Actin depolymerization is associated with meiotic acceleration in cycloheximide-treated ovine oocytes

Oocytes treated with the protein synthesis inhibitor cycloheximide (CHX) arrest at the germinal vesicle (GV) stage and undergo accelerated GV breakdown (GVBD) after CHX is removed. However, little is known about the underlying mechanism of accelerated meiotic maturation. Here, we investigated this m...

Full description

Bibliographic Details
Main Authors: German, Sergio D., Lee, Joon-Hee, Campbell, Keith H., Sweetman, Dylan, Alberio, Ramiro
Format: Article
Published: Society for the Study of Reproduction 2015
Subjects:
Online Access:https://eprints.nottingham.ac.uk/37068/
_version_ 1848795386005684224
author German, Sergio D.
Lee, Joon-Hee
Campbell, Keith H.
Sweetman, Dylan
Alberio, Ramiro
author_facet German, Sergio D.
Lee, Joon-Hee
Campbell, Keith H.
Sweetman, Dylan
Alberio, Ramiro
author_sort German, Sergio D.
building Nottingham Research Data Repository
collection Online Access
description Oocytes treated with the protein synthesis inhibitor cycloheximide (CHX) arrest at the germinal vesicle (GV) stage and undergo accelerated GV breakdown (GVBD) after CHX is removed. However, little is known about the underlying mechanism of accelerated meiotic maturation. Here, we investigated this mechanism and found that oocytes released from CHX arrest have higher amounts of cyclin B1 (CCNB1) and phosphorylated mitogen-activated protein kinase (pMAPK) proteins. Increased levels of these factors were not associated with mRNA polyadenylation or increased transcription rates of CCNB1 and MOS (Moloney murine sarcoma viral