STAT3 Is an Upstream Regulator of <i>Granzyme G</i> in the Maternal-To-Zygotic Transition of Mouse Embryos

The maternal-to-zygotic transition (MZT), which controls maternal signaling to synthesize zygotic gene products, promotes the preimplantation development of mouse zygotes to the two-cell stage. Our previous study reported that mouse granzyme g (Gzmg), a serine-type protease, is required for the MZT....

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Main Authors: Huan Ou-Yang, Shinn-Chih Wu, Li-Ying Sung, Shiao-Hsuan Yang, Shang-Hsun Yang, Kowit-Yu Chong, Chuan-Mu Chen
Format: Article
Language:English
Published: MDPI AG 2021-01-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/22/1/460
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spelling doaj-0d10d2d6c15743fc90cdf31412571ace2021-01-06T00:03:28ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672021-01-012246046010.3390/ijms22010460STAT3 Is an Upstream Regulator of <i>Granzyme G</i> in the Maternal-To-Zygotic Transition of Mouse EmbryosHuan Ou-Yang0Shinn-Chih Wu1Li-Ying Sung2Shiao-Hsuan Yang3Shang-Hsun Yang4Kowit-Yu Chong5Chuan-Mu Chen6Department of Life Sciences, and Ph.D. Program in Translational Medicine, National Chung Hsing University, Taichung 402, TaiwanDepartment of Animal Science and Technology, National Taiwan University, Taipei 106, TaiwanInstitute of Biotechnology, National Taiwan University, Taipei 106, TaiwanDepartment of Life Sciences, and Ph.D. Program in Translational Medicine, National Chung Hsing University, Taichung 402, TaiwanDepartment of Physiology, National Cheng Kung University, Tainan 70101, TaiwanDepartment of Medical Biotechnology and Laboratory Science, College of Medicine, Chang Gung University, Taoyuan 333, TaiwanDepartment of Life Sciences, and Ph.D. Program in Translational Medicine, National Chung Hsing University, Taichung 402, TaiwanThe maternal-to-zygotic transition (MZT), which controls maternal signaling to synthesize zygotic gene products, promotes the preimplantation development of mouse zygotes to the two-cell stage. Our previous study reported that mouse granzyme g (Gzmg), a serine-type protease, is required for the MZT. In this study, we further identified the maternal factors that regulate the <i>Gzmg</i> promoter activity in the zygote to the two-cell stage of mouse embryos. A full-length <i>Gzmg</i> promoter from mouse genomic DNA, FL-p<i>Gzmg</i> (−1696~+28 nt), was cloned, and four deletion constructs of this <i>Gzmg </i>promoter, Δ1-p<i>Gzmg</i> (−1369~+28 nt), Δ2-p<i>Gzmg</i> (−939~+28 nt), Δ3-p<i>Gzmg</i> (−711~+28 nt) and Δ4-p<i>Gzmg </i>(−417~+28 nt), were subsequently generated. Different-sized <i>Gzmg</i> promoters were used to perform promoter assays of mouse zygotes and two-cell stage embryos. The results showed that Δ4-p<i>Gzmg</i> promoted the highest expression level of the enhanced green fluorescent protein (EGFP) reporter in the zygotes and two-cell embryos. The data suggested that time-specific transcription factors upregulated <i>Gzmg</i> by binding cis-elements in the −417~+28-nt <i>Gzmg</i> promoter region. According to the results of the promoter assay, the transcription factor binding sites were predicted and analyzed with the JASPAR database, and two transcription factors, signal transducer and activator of transcription 3 (STAT3) and GA-binding protein alpha (GABPα), were identified. Furthermore, STAT3 and GABPα are expressed and located in zygote pronuclei and two-cell nuclei were confirmed by immunofluorescence staining; however, only STAT3 was recruited to the mouse zygote pronuclei and two-cell nuclei injected with the Δ4-p<i>Gzmg</i> reporter construct. These data indicated that STAT3 is a maternal transcription factor and may upregulate <i>Gzmg</i> to promote the MZT. Furthermore, treatment with a STAT3 inhibitor, S3I-201, caused mouse embryonic arrest at the zygote and two-cell stages. These results suggest that STAT3, a maternal protein, is a critical transcription factor and regulates <i>Gzmg</i> transcription activity in preimplantation mouse embryos. It plays an important role in the maternal-to-zygotic transition during early embryonic development.https://www.mdpi.com/1422-0067/22/1/460STAT3granzyme gpreimplantation embryomaternal-to-zygotic transition
