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Generation and identification of a conditional knockout allele for the PSMD11 gene in mice

BACKGROUND: Our previous study have shown that the PSMD11 protein was an important survival factor for cancer cells except for its key role in regulation of assembly and activity of the 26S proteasome. To further investigate the role of PSMD11 in carcinogenesis, we constructed a conditional exon 5 f...

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Autores principales: Zhao, Linlin, Zhao, Jinming, Zhang, Yingying, Wang, Lele, Zuo, Longyan, Niu, Airu, Zhang, Wei, Xue, Xia, Zhao, Suhong, Sun, Chao, Li, Kailin, Wang, Jue, Bian, Zhimin, Zhao, Xiaogang, Saur, Dieter, Seidler, Barbara, Wang, Chuanxin, Qi, Tonggang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7849139/
https://www.ncbi.nlm.nih.gov/pubmed/33517884
http://dx.doi.org/10.1186/s12861-020-00233-1
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author Zhao, Linlin
Zhao, Jinming
Zhang, Yingying
Wang, Lele
Zuo, Longyan
Niu, Airu
Zhang, Wei
Xue, Xia
Zhao, Suhong
Sun, Chao
Li, Kailin
Wang, Jue
Bian, Zhimin
Zhao, Xiaogang
Saur, Dieter
Seidler, Barbara
Wang, Chuanxin
Qi, Tonggang
author_facet Zhao, Linlin
Zhao, Jinming
Zhang, Yingying
Wang, Lele
Zuo, Longyan
Niu, Airu
Zhang, Wei
Xue, Xia
Zhao, Suhong
Sun, Chao
Li, Kailin
Wang, Jue
Bian, Zhimin
Zhao, Xiaogang
Saur, Dieter
Seidler, Barbara
Wang, Chuanxin
Qi, Tonggang
author_sort Zhao, Linlin
collection PubMed
description BACKGROUND: Our previous study have shown that the PSMD11 protein was an important survival factor for cancer cells except for its key role in regulation of assembly and activity of the 26S proteasome. To further investigate the role of PSMD11 in carcinogenesis, we constructed a conditional exon 5 floxed allele of PSMD11 (PSMD11(flx)) in mice. RESULTS: It was found that homozygous PSMD11 (flx/flx) mice showed normal and exhibited a normal life span and fertility, and showed roughly equivalent expression of PSMD11 in various tissues, suggesting that the floxed allele maintained the wild-type function. Cre recombinase could induce efficient knockout of the floxed PSMD11 allele both in vitro and in vivo. Mice with constitutive single allele deletion of PSMD11 derived from intercrossing between PSMD11(flx/flx) and CMV-Cre mice were all viable and fertile, and showed apparent growth retardation, suggesting that PSMD11 played a significant role in the development of mice pre- or postnatally. No whole-body PSMD11 deficient embryos (PSMD11(−/−)) were identified in E7.5–8.5 embryos in uteros, indicating that double allele knockout of PSMD11 leads to early embryonic lethality. To avoid embryonic lethality produced by whole-body PSMD11 deletion, we further developed conditional PSMD11 global knockout mice with genotype Flp;FSF-R26(CAG − CreERT2/+); PSMD11 (flx/flx), and demonstrated that PSMD11 could be depleted in a temporal and tissue-specific manner. Meanwhile, it was found that depletion of PSMD11 could induce massive apoptosis in MEFs. CONCLUSIONS: In summary, our data demonstrated that we have successfully generated a conditional knockout allele of PSMD11 in mice, and found that PSMD11 played a key role in early and postnatal development in mice, the PSMD11 (flx/flx) mice will be an invaluable tool to explore the functions of PSMD11 in development and diseases. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12861-020-00233-1.
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spelling pubmed-78491392021-02-03 Generation and identification of a conditional knockout allele for the PSMD11 gene in mice Zhao, Linlin Zhao, Jinming Zhang, Yingying Wang, Lele Zuo, Longyan Niu, Airu Zhang, Wei Xue, Xia Zhao, Suhong Sun, Chao Li, Kailin Wang, Jue Bian, Zhimin Zhao, Xiaogang Saur, Dieter Seidler, Barbara Wang, Chuanxin Qi, Tonggang BMC Dev Biol Methodology Article BACKGROUND: Our previous study have shown that the PSMD11 protein was an important survival factor for cancer cells except for its key role in regulation of assembly and activity of the 26S proteasome. To further investigate the role of PSMD11 in carcinogenesis, we constructed a conditional exon 5 floxed allele of PSMD11 (PSMD11(flx)) in mice. RESULTS: It was found that homozygous PSMD11 (flx/flx) mice showed normal and exhibited a normal life span and fertility, and showed roughly equivalent expression of PSMD11 in various tissues, suggesting that the floxed allele maintained the wild-type function. Cre recombinase could induce efficient knockout of the floxed PSMD11 allele both in vitro and in vivo. Mice with constitutive single allele deletion of PSMD11 derived from intercrossing between PSMD11(flx/flx) and CMV-Cre mice were all viable and fertile, and showed apparent growth retardation, suggesting that PSMD11 played a significant role in the development of mice pre- or postnatally. No whole-body PSMD11 deficient embryos (PSMD11(−/−)) were identified in E7.5–8.5 embryos in uteros, indicating that double allele knockout of PSMD11 leads to early embryonic lethality. To avoid embryonic lethality produced by whole-body PSMD11 deletion, we further developed conditional PSMD11 global knockout mice with genotype Flp;FSF-R26(CAG − CreERT2/+); PSMD11 (flx/flx), and demonstrated that PSMD11 could be depleted in a temporal and tissue-specific manner. Meanwhile, it was found that depletion of PSMD11 could induce massive apoptosis in MEFs. CONCLUSIONS: In summary, our data demonstrated that we have successfully generated a conditional knockout allele of PSMD11 in mice, and found that PSMD11 played a key role in early and postnatal development in mice, the PSMD11 (flx/flx) mice will be an invaluable tool to explore the functions of PSMD11 in development and diseases. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12861-020-00233-1. BioMed Central 2021-02-01 /pmc/articles/PMC7849139/ /pubmed/33517884 http://dx.doi.org/10.1186/s12861-020-00233-1 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Methodology Article
Zhao, Linlin
Zhao, Jinming
Zhang, Yingying
Wang, Lele
Zuo, Longyan
Niu, Airu
Zhang, Wei
Xue, Xia
Zhao, Suhong
Sun, Chao
Li, Kailin
Wang, Jue
Bian, Zhimin
Zhao, Xiaogang
Saur, Dieter
Seidler, Barbara
Wang, Chuanxin
Qi, Tonggang
Generation and identification of a conditional knockout allele for the PSMD11 gene in mice
title Generation and identification of a conditional knockout allele for the PSMD11 gene in mice
title_full Generation and identification of a conditional knockout allele for the PSMD11 gene in mice
title_fullStr Generation and identification of a conditional knockout allele for the PSMD11 gene in mice
title_full_unstemmed Generation and identification of a conditional knockout allele for the PSMD11 gene in mice
title_short Generation and identification of a conditional knockout allele for the PSMD11 gene in mice
title_sort generation and identification of a conditional knockout allele for the psmd11 gene in mice
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7849139/
https://www.ncbi.nlm.nih.gov/pubmed/33517884
http://dx.doi.org/10.1186/s12861-020-00233-1
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