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Meiotic gatekeeper STRA8 regulates cell cycle by interacting with SETD8 during spermatogenesis

STRA8 (Stimulated By Retinoic Acid Gene 8) is a retinoic acid (RA) induced gene that plays vital roles in spermatogonial proliferation, differentiation and meiosis. The SETD8 and STRA8 protein interaction was discovered using the yeast two‐hybrid technique using a mouse spermatogonial stem cell (SSC...

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Autores principales: Niu, Changmin, Guo, Jiaqian, Shen, Xueyi, Ma, Shikun, Xia, Mengmeng, Xia, Jing, Zheng, Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7171306/
https://www.ncbi.nlm.nih.gov/pubmed/32090428
http://dx.doi.org/10.1111/jcmm.15080
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author Niu, Changmin
Guo, Jiaqian
Shen, Xueyi
Ma, Shikun
Xia, Mengmeng
Xia, Jing
Zheng, Ying
author_facet Niu, Changmin
Guo, Jiaqian
Shen, Xueyi
Ma, Shikun
Xia, Mengmeng
Xia, Jing
Zheng, Ying
author_sort Niu, Changmin
collection PubMed
description STRA8 (Stimulated By Retinoic Acid Gene 8) is a retinoic acid (RA) induced gene that plays vital roles in spermatogonial proliferation, differentiation and meiosis. The SETD8 and STRA8 protein interaction was discovered using the yeast two‐hybrid technique using a mouse spermatogonial stem cell (SSC) cDNA library. The interaction of these two proteins was confirmed using co‐immunoprecipitation and identification of key domains governing the protein: protein complex. STRA8 and SETD8 showed a mutual transcriptional regulation pattern that provided evidence that SETD8 negatively regulated transcriptional activity of the STRA8 promoter. The SETD8 protein directly bound to the proximal promoter of the STRA8 gene. STRA8 increased the transcriptional activity of SETD8 promoter in a dose‐dependent manner. For the first time, we have discovered that STRA8 and SETD8 display a cell cycle‐dependent expression pattern in germline cells. Expression levels of SETD8 and H4K20me1 in S phase of STRA8 overexpression GC1 cells were different from that previously observed in tumour cell lines. In wild‐type mice testis, SETD8, H4K20me1 and PCNA co‐localized with STRA8 in spermatogonia. Further, our studies quantitated abnormal expression levels of cell cycle and ubiquitination‐related factors in STRA8 dynamic models. STRA8 and SETD8 may regulate spermatogenesis via Cdl4‐Clu4A‐Ddb1 ubiquitinated degradation axis in a PCNA‐dependent manner.
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spelling pubmed-71713062020-04-21 Meiotic gatekeeper STRA8 regulates cell cycle by interacting with SETD8 during spermatogenesis Niu, Changmin Guo, Jiaqian Shen, Xueyi Ma, Shikun Xia, Mengmeng Xia, Jing Zheng, Ying J Cell Mol Med Original Articles STRA8 (Stimulated By Retinoic Acid Gene 8) is a retinoic acid (RA) induced gene that plays vital roles in spermatogonial proliferation, differentiation and meiosis. The SETD8 and STRA8 protein interaction was discovered using the yeast two‐hybrid technique using a mouse spermatogonial stem cell (SSC) cDNA library. The interaction of these two proteins was confirmed using co‐immunoprecipitation and identification of key domains governing the protein: protein complex. STRA8 and SETD8 showed a mutual transcriptional regulation pattern that provided evidence that SETD8 negatively regulated transcriptional activity of the STRA8 promoter. The SETD8 protein directly bound to the proximal promoter of the STRA8 gene. STRA8 increased the transcriptional activity of SETD8 promoter in a dose‐dependent manner. For the first time, we have discovered that STRA8 and SETD8 display a cell cycle‐dependent expression pattern in germline cells. Expression levels of SETD8 and H4K20me1 in S phase of STRA8 overexpression GC1 cells were different from that previously observed in tumour cell lines. In wild‐type mice testis, SETD8, H4K20me1 and PCNA co‐localized with STRA8 in spermatogonia. Further, our studies quantitated abnormal expression levels of cell cycle and ubiquitination‐related factors in STRA8 dynamic models. STRA8 and SETD8 may regulate spermatogenesis via Cdl4‐Clu4A‐Ddb1 ubiquitinated degradation axis in a PCNA‐dependent manner. John Wiley and Sons Inc. 2020-02-24 2020-04 /pmc/articles/PMC7171306/ /pubmed/32090428 http://dx.doi.org/10.1111/jcmm.15080 Text en © 2020 School of Medicine, Yangzhou University. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Niu, Changmin
Guo, Jiaqian
Shen, Xueyi
Ma, Shikun
Xia, Mengmeng
Xia, Jing
Zheng, Ying
Meiotic gatekeeper STRA8 regulates cell cycle by interacting with SETD8 during spermatogenesis
title Meiotic gatekeeper STRA8 regulates cell cycle by interacting with SETD8 during spermatogenesis
title_full Meiotic gatekeeper STRA8 regulates cell cycle by interacting with SETD8 during spermatogenesis
title_fullStr Meiotic gatekeeper STRA8 regulates cell cycle by interacting with SETD8 during spermatogenesis
title_full_unstemmed Meiotic gatekeeper STRA8 regulates cell cycle by interacting with SETD8 during spermatogenesis
title_short Meiotic gatekeeper STRA8 regulates cell cycle by interacting with SETD8 during spermatogenesis
title_sort meiotic gatekeeper stra8 regulates cell cycle by interacting with setd8 during spermatogenesis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7171306/
https://www.ncbi.nlm.nih.gov/pubmed/32090428
http://dx.doi.org/10.1111/jcmm.15080
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