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Distinct Roles of NANOS1 and NANOS3 in the Cell Cycle and NANOS3-PUM1-FOXM1 Axis to Control G2/M Phase in a Human Primordial Germ Cell Model

Nanos RNA-binding proteins are critical factors of germline development throughout the animal kingdom and their dysfunction causes infertility. During evolution, mammalian Nanos paralogues adopted divergent roles in germ cell biology. However, the molecular basis behind this divergence, such as thei...

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Autores principales: Ilaslan, Erkut, Kwiatkowska, Krystyna, Smialek, Maciej Jerzy, Sajek, Marcin Piotr, Lemanska, Zaneta, Alla, Matisa, Janecki, Damian Mikolaj, Jaruzelska, Jadwiga, Kusz-Zamelczyk, Kamila
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9223905/
https://www.ncbi.nlm.nih.gov/pubmed/35743036
http://dx.doi.org/10.3390/ijms23126592
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author Ilaslan, Erkut
Kwiatkowska, Krystyna
Smialek, Maciej Jerzy
Sajek, Marcin Piotr
Lemanska, Zaneta
Alla, Matisa
Janecki, Damian Mikolaj
Jaruzelska, Jadwiga
Kusz-Zamelczyk, Kamila
author_facet Ilaslan, Erkut
Kwiatkowska, Krystyna
Smialek, Maciej Jerzy
Sajek, Marcin Piotr
Lemanska, Zaneta
Alla, Matisa
Janecki, Damian Mikolaj
Jaruzelska, Jadwiga
Kusz-Zamelczyk, Kamila
author_sort Ilaslan, Erkut
collection PubMed
description Nanos RNA-binding proteins are critical factors of germline development throughout the animal kingdom and their dysfunction causes infertility. During evolution, mammalian Nanos paralogues adopted divergent roles in germ cell biology. However, the molecular basis behind this divergence, such as their target mRNAs, remains poorly understood. Our RNA-sequencing analysis in a human primordial germ cell model-TCam-2 cell line revealed distinct pools of genes involved in the cell cycle process downregulated upon NANOS1 and NANOS3 overexpression. We show that NANOS1 and NANOS3 proteins influence different stages of the cell cycle. Namely, NANOS1 is involved in the G1/S and NANOS3 in the G2/M phase transition. Many of their cell cycle targets are known infertility and cancer-germ cell genes. Moreover, NANOS3 in complex with RNA-binding protein PUM1 causes 3′UTR-mediated repression of FOXM1 mRNA encoding a transcription factor crucial for G2/M phase transition. Interestingly, while NANOS3 and PUM1 act as post-transcriptional repressors of FOXM1, FOXM1 potentially acts as a transcriptional activator of NANOS3, PUM1, and itself. Finally, by utilizing publicly available RNA-sequencing datasets, we show that the balance between FOXM1-NANOS3 and FOXM1-PUM1 expression levels is disrupted in testis cancer, suggesting a potential role in this disease.
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spelling pubmed-92239052022-06-24 Distinct Roles of NANOS1 and NANOS3 in the Cell Cycle and NANOS3-PUM1-FOXM1 Axis to Control G2/M Phase in a Human Primordial Germ Cell Model Ilaslan, Erkut Kwiatkowska, Krystyna Smialek, Maciej Jerzy Sajek, Marcin Piotr Lemanska, Zaneta Alla, Matisa Janecki, Damian Mikolaj Jaruzelska, Jadwiga Kusz-Zamelczyk, Kamila Int J Mol Sci Article Nanos RNA-binding proteins are critical factors of germline development throughout the animal kingdom and their dysfunction causes infertility. During evolution, mammalian Nanos paralogues adopted divergent roles in germ cell biology. However, the molecular basis behind this divergence, such as their target mRNAs, remains poorly understood. Our RNA-sequencing analysis in a human primordial germ cell model-TCam-2 cell line revealed distinct pools of genes involved in the cell cycle process downregulated upon NANOS1 and NANOS3 overexpression. We show that NANOS1 and NANOS3 proteins influence different stages of the cell cycle. Namely, NANOS1 is involved in the G1/S and NANOS3 in the G2/M phase transition. Many of their cell cycle targets are known infertility and cancer-germ cell genes. Moreover, NANOS3 in complex with RNA-binding protein PUM1 causes 3′UTR-mediated repression of FOXM1 mRNA encoding a transcription factor crucial for G2/M phase transition. Interestingly, while NANOS3 and PUM1 act as post-transcriptional repressors of FOXM1, FOXM1 potentially acts as a transcriptional activator of NANOS3, PUM1, and itself. Finally, by utilizing publicly available RNA-sequencing datasets, we show that the balance between FOXM1-NANOS3 and FOXM1-PUM1 expression levels is disrupted in testis cancer, suggesting a potential role in this disease. MDPI 2022-06-13 /pmc/articles/PMC9223905/ /pubmed/35743036 http://dx.doi.org/10.3390/ijms23126592 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ilaslan, Erkut
Kwiatkowska, Krystyna
Smialek, Maciej Jerzy
Sajek, Marcin Piotr
Lemanska, Zaneta
Alla, Matisa
Janecki, Damian Mikolaj
Jaruzelska, Jadwiga
Kusz-Zamelczyk, Kamila
Distinct Roles of NANOS1 and NANOS3 in the Cell Cycle and NANOS3-PUM1-FOXM1 Axis to Control G2/M Phase in a Human Primordial Germ Cell Model
title Distinct Roles of NANOS1 and NANOS3 in the Cell Cycle and NANOS3-PUM1-FOXM1 Axis to Control G2/M Phase in a Human Primordial Germ Cell Model
title_full Distinct Roles of NANOS1 and NANOS3 in the Cell Cycle and NANOS3-PUM1-FOXM1 Axis to Control G2/M Phase in a Human Primordial Germ Cell Model
title_fullStr Distinct Roles of NANOS1 and NANOS3 in the Cell Cycle and NANOS3-PUM1-FOXM1 Axis to Control G2/M Phase in a Human Primordial Germ Cell Model
title_full_unstemmed Distinct Roles of NANOS1 and NANOS3 in the Cell Cycle and NANOS3-PUM1-FOXM1 Axis to Control G2/M Phase in a Human Primordial Germ Cell Model
title_short Distinct Roles of NANOS1 and NANOS3 in the Cell Cycle and NANOS3-PUM1-FOXM1 Axis to Control G2/M Phase in a Human Primordial Germ Cell Model
title_sort distinct roles of nanos1 and nanos3 in the cell cycle and nanos3-pum1-foxm1 axis to control g2/m phase in a human primordial germ cell model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9223905/
https://www.ncbi.nlm.nih.gov/pubmed/35743036
http://dx.doi.org/10.3390/ijms23126592
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