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PACT/PRKRA and p53 regulate transcriptional activity of DMRT1
The transcription factor DMRT1 (doublesex and mab-3 related transcription factor) has two distinct functions, somatic-cell masculinization and germ-cell development in some vertebrate species, including mouse and the African clawed frog Xenopus laevis. However, its transcriptional regulation remains...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Genética
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7198010/ https://www.ncbi.nlm.nih.gov/pubmed/32251494 http://dx.doi.org/10.1590/1678-4685-GMB-2019-0017 |
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author | Fujitani, Kazuko Otomo, Asako Nagayama, Yuto Tachibana, Taro Kato, Rika Kawashima, Yusuke Kodera, Yoshio Kato, Tomoko Takada, Shuji Tamura, Kei Takamatsu, Nobuhiko Ito, Michihiko |
author_facet | Fujitani, Kazuko Otomo, Asako Nagayama, Yuto Tachibana, Taro Kato, Rika Kawashima, Yusuke Kodera, Yoshio Kato, Tomoko Takada, Shuji Tamura, Kei Takamatsu, Nobuhiko Ito, Michihiko |
author_sort | Fujitani, Kazuko |
collection | PubMed |
description | The transcription factor DMRT1 (doublesex and mab-3 related transcription factor) has two distinct functions, somatic-cell masculinization and germ-cell development in some vertebrate species, including mouse and the African clawed frog Xenopus laevis. However, its transcriptional regulation remains unclear. We tried to identify DMRT1-interacting proteins from X. laevis testes by immunoprecipitation with an anti-DMRT1 antibody and MS/MS analysis, and selected three proteins, including PACT/PRKRA (Interferon-inducible double-stranded RNA dependent protein kinase activator A) derived from testes. Next, we examined the effects of PACT/PRKRA and/or p53 on the transcriptional activity of DMRT1. In transfected 293T cells, PACT/PRKRA and p53 significantly enhanced and repressed DMRT1-driven luciferase activity, respectively. We also observed that the enhanced activity by PACT/PRKRA was strongly attenuated by p53. Moreover, in situ hybridization analysis of Pact/Prkra mRNA in tadpole gonads indicated high expression in female and male germline stem cells. Taken together, these findings suggest that PACT/PRKRA and p53 might positively and negatively regulate the activity of DMRT1, respectively, for germline stem cell fate. |
format | Online Article Text |
id | pubmed-7198010 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Sociedade Brasileira de Genética |
record_format | MEDLINE/PubMed |
spelling | pubmed-71980102020-05-08 PACT/PRKRA and p53 regulate transcriptional activity of DMRT1 Fujitani, Kazuko Otomo, Asako Nagayama, Yuto Tachibana, Taro Kato, Rika Kawashima, Yusuke Kodera, Yoshio Kato, Tomoko Takada, Shuji Tamura, Kei Takamatsu, Nobuhiko Ito, Michihiko Genet Mol Biol Cellular, Molecular and Developmental Genetics The transcription factor DMRT1 (doublesex and mab-3 related transcription factor) has two distinct functions, somatic-cell masculinization and germ-cell development in some vertebrate species, including mouse and the African clawed frog Xenopus laevis. However, its transcriptional regulation remains unclear. We tried to identify DMRT1-interacting proteins from X. laevis testes by immunoprecipitation with an anti-DMRT1 antibody and MS/MS analysis, and selected three proteins, including PACT/PRKRA (Interferon-inducible double-stranded RNA dependent protein kinase activator A) derived from testes. Next, we examined the effects of PACT/PRKRA and/or p53 on the transcriptional activity of DMRT1. In transfected 293T cells, PACT/PRKRA and p53 significantly enhanced and repressed DMRT1-driven luciferase activity, respectively. We also observed that the enhanced activity by PACT/PRKRA was strongly attenuated by p53. Moreover, in situ hybridization analysis of Pact/Prkra mRNA in tadpole gonads indicated high expression in female and male germline stem cells. Taken together, these findings suggest that PACT/PRKRA and p53 might positively and negatively regulate the activity of DMRT1, respectively, for germline stem cell fate. Sociedade Brasileira de Genética 2020-03-30 /pmc/articles/PMC7198010/ /pubmed/32251494 http://dx.doi.org/10.1590/1678-4685-GMB-2019-0017 Text en Copyright © 2020, Sociedade Brasileira de Genética. https://creativecommons.org/licenses/by/4.0/ License information: This is an open-access article distributed under the terms of the Creative Commons Attribution License (type CC-BY), which permits unrestricted use, distribution and reproduction in any medium, provided the original article is properly cited. |
spellingShingle | Cellular, Molecular and Developmental Genetics Fujitani, Kazuko Otomo, Asako Nagayama, Yuto Tachibana, Taro Kato, Rika Kawashima, Yusuke Kodera, Yoshio Kato, Tomoko Takada, Shuji Tamura, Kei Takamatsu, Nobuhiko Ito, Michihiko PACT/PRKRA and p53 regulate transcriptional activity of DMRT1 |
title | PACT/PRKRA and p53 regulate transcriptional activity of
DMRT1 |
title_full | PACT/PRKRA and p53 regulate transcriptional activity of
DMRT1 |
title_fullStr | PACT/PRKRA and p53 regulate transcriptional activity of
DMRT1 |
title_full_unstemmed | PACT/PRKRA and p53 regulate transcriptional activity of
DMRT1 |
title_short | PACT/PRKRA and p53 regulate transcriptional activity of
DMRT1 |
title_sort | pact/prkra and p53 regulate transcriptional activity of
dmrt1 |
topic | Cellular, Molecular and Developmental Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7198010/ https://www.ncbi.nlm.nih.gov/pubmed/32251494 http://dx.doi.org/10.1590/1678-4685-GMB-2019-0017 |
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