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Peroxiredoxins are required for spindle assembly, chromosome organization, and polarization in mouse oocytes.
Jeon, Hyuk-Joon; Park, Yong Seok; Cho, Dong-Hyung; Kim, Jae-Sung; Kim, Eunji; Chae, Ho Zoon; Chun, Sang-Young; Oh, Jeong Su.
Afiliação
  • Jeon HJ; Department of Genetic Engineering, College of Biotechnology and Bioengineering, Sungkyunkwan University, Suwon, South Korea.
  • Park YS; Department of Genetic Engineering, College of Biotechnology and Bioengineering, Sungkyunkwan University, Suwon, South Korea.
  • Cho DH; Department of East-West Medical Science, Graduate School of East-West Medical Science, Kyung Hee University, Yongin, South Korea.
  • Kim JS; Division of Radiation Cancer Research, Korea Institute of Radiological and Medical Sciences, Seoul, South Korea.
  • Kim E; School of Biological Sciences and Technology, Faculty of Life Science, Chonnam National University, Gwangju, South Korea.
  • Chae HZ; School of Biological Sciences and Technology, Faculty of Life Science, Chonnam National University, Gwangju, South Korea.
  • Chun SY; School of Biological Sciences and Technology, Faculty of Life Science, Chonnam National University, Gwangju, South Korea. Electronic address: sychun@chonnam.ac.kr.
  • Oh JS; Department of Genetic Engineering, College of Biotechnology and Bioengineering, Sungkyunkwan University, Suwon, South Korea. Electronic address: ohjs@skku.edu.
Biochem Biophys Res Commun ; 489(2): 193-199, 2017 07 22.
Article em En | MEDLINE | ID: mdl-28552528
ABSTRACT
Peroxiredoxins (Prxs) are highly conserved antioxidant enzymes and are implicated in multiple biological processes; however, their function in oocyte meiosis has not been studied. Here we show that inhibition of Prx I and II results in spindle defects, chromosome disorganization, and impaired polarization in mouse oocytes. Prx I was specifically localized at the spindle, whereas Prx II was enriched at the oocyte cortex and chromosomes. Inhibition of Prx activity with conoidin A disturbed assembly of the microtubule organizing center (MTOC) through Aurora A regulation, leading to defects in spindle formation. Moreover, conoidin A impaired actin filament and cortical granule (CG) distribution, disrupting actin cap and CG formation, respectively. Conoidin A also increased DNA damage without significantly increasing reactive oxygen species (ROS) levels, suggesting that the effects of conoidin A on meiotic maturation are not likely associated with ROS scavenging pathways. Therefore, our data suggest that Prxs are required for spindle assembly, chromosome organization, and polarization during meiotic maturation.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Oócitos / Polaridade Celular / Cromossomos de Mamíferos / Peroxirredoxinas / Fuso Acromático Limite: Animals Idioma: En Revista: Biochem Biophys Res Commun Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Coréia do Sul

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Oócitos / Polaridade Celular / Cromossomos de Mamíferos / Peroxirredoxinas / Fuso Acromático Limite: Animals Idioma: En Revista: Biochem Biophys Res Commun Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Coréia do Sul