collection DOAJ
language English
format Article
sources DOAJ
author Huan Ou-Yang
Shinn-Chih Wu
Li-Ying Sung
Shiao-Hsuan Yang
Shang-Hsun Yang
Kowit-Yu Chong
Chuan-Mu Chen
spellingShingle Huan Ou-Yang
Shinn-Chih Wu
Li-Ying Sung
Shiao-Hsuan Yang
Shang-Hsun Yang
Kowit-Yu Chong
Chuan-Mu Chen
STAT3 Is an Upstream Regulator of <i>Granzyme G</i> in the Maternal-To-Zygotic Transition of Mouse Embryos
International Journal of Molecular Sciences
STAT3
granzyme g
preimplantation embryo
maternal-to-zygotic transition
author_facet Huan Ou-Yang
Shinn-Chih Wu
Li-Ying Sung
Shiao-Hsuan Yang
Shang-Hsun Yang
Kowit-Yu Chong
Chuan-Mu Chen
author_sort Huan Ou-Yang
title STAT3 Is an Upstream Regulator of <i>Granzyme G</i> in the Maternal-To-Zygotic Transition of Mouse Embryos
title_short STAT3 Is an Upstream Regulator of <i>Granzyme G</i> in the Maternal-To-Zygotic Transition of Mouse Embryos
title_full STAT3 Is an Upstream Regulator of <i>Granzyme G</i> in the Maternal-To-Zygotic Transition of Mouse Embryos
title_fullStr STAT3 Is an Upstream Regulator of <i>Granzyme G</i> in the Maternal-To-Zygotic Transition of Mouse Embryos
title_full_unstemmed STAT3 Is an Upstream Regulator of <i>Granzyme G</i> in the Maternal-To-Zygotic Transition of Mouse Embryos
title_sort stat3 is an upstream regulator of <i>granzyme g</i> in the maternal-to-zygotic transition of mouse embryos
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1661-6596
1422-0067
publishDate 2021-01-01
description The maternal-to-zygotic transition (MZT), which controls maternal signaling to synthesize zygotic gene products, promotes the preimplantation development of mouse zygotes to the two-cell stage. Our previous study reported that mouse granzyme g (Gzmg), a serine-type protease, is required for the MZT. In this study, we further identified the maternal factors that regulate the <i>Gzmg</i> promoter activity in the zygote to the two-cell stage of mouse embryos. A full-length <i>Gzmg</i> promoter from mouse genomic DNA, FL-p<i>Gzmg</i> (−1696~+28 nt), was cloned, and four deletion constructs of this <i>Gzmg </i>promoter, Δ1-p<i>Gzmg</i> (−1369~+28 nt), Δ2-p<i>Gzmg</i> (−939~+28 nt), Δ3-p<i>Gzmg</i> (−711~+28 nt) and Δ4-p<i>Gzmg </i>(−417~+28 nt), were subsequently generated. Different-sized <i>Gzmg</i> promoters were used to perform promoter assays of mouse zygotes and two-cell stage embryos. The results showed that Δ4-p<i>Gzmg</i> promoted the highest expression level of the enhanced green fluorescent protein (EGFP) reporter in the zygotes and two-cell embryos. The data suggested that time-specific transcription factors upregulated <i>Gzmg</i> by binding cis-elements in the −417~+28-nt <i>Gzmg</i> promoter region. According to the results of the promoter assay, the transcription factor binding sites were predicted and analyzed with the JASPAR database, and two transcription factors, signal transducer and activator of transcription 3 (STAT3) and GA-binding protein alpha (GABPα), were identified. Furthermore, STAT3 and GABPα are expressed and located in zygote pronuclei and two-cell nuclei were confirmed by immunofluorescence staining; however, only STAT3 was recruited to the mouse zygote pronuclei and two-cell nuclei injected with the Δ4-p<i>Gzmg</i> reporter construct. These data indicated that STAT3 is a maternal transcription factor and may upregulate <i>Gzmg</i> to promote the MZT. Furthermore, treatment with a STAT3 inhibitor, S3I-201, caused mouse embryonic arrest at the zygote and two-cell stages. These results suggest that STAT3, a maternal protein, is a critical transcription factor and regulates <i>Gzmg</i> transcription activity in preimplantation mouse embryos. It plays an important role in the maternal-to-zygotic transition during early embryonic development.
topic STAT3
granzyme g
preimplantation embryo
maternal-to-zygotic transition
url https://www.mdpi.com/1422-0067/22/1/460
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