/25287256 http://dx.doi.org/10.1007/s00726-014-1847-3 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Article
Tanaka-Hayashi, Ayumi
Hayashi, Shuuhei
Inoue, Ran
Ito, Tomokazu
Konno, Kohtarou
Yoshida, Tomoyuki
Watanabe, Masahiko
Yoshimura, Tohru
Mori, Hisashi
Is d-aspartate produced by glutamic-oxaloacetic transaminase-1 like 1 (Got1l1): a putative aspartate racemase?
title Is d-aspartate produced by glutamic-oxaloacetic transaminase-1 like 1 (Got1l1): a putative aspartate racemase?
title_full Is d-aspartate produced by glutamic-oxaloacetic transaminase-1 like 1 (Got1l1): a putative aspartate racemase?
title_fullStr Is d-aspartate produced by glutamic-oxaloacetic transaminase-1 like 1 (Got1l1): a putative aspartate racemase?
title_full_unstemmed Is d-aspartate produced by glutamic-oxaloacetic transaminase-1 like 1 (Got1l1): a putative aspartate racemase?
title_short Is d-aspartate produced by glutamic-oxaloacetic transaminase-1 like 1 (Got1l1): a putative aspartate racemase?
title_sort is d-aspartate produced by glutamic-oxaloacetic transaminase-1 like 1 (got1l1): a putative aspartate racemase?
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4282708/
https://www.ncbi.nlm.nih.gov/pubmed/25287256
http://dx.doi.org/10.1007/s00726-014-1847-3
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