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The Ntan1 gene is expressed in perineural glia and neurons of adult Drosophila
The Drosophila Ntan1 gene encodes an N-terminal asparagine amidohydrolase that we show is highly conserved throughout evolution. Protein isoforms share more than 72% of similarity with their human counterparts. At the cellular level, this gene regulates the type of glial cell growth in Drosophila la...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9427837/ https://www.ncbi.nlm.nih.gov/pubmed/36042338 http://dx.doi.org/10.1038/s41598-022-18999-8 |
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author | Castañeda-Sampedro, Ana Calvin-Cejudo, Laura Martin, Fernando Gomez-Diaz, Carolina Alcorta, Esther |
author_facet | Castañeda-Sampedro, Ana Calvin-Cejudo, Laura Martin, Fernando Gomez-Diaz, Carolina Alcorta, Esther |
author_sort | Castañeda-Sampedro, Ana |
collection | PubMed |
description | The Drosophila Ntan1 gene encodes an N-terminal asparagine amidohydrolase that we show is highly conserved throughout evolution. Protein isoforms share more than 72% of similarity with their human counterparts. At the cellular level, this gene regulates the type of glial cell growth in Drosophila larvae by its different expression levels. The Drosophila Ntan1 gene has 4 transcripts that encode 2 protein isoforms. Here we describe that although this gene is expressed at all developmental stages and adult organs tested (eye, antennae and brain) there are some transcript-dependent specificities. Therefore, both quantitative and qualitative cues could account for gene function. However, widespread developmental stage and organ-dependent expression could be masking cell-specific constraints that can be explored in Drosophila by using Gal4 drivers. We report a new genetic driver within this gene, Mz317-Gal4, that recapitulates the Ntan1 gene expression pattern in adults. It shows specific expression for perineural glia in the olfactory organs but mixed expression with some neurons in the adult brain. Memory and social behavior disturbances in mice and cancer and schizophrenia in humans have been linked to the Ntan1 gene. Therefore, these new tools in Drosophila may contribute to our understanding of the cellular basis of these alterations. |
format | Online Article Text |
id | pubmed-9427837 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-94278372022-09-01 The Ntan1 gene is expressed in perineural glia and neurons of adult Drosophila Castañeda-Sampedro, Ana Calvin-Cejudo, Laura Martin, Fernando Gomez-Diaz, Carolina Alcorta, Esther Sci Rep Article The Drosophila Ntan1 gene encodes an N-terminal asparagine amidohydrolase that we show is highly conserved throughout evolution. Protein isoforms share more than 72% of similarity with their human counterparts. At the cellular level, this gene regulates the type of glial cell growth in Drosophila larvae by its different expression levels. The Drosophila Ntan1 gene has 4 transcripts that encode 2 protein isoforms. Here we describe that although this gene is expressed at all developmental stages and adult organs tested (eye, antennae and brain) there are some transcript-dependent specificities. Therefore, both quantitative and qualitative cues could account for gene function. However, widespread developmental stage and organ-dependent expression could be masking cell-specific constraints that can be explored in Drosophila by using Gal4 drivers. We report a new genetic driver within this gene, Mz317-Gal4, that recapitulates the Ntan1 gene expression pattern in adults. It shows specific expression for perineural glia in the olfactory organs but mixed expression with some neurons in the adult brain. Memory and social behavior disturbances in mice and cancer and schizophrenia in humans have been linked to the Ntan1 gene. Therefore, these new tools in Drosophila may contribute to our understanding of the cellular basis of these alterations. Nature Publishing Group UK 2022-08-30 /pmc/articles/PMC9427837/ /pubmed/36042338 http://dx.doi.org/10.1038/s41598-022-18999-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Castañeda-Sampedro, Ana Calvin-Cejudo, Laura Martin, Fernando Gomez-Diaz, Carolina Alcorta, Esther The Ntan1 gene is expressed in perineural glia and neurons of adult Drosophila |
title | The Ntan1 gene is expressed in perineural glia and neurons of adult Drosophila |
title_full | The Ntan1 gene is expressed in perineural glia and neurons of adult Drosophila |
title_fullStr | The Ntan1 gene is expressed in perineural glia and neurons of adult Drosophila |
title_full_unstemmed | The Ntan1 gene is expressed in perineural glia and neurons of adult Drosophila |
title_short | The Ntan1 gene is expressed in perineural glia and neurons of adult Drosophila |
title_sort | ntan1 gene is expressed in perineural glia and neurons of adult drosophila |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9427837/ https://www.ncbi.nlm.nih.gov/pubmed/36042338 http://dx.doi.org/10.1038/s41598-022-18999-8 |
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