Literature DB >> 1697032

Expression of the neurotransmitter-synthesizing enzyme glutamic acid decarboxylase in male germ cells.

H Persson1, M Pelto-Huikko, M Metsis, O Söder, S Brene, S Skog, T Hökfelt, E M Ritzén.   

Abstract

The gene encoding glutamic acid decarboxylase (GAD), the key enzyme in the synthesis of the inhibitory neurotransmitter gamma-aminobutyric acid, is shown to be expressed in the testis of several different species. Nucleotide sequence analysis of a cDNA clone isolated from the human testis confirmed the presence of GAD mRNA in the testis. The major GAD mRNA in the testis was 2.5 kilobases. Smaller amounts of a 3.7-kilobase mRNA with the same size as GAD mRNA in the brain was also detected in the testis. In situ hybridization using a GAD-specific probe revealed GAD mRNA expressing spermatocytes and spermatids located in the middle part of rat seminiferous tubules. Studies on the ontogeny of GAD mRNA expression showed low levels of GAD mRNA in testes of prepubertal rats, with increasing levels as sexual maturation is reached, compatible with GAD mRNA expression in germ cells. In agreement with this, fractionation of cells from the rat seminiferous epithelium followed by Northern (RNA) blot analysis showed the highest levels of GAD mRNA associated with spermatocytes and spermatids. Evidence for the presence of GAD protein in the rat testis was obtained from the demonstration of GAD-like immunoreactivity in seminiferous tubules, predominantly at a position where spermatids and spermatozoa are found. Furthermore, GAD-like immunoreactivity was seen in the midpiece of ejaculated human spermatozoa, the part that is responsible for generating energy for spermatozoan motility.

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Year:  1990        PMID: 1697032      PMCID: PMC361065          DOI: 10.1128/mcb.10.9.4701-4711.1990

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  43 in total

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4.  Proopiomelanocortin cDNA sequences from the bovine ovary indicate alternative non-functional transcriptional initiation and a new polymorphism.

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Journal:  Nucleic Acids Res       Date:  1988-08-11       Impact factor: 16.971

5.  Purification and characterization of glutamate decarboxylase from mouse brain.

Authors:  J Y Wu; T Matsuda; E Roberts
Journal:  J Biol Chem       Date:  1973-05-10       Impact factor: 5.157

6.  Expression of the prodynorphin gene in male and female mammalian reproductive tissues.

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Journal:  Endocrinology       Date:  1987-02       Impact factor: 4.736

7.  Expression of proenkephalin messenger RNA by mouse spermatogenic cells.

Authors:  D L Kilpatrick; C F Millette
Journal:  Proc Natl Acad Sci U S A       Date:  1986-07       Impact factor: 11.205

8.  Developmental and regional expression of beta-nerve growth factor receptor mRNA in the chick and rat.

Authors:  P Ernfors; F Hallböök; T Ebendal; E M Shooter; M J Radeke; T P Misko; H Persson
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9.  The effects of opioid receptor antagonists suggest that testicular opiates regulate Sertoli and Leydig cell function in the neonatal rat.

Authors:  I Gerendai; C Shaha; G L Gunsalus; C W Bardin
Journal:  Endocrinology       Date:  1986-05       Impact factor: 4.736

10.  Newcastle disease virus-infected splenocytes express the proopiomelanocortin gene.

Authors:  H J Westly; A J Kleiss; K W Kelley; P K Wong; P H Yuen
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  16 in total

1.  Two distinct forms of the 64,000 Mr protein of the cleavage stimulation factor are expressed in mouse male germ cells.

Authors:  A M Wallace; B Dass; S E Ravnik; V Tonk; N A Jenkins; D J Gilbert; N G Copeland; C C MacDonald
Journal:  Proc Natl Acad Sci U S A       Date:  1999-06-08       Impact factor: 11.205

2.  New nucleotide sequence data on the EMBL File Server.

Authors: 
Journal:  Nucleic Acids Res       Date:  1991-05-11       Impact factor: 16.971

3.  Structure and alternative promoters of the mouse glutamic acid decarboxylase 67 gene.

Authors:  Y Yanagawa; T Kobayashi; T Kamei; K Ishii; M Nishijima; A Takaku; S Tamura
Journal:  Biochem J       Date:  1997-09-01       Impact factor: 3.857

4.  Association of GAD-65, but not of GAD-67, with the Golgi complex of transfected Chinese hamster ovary cells mediated by the N-terminal region.

Authors:  M Solimena; D Aggujaro; C Muntzel; R Dirkx; M Butler; P De Camilli; A Hayday
Journal:  Proc Natl Acad Sci U S A       Date:  1993-04-01       Impact factor: 11.205

Review 5.  GAD, diabetes, and Stiff-Man syndrome: some progress and more questions.

Authors:  M Solimena; M H Butler; P De Camilli
Journal:  J Endocrinol Invest       Date:  1994 Jul-Aug       Impact factor: 4.256

6.  Expression of multiple glutamate transporter splice variants in the rodent testis.

Authors:  Aven Lee; Ashley R Anderson; Amanda C Barnett; Anthony Chan; David V Pow
Journal:  Asian J Androl       Date:  2010-12-20       Impact factor: 3.285

7.  Demonstration of GAD-65 as the main immunogenic isoform of glutamate decarboxylase in type 1 diabetes and determination of autoantibodies using a radioligand produced by eukaryotic expression.

Authors:  L A Velloso; O Kämpe; A Hallberg; L Christmanson; C Betsholtz; F A Karlsson
Journal:  J Clin Invest       Date:  1993-05       Impact factor: 14.808

8.  Two human glutamate decarboxylases, 65-kDa GAD and 67-kDa GAD, are each encoded by a single gene.

Authors:  D F Bu; M G Erlander; B C Hitz; N J Tillakaratne; D L Kaufman; C B Wagner-McPherson; G A Evans; A J Tobin
Journal:  Proc Natl Acad Sci U S A       Date:  1992-03-15       Impact factor: 11.205

9.  Cloning, characterization, and autoimmune recognition of rat islet glutamic acid decarboxylase in insulin-dependent diabetes mellitus.

Authors:  B K Michelsen; J S Petersen; E Boel; A Møldrup; T Dyrberg; O D Madsen
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10.  Binding of antibodies in sera from Type 1 (insulin-dependent) diabetic patients to glutamate decarboxylase from rat tissues. Evidence for antigenic and non-antigenic forms of the enzyme.

Authors:  M R Christie; T J Brown; D Cassidy
Journal:  Diabetologia       Date:  1992-04       Impact factor: 10.122

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