TDP-43 regulates GAD1 mRNA splicing and GABA signaling in Drosophila CNS

Abstract Alterations in the function of the RNA-binding protein TDP-43 are largely associated with the pathogenesis of amyotrophic lateral sclerosis (ALS), a devastating disease of the human motor system that leads to motoneurons degeneration and reduced life expectancy by molecular mechanisms not w...

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Main Authors: Giulia Romano, Nikola Holodkov, Raffaella Klima, Fabian Feiguin
Format: Article
Language:English
Published: Nature Publishing Group 2021-09-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-98241-z
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spelling doaj-d38a7f08a17f4f109dbbf7984726cbf12021-09-26T11:28:18ZengNature Publishing GroupScientific Reports2045-23222021-09-011111810.1038/s41598-021-98241-zTDP-43 regulates GAD1 mRNA splicing and GABA signaling in Drosophila CNSGiulia Romano0Nikola Holodkov1Raffaella Klima2Fabian Feiguin3International Centre for Genetic Engineering and Biotechnology (ICGEB)International Centre for Genetic Engineering and Biotechnology (ICGEB)International Centre for Genetic Engineering and Biotechnology (ICGEB)International Centre for Genetic Engineering and Biotechnology (ICGEB)Abstract Alterations in the function of the RNA-binding protein TDP-43 are largely associated with the pathogenesis of amyotrophic lateral sclerosis (ALS), a devastating disease of the human motor system that leads to motoneurons degeneration and reduced life expectancy by molecular mechanisms not well known. In our previous work, we found that the expression levels of the glutamic acid decarboxylase enzyme (GAD1), responsible for converting glutamate to γ-aminobutyric acid (GABA), were downregulated in TBPH-null flies and motoneurons derived from ALS patients carrying mutations in TDP-43, suggesting that defects in the regulation of GAD1 may lead to neurodegeneration by affecting neurotransmitter balance. In this study, we observed that TBPH was required for the regulation of GAD1 pre-mRNA splicing and the levels of GABA in the Drosophila central nervous system (CNS). Interestingly, we discovered that pharmacological treatments aimed to potentiate GABA neurotransmission were able to revert locomotion deficiencies in TBPH-minus flies, revealing novel mechanisms and therapeutic strategies in ALS.https://doi.org/10.1038/s41598-021-98241-z
collection DOAJ
language English
format Article
sources DOAJ
author Giulia Romano
Nikola Holodkov
Raffaella Klima
Fabian Feiguin
spellingShingle Giulia Romano
Nikola Holodkov
Raffaella Klima
Fabian Feiguin
TDP-43 regulates GAD1 mRNA splicing and GABA signaling in Drosophila CNS
Scientific Reports
author_facet Giulia Romano
Nikola Holodkov
Raffaella Klima
Fabian Feiguin
author_sort Giulia Romano
title TDP-43 regulates GAD1 mRNA splicing and GABA signaling in Drosophila CNS
title_short TDP-43 regulates GAD1 mRNA splicing and GABA signaling in Drosophila CNS
title_full TDP-43 regulates GAD1 mRNA splicing and GABA signaling in Drosophila CNS
title_fullStr TDP-43 regulates GAD1 mRNA splicing and GABA signaling in Drosophila CNS
title_full_unstemmed TDP-43 regulates GAD1 mRNA splicing and GABA signaling in Drosophila CNS
title_sort tdp-43 regulates gad1 mrna splicing and gaba signaling in drosophila cns
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2021-09-01
description Abstract Alterations in the function of the RNA-binding protein TDP-43 are largely associated with the pathogenesis of amyotrophic lateral sclerosis (ALS), a devastating disease of the human motor system that leads to motoneurons degeneration and reduced life expectancy by molecular mechanisms not well known. In our previous work, we found that the expression levels of the glutamic acid decarboxylase enzyme (GAD1), responsible for converting glutamate to γ-aminobutyric acid (GABA), were downregulated in TBPH-null flies and motoneurons derived from ALS patients carrying mutations in TDP-43, suggesting that defects in the regulation of GAD1 may lead to neurodegeneration by affecting neurotransmitter balance. In this study, we observed that TBPH was required for the regulation of GAD1 pre-mRNA splicing and the levels of GABA in the Drosophila central nervous system (CNS). Interestingly, we discovered that pharmacological treatments aimed to potentiate GABA neurotransmission were able to revert locomotion deficiencies in TBPH-minus flies, revealing novel mechanisms and therapeutic strategies in ALS.
url https://doi.org/10.1038/s41598-021-98241-z
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