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Development and identification of Set transgenic mice
As a multifunctional protein involved in numerous biological processes, Set is expressed in several embryonic and adult organs. Furthermore, Set is overexpressed in numerous types of human cancers, including acute myeloid leukemia, breast cancer and pancreatic cancer. The expression of Set in germ c...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5776649/ https://www.ncbi.nlm.nih.gov/pubmed/29434793 http://dx.doi.org/10.3892/etm.2017.5612 |
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author | Xu, Siliang Liu, Xiaoqiang Gao, Lingling Xu, Boqun Li, Jianmin Gao, Chao Cui, Yugui Liu, Jiayin |
author_facet | Xu, Siliang Liu, Xiaoqiang Gao, Lingling Xu, Boqun Li, Jianmin Gao, Chao Cui, Yugui Liu, Jiayin |
author_sort | Xu, Siliang |
collection | PubMed |
description | As a multifunctional protein involved in numerous biological processes, Set is expressed in several embryonic and adult organs. Furthermore, Set is overexpressed in numerous types of human cancers, including acute myeloid leukemia, breast cancer and pancreatic cancer. The expression of Set in germ cells is involved in gonad development, and the overexpression of Set has been observed in polycystic ovaries. In order to elucidate the physiological and pathological roles of Set, a Set transgenic mouse model was developed, in which the global overexpression of Set in adult tissues could be induced via the Cre/loxP system with the precise deletion of the Stop fragment in double-transgenic hybrids. This result was then confirmed by genotypical and protein analysis using polymerase chain reaction and bioluminescence imaging. In conclusion, the conditional Set transgenic mice carrying a reporter system were successfully generated. The transgenic mice open a new window for the further investigation of the function of Set using tissue-specific Cre mice and inducible Cre systems. |
format | Online Article Text |
id | pubmed-5776649 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-57766492018-02-12 Development and identification of Set transgenic mice Xu, Siliang Liu, Xiaoqiang Gao, Lingling Xu, Boqun Li, Jianmin Gao, Chao Cui, Yugui Liu, Jiayin Exp Ther Med Articles As a multifunctional protein involved in numerous biological processes, Set is expressed in several embryonic and adult organs. Furthermore, Set is overexpressed in numerous types of human cancers, including acute myeloid leukemia, breast cancer and pancreatic cancer. The expression of Set in germ cells is involved in gonad development, and the overexpression of Set has been observed in polycystic ovaries. In order to elucidate the physiological and pathological roles of Set, a Set transgenic mouse model was developed, in which the global overexpression of Set in adult tissues could be induced via the Cre/loxP system with the precise deletion of the Stop fragment in double-transgenic hybrids. This result was then confirmed by genotypical and protein analysis using polymerase chain reaction and bioluminescence imaging. In conclusion, the conditional Set transgenic mice carrying a reporter system were successfully generated. The transgenic mice open a new window for the further investigation of the function of Set using tissue-specific Cre mice and inducible Cre systems. D.A. Spandidos 2018-02 2017-12-11 /pmc/articles/PMC5776649/ /pubmed/29434793 http://dx.doi.org/10.3892/etm.2017.5612 Text en Copyright: © Xu et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Xu, Siliang Liu, Xiaoqiang Gao, Lingling Xu, Boqun Li, Jianmin Gao, Chao Cui, Yugui Liu, Jiayin Development and identification of Set transgenic mice |
title | Development and identification of Set transgenic mice |
title_full | Development and identification of Set transgenic mice |
title_fullStr | Development and identification of Set transgenic mice |
title_full_unstemmed | Development and identification of Set transgenic mice |
title_short | Development and identification of Set transgenic mice |
title_sort | development and identification of set transgenic mice |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5776649/ https://www.ncbi.nlm.nih.gov/pubmed/29434793 http://dx.doi.org/10.3892/etm.2017.5612 |
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