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Winter Hibernation and UCHL1-p34(cdc2) Association in Toad Oocyte Maturation Competence

Currently, it is believed that toad oocyte maturation is dependent on the physiological conditions of winter hibernation. Previous antibody-blocking experiments have demonstrated that toad ubiquitin carboxyl-terminal hydrolase L1 (tUCHL1) is necessary for germinal vesicle breakdown during toad oocyt...

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Autores principales: Kuang, Zhichao, Yao, Yuwei, Shi, Yan, Gu, Zheng, Sun, Zhaogui, Tso, Jiake
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3806854/
https://www.ncbi.nlm.nih.gov/pubmed/24194953
http://dx.doi.org/10.1371/journal.pone.0078785
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author Kuang, Zhichao
Yao, Yuwei
Shi, Yan
Gu, Zheng
Sun, Zhaogui
Tso, Jiake
author_facet Kuang, Zhichao
Yao, Yuwei
Shi, Yan
Gu, Zheng
Sun, Zhaogui
Tso, Jiake
author_sort Kuang, Zhichao
collection PubMed
description Currently, it is believed that toad oocyte maturation is dependent on the physiological conditions of winter hibernation. Previous antibody-blocking experiments have demonstrated that toad ubiquitin carboxyl-terminal hydrolase L1 (tUCHL1) is necessary for germinal vesicle breakdown during toad oocyte maturation. In this paper, we first supply evidence that tUCHL1 is highly evolutionarily conserved. Then, we exclude protein availability and ubiquitin carboxyl-terminal hydrolase enzyme activity as factors in the response of oocytes to winter hibernation. In the context of MPF (maturation promoting factor) controlling oocyte maturation and to further understand the role of UCHL1 in oocyte maturation, we performed adsorption and co-immunoprecipitation experiments using toad oocyte protein extracts and determined that tUCHL1 is associated with MPF in toad oocytes. Recombinant tUCHL1 absorbed p34(cdc2), a component of MPF, in obviously larger quantities from mature oocytes than from immature oocytes, and p13(suc1) was isolated from tUCHL1 with a dependence on the ATP regeneration system, suggesting that still other functions may be involved in their association that require phosphorylation. In oocytes from hibernation-interrupted toads, the p34(cdc2) protein level was significantly lower than in oocytes from toads in artificial hibernation, providing an explanation for the different quantities isolated by recombinant tUCHL1 pull-down and, more importantly, identifying a mechanism involved in the toad oocyte’s dependence on a low environmental temperature during winter hibernation. Therefore, in toads, tUCHL1 binds p34(cdc2) and plays a role in oocyte maturation. However, neither tUCHL1 nor cyclin B1 respond to low temperatures to facilitate oocyte maturation competence during winter hibernation.
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spelling pubmed-38068542013-11-05 Winter Hibernation and UCHL1-p34(cdc2) Association in Toad Oocyte Maturation Competence Kuang, Zhichao Yao, Yuwei Shi, Yan Gu, Zheng Sun, Zhaogui Tso, Jiake PLoS One Research Article Currently, it is believed that toad oocyte maturation is dependent on the physiological conditions of winter hibernation. Previous antibody-blocking experiments have demonstrated that toad ubiquitin carboxyl-terminal hydrolase L1 (tUCHL1) is necessary for germinal vesicle breakdown during toad oocyte maturation. In this paper, we first supply evidence that tUCHL1 is highly evolutionarily conserved. Then, we exclude protein availability and ubiquitin carboxyl-terminal hydrolase enzyme activity as factors in the response of oocytes to winter hibernation. In the context of MPF (maturation promoting factor) controlling oocyte maturation and to further understand the role of UCHL1 in oocyte maturation, we performed adsorption and co-immunoprecipitation experiments using toad oocyte protein extracts and determined that tUCHL1 is associated with MPF in toad oocytes. Recombinant tUCHL1 absorbed p34(cdc2), a component of MPF, in obviously larger quantities from mature oocytes than from immature oocytes, and p13(suc1) was isolated from tUCHL1 with a dependence on the ATP regeneration system, suggesting that still other functions may be involved in their association that require phosphorylation. In oocytes from hibernation-interrupted toads, the p34(cdc2) protein level was significantly lower than in oocytes from toads in artificial hibernation, providing an explanation for the different quantities isolated by recombinant tUCHL1 pull-down and, more importantly, identifying a mechanism involved in the toad oocyte’s dependence on a low environmental temperature during winter hibernation. Therefore, in toads, tUCHL1 binds p34(cdc2) and plays a role in oocyte maturation. However, neither tUCHL1 nor cyclin B1 respond to low temperatures to facilitate oocyte maturation competence during winter hibernation. Public Library of Science 2013-10-23 /pmc/articles/PMC3806854/ /pubmed/24194953 http://dx.doi.org/10.1371/journal.pone.0078785 Text en © 2013 Kuang et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Kuang, Zhichao
Yao, Yuwei
Shi, Yan
Gu, Zheng
Sun, Zhaogui
Tso, Jiake
Winter Hibernation and UCHL1-p34(cdc2) Association in Toad Oocyte Maturation Competence
title Winter Hibernation and UCHL1-p34(cdc2) Association in Toad Oocyte Maturation Competence
title_full Winter Hibernation and UCHL1-p34(cdc2) Association in Toad Oocyte Maturation Competence
title_fullStr Winter Hibernation and UCHL1-p34(cdc2) Association in Toad Oocyte Maturation Competence
title_full_unstemmed Winter Hibernation and UCHL1-p34(cdc2) Association in Toad Oocyte Maturation Competence
title_short Winter Hibernation and UCHL1-p34(cdc2) Association in Toad Oocyte Maturation Competence
title_sort winter hibernation and uchl1-p34(cdc2) association in toad oocyte maturation competence
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3806854/
https://www.ncbi.nlm.nih.gov/pubmed/24194953
http://dx.doi.org/10.1371/journal.pone.0078785
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