PACT/PRKRA and p53 regulate transcriptional activity of DMRT1

Abstract 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 regulatio...

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Main Authors: Kazuko Fujitani, Asako Otomo, Yuto Nagayama, Taro Tachibana, Rika Kato, Yusuke Kawashima, Yoshio Kodera, Tomoko Kato, Shuji Takada, Kei Tamura, Nobuhiko Takamatsu, Michihiko Ito
Format: Article
Language:English
Published: Sociedade Brasileira de Genética 2020-03-01
Series:Genetics and Molecular Biology
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Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572020000400702&tlng=en
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author Kazuko Fujitani
Asako Otomo
Yuto Nagayama
Taro Tachibana
Rika Kato
Yusuke Kawashima
Yoshio Kodera
Tomoko Kato
Shuji Takada
Kei Tamura
Nobuhiko Takamatsu
Michihiko Ito
author_facet Kazuko Fujitani
Asako Otomo
Yuto Nagayama
Taro Tachibana
Rika Kato
Yusuke Kawashima
Yoshio Kodera
Tomoko Kato
Shuji Takada
Kei Tamura
Nobuhiko Takamatsu
Michihiko Ito
author_sort Kazuko Fujitani
collection DOAJ
description Abstract 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.
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spelling doaj.art-501a9209faca4a77a18987add58d33032022-12-21T19:29:06ZengSociedade Brasileira de GenéticaGenetics and Molecular Biology1678-46852020-03-0143210.1590/1678-4685-gmb-2019-0017PACT/PRKRA and p53 regulate transcriptional activity of DMRT1Kazuko FujitaniAsako OtomoYuto NagayamaTaro TachibanaRika KatoYusuke KawashimaYoshio KoderaTomoko KatoShuji TakadaKei TamuraNobuhiko TakamatsuMichihiko Itohttps://orcid.org/0000-0003-1881-6916Abstract 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.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572020000400702&tlng=enp53DMRT1germline stem celltestisXenopus
spellingShingle Kazuko Fujitani
Asako Otomo
Yuto Nagayama
Taro Tachibana
Rika Kato
Yusuke Kawashima
Yoshio Kodera
Tomoko Kato
Shuji Takada
Kei Tamura
Nobuhiko Takamatsu
Michihiko Ito
PACT/PRKRA and p53 regulate transcriptional activity of DMRT1
Genetics and Molecular Biology
p53
DMRT1
germline stem cell
testis
Xenopus
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 p53
DMRT1
germline stem cell
testis
Xenopus
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572020000400702&tlng=en
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