Embryonic Cells Redistribute SUMO1 upon Forced SUMO1 Overexpression

ABSTRACT Conjugation of small ubiquitin-like modifiers (SUMOs) to substrate proteins is a posttranslational protein modification that affects a diverse range of physiological processes. Global inhibition of SUMO conjugation in mice results in embryonic lethality, reflecting the importance of the SUM...

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Autores principales: Andreia Lee, Yiping Zhu, Yosef Sabo, Stephen P. Goff
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Publicado: American Society for Microbiology 2019
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spelling oai:doaj.org-article:cce4db26578d48369ff50646e02056402021-11-15T15:54:44ZEmbryonic Cells Redistribute SUMO1 upon Forced SUMO1 Overexpression10.1128/mBio.01856-192150-7511https://doaj.org/article/cce4db26578d48369ff50646e02056402019-12-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mBio.01856-19https://doaj.org/toc/2150-7511ABSTRACT Conjugation of small ubiquitin-like modifiers (SUMOs) to substrate proteins is a posttranslational protein modification that affects a diverse range of physiological processes. Global inhibition of SUMO conjugation in mice results in embryonic lethality, reflecting the importance of the SUMO pathways for embryonic development. Here, we demonstrated that SUMO1 overexpression was not well tolerated in murine embryonic carcinoma and embryonic stem (ES) cells and that only a few clones were recovered after transduction with vectors delivering SUMO1 expression constructs. Differentiated NIH/3T3 cells overexpress SUMO1 without deleterious effects and maintain high levels of both conjugated and free forms of SUMO1. The few embryonic cells surviving after forced overexpression retained all their SUMO1 in the form of a few high-molecular-weight conjugates and maintained undetectable levels of free SUMO1. The absence of free SUMO in embryonic cells was seen specifically upon overexpression of SUMO1, but not SUMO2. Moreover, blocking SUMO1 conjugation to endogenous substrates by C-terminal mutations of SUMO1 or by overexpression of a SUMO1 substrate “sponge” or by overexpression of the deSUMOylating enzyme SUMO-specific peptidase 1 (SENP1) dramatically restored free SUMO1 overexpression. The data suggest that overexpression of SUMO1 protein leading to an excess accumulation of critical SUMO1-conjugated substrates is not tolerated in embryonic cells. Surviving embryonic cells exhibit SUMO1 conjugation to allowed substrates but a complete absence of free SUMO1. IMPORTANCE Embryonic stem (ES) cells exhibit unusual transcriptional, proteomic, and signal response profiles, reflecting their unusual needs for rapid differentiation and replication. The work reported here demonstrated that mouse embryonic cell lines did not tolerate the overexpression of SUMO1, the small ubiquitin-like modifier protein that is covalently attached to many substrates to alter their intracellular localization and functionality. Forced SUMO1 overexpression is toxic to ES cells, and surviving cell populations adapt by dramatically reducing the levels of free SUMO1. Such a response is not seen in differentiated cells or with SUMO2 or with nonconjugatable SUMO1 mutants or in the presence of a SUMO1 “sponge” substrate that accepts the modification. The findings suggest that excess SUMO1 modification of specific substrates is not tolerated by embryonic cells and highlight a distinctive need for these cells to control the levels of SUMO1 available for conjugation.Andreia LeeYiping ZhuYosef SaboStephen P. GoffAmerican Society for MicrobiologyarticleSUMOembryonic stem cellssumoylationposttranslational modificationMicrobiologyQR1-502ENmBio, Vol 10, Iss 6 (2019)
institution DOAJ
collection DOAJ
language EN
topic SUMO
embryonic stem cells
sumoylation
posttranslational modification
Microbiology
QR1-502
spellingShingle SUMO
embryonic stem cells
sumoylation
posttranslational modification
Microbiology
QR1-502
Andreia Lee
Yiping Zhu
Yosef Sabo
Stephen P. Goff
Embryonic Cells Redistribute SUMO1 upon Forced SUMO1 Overexpression
description ABSTRACT Conjugation of small ubiquitin-like modifiers (SUMOs) to substrate proteins is a posttranslational protein modification that affects a diverse range of physiological processes. Global inhibition of SUMO conjugation in mice results in embryonic lethality, reflecting the importance of the SUMO pathways for embryonic development. Here, we demonstrated that SUMO1 overexpression was not well tolerated in murine embryonic carcinoma and embryonic stem (ES) cells and that only a few clones were recovered after transduction with vectors delivering SUMO1 expression constructs. Differentiated NIH/3T3 cells overexpress SUMO1 without deleterious effects and maintain high levels of both conjugated and free forms of SUMO1. The few embryonic cells surviving after forced overexpression retained all their SUMO1 in the form of a few high-molecular-weight conjugates and maintained undetectable levels of free SUMO1. The absence of free SUMO in embryonic cells was seen specifically upon overexpression of SUMO1, but not SUMO2. Moreover, blocking SUMO1 conjugation to endogenous substrates by C-terminal mutations of SUMO1 or by overexpression of a SUMO1 substrate “sponge” or by overexpression of the deSUMOylating enzyme SUMO-specific peptidase 1 (SENP1) dramatically restored free SUMO1 overexpression. The data suggest that overexpression of SUMO1 protein leading to an excess accumulation of critical SUMO1-conjugated substrates is not tolerated in embryonic cells. Surviving embryonic cells exhibit SUMO1 conjugation to allowed substrates but a complete absence of free SUMO1. IMPORTANCE Embryonic stem (ES) cells exhibit unusual transcriptional, proteomic, and signal response profiles, reflecting their unusual needs for rapid differentiation and replication. The work reported here demonstrated that mouse embryonic cell lines did not tolerate the overexpression of SUMO1, the small ubiquitin-like modifier protein that is covalently attached to many substrates to alter their intracellular localization and functionality. Forced SUMO1 overexpression is toxic to ES cells, and surviving cell populations adapt by dramatically reducing the levels of free SUMO1. Such a response is not seen in differentiated cells or with SUMO2 or with nonconjugatable SUMO1 mutants or in the presence of a SUMO1 “sponge” substrate that accepts the modification. The findings suggest that excess SUMO1 modification of specific substrates is not tolerated by embryonic cells and highlight a distinctive need for these cells to control the levels of SUMO1 available for conjugation.
format article
author Andreia Lee
Yiping Zhu
Yosef Sabo
Stephen P. Goff
author_facet Andreia Lee
Yiping Zhu
Yosef Sabo
Stephen P. Goff
author_sort Andreia Lee
title Embryonic Cells Redistribute SUMO1 upon Forced SUMO1 Overexpression
title_short Embryonic Cells Redistribute SUMO1 upon Forced SUMO1 Overexpression
title_full Embryonic Cells Redistribute SUMO1 upon Forced SUMO1 Overexpression
title_fullStr Embryonic Cells Redistribute SUMO1 upon Forced SUMO1 Overexpression
title_full_unstemmed Embryonic Cells Redistribute SUMO1 upon Forced SUMO1 Overexpression
title_sort embryonic cells redistribute sumo1 upon forced sumo1 overexpression
publisher American Society for Microbiology
publishDate 2019
url https://doaj.org/article/cce4db26578d48369ff50646e0205640
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AT yosefsabo embryoniccellsredistributesumo1uponforcedsumo1overexpression
AT stephenpgoff embryoniccellsredistributesumo1uponforcedsumo1overexpression
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