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The RNA-binding protein Adad1 is necessary for germ cell maintenance and meiosis in zebrafish

The double stranded RNA binding protein Adad1 (adenosine deaminase domain containing 1) is a member of the adenosine deaminase acting on RNAs (Adar) protein family with germ cell-specific expression. In mice, Adad1 is necessary for sperm differentiation, however its function outside of mammals has n...

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Autores principales: Islam, Kazi Nazrul, Ajao, Anuoluwapo, Venkataramani, Kavita, Rivera, Joshua, Pathania, Shailja, Henke, Katrin, Siegfried, Kellee Renee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10437952/
https://www.ncbi.nlm.nih.gov/pubmed/37552671
http://dx.doi.org/10.1371/journal.pgen.1010589
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author Islam, Kazi Nazrul
Ajao, Anuoluwapo
Venkataramani, Kavita
Rivera, Joshua
Pathania, Shailja
Henke, Katrin
Siegfried, Kellee Renee
author_facet Islam, Kazi Nazrul
Ajao, Anuoluwapo
Venkataramani, Kavita
Rivera, Joshua
Pathania, Shailja
Henke, Katrin
Siegfried, Kellee Renee
author_sort Islam, Kazi Nazrul
collection PubMed
description The double stranded RNA binding protein Adad1 (adenosine deaminase domain containing 1) is a member of the adenosine deaminase acting on RNAs (Adar) protein family with germ cell-specific expression. In mice, Adad1 is necessary for sperm differentiation, however its function outside of mammals has not been investigated. Here, through an N-ethyl-N-nitrosourea (ENU) based forward genetic screen, we identified an adad1 mutant zebrafish line that develops as sterile males. Further histological examination revealed complete lack of germ cells in adult mutant fish, however germ cells populated the gonad, proliferated, and entered meiosis in larval and juvenile fish. Although meiosis was initiated in adad1 mutant testes, the spermatocytes failed to progress beyond the zygotene stage. Thus, Adad1 is essential for meiosis and germline maintenance in zebrafish. We tested if spermatogonial stem cells were affected using nanos2 RNA FISH and a label retaining cell (LRC) assay, and found that the mutant testes had fewer LRCs and nanos2-expressing cells compared to wild-type siblings, suggesting that failure to maintain the spermatogonial stem cells resulted in germ cell loss by adulthood. To identify potential molecular processes regulated by Adad1, we sequenced bulk mRNA from mutants and wild-type testes and found mis-regulation of genes involved in RNA stability and modification, pointing to a potential broader role in post-transcriptional regulation. Our findings suggest that the RNA regulatory protein Adad1 is required for fertility through regulation of spermatogonial stem cell maintenance in zebrafish.
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spelling pubmed-104379522023-08-19 The RNA-binding protein Adad1 is necessary for germ cell maintenance and meiosis in zebrafish Islam, Kazi Nazrul Ajao, Anuoluwapo Venkataramani, Kavita Rivera, Joshua Pathania, Shailja Henke, Katrin Siegfried, Kellee Renee PLoS Genet Research Article The double stranded RNA binding protein Adad1 (adenosine deaminase domain containing 1) is a member of the adenosine deaminase acting on RNAs (Adar) protein family with germ cell-specific expression. In mice, Adad1 is necessary for sperm differentiation, however its function outside of mammals has not been investigated. Here, through an N-ethyl-N-nitrosourea (ENU) based forward genetic screen, we identified an adad1 mutant zebrafish line that develops as sterile males. Further histological examination revealed complete lack of germ cells in adult mutant fish, however germ cells populated the gonad, proliferated, and entered meiosis in larval and juvenile fish. Although meiosis was initiated in adad1 mutant testes, the spermatocytes failed to progress beyond the zygotene stage. Thus, Adad1 is essential for meiosis and germline maintenance in zebrafish. We tested if spermatogonial stem cells were affected using nanos2 RNA FISH and a label retaining cell (LRC) assay, and found that the mutant testes had fewer LRCs and nanos2-expressing cells compared to wild-type siblings, suggesting that failure to maintain the spermatogonial stem cells resulted in germ cell loss by adulthood. To identify potential molecular processes regulated by Adad1, we sequenced bulk mRNA from mutants and wild-type testes and found mis-regulation of genes involved in RNA stability and modification, pointing to a potential broader role in post-transcriptional regulation. Our findings suggest that the RNA regulatory protein Adad1 is required for fertility through regulation of spermatogonial stem cell maintenance in zebrafish. Public Library of Science 2023-08-08 /pmc/articles/PMC10437952/ /pubmed/37552671 http://dx.doi.org/10.1371/journal.pgen.1010589 Text en © 2023 Islam et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Islam, Kazi Nazrul
Ajao, Anuoluwapo
Venkataramani, Kavita
Rivera, Joshua
Pathania, Shailja
Henke, Katrin
Siegfried, Kellee Renee
The RNA-binding protein Adad1 is necessary for germ cell maintenance and meiosis in zebrafish
title The RNA-binding protein Adad1 is necessary for germ cell maintenance and meiosis in zebrafish
title_full The RNA-binding protein Adad1 is necessary for germ cell maintenance and meiosis in zebrafish
title_fullStr The RNA-binding protein Adad1 is necessary for germ cell maintenance and meiosis in zebrafish
title_full_unstemmed The RNA-binding protein Adad1 is necessary for germ cell maintenance and meiosis in zebrafish
title_short The RNA-binding protein Adad1 is necessary for germ cell maintenance and meiosis in zebrafish
title_sort rna-binding protein adad1 is necessary for germ cell maintenance and meiosis in zebrafish
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10437952/
https://www.ncbi.nlm.nih.gov/pubmed/37552671
http://dx.doi.org/10.1371/journal.pgen.1010589
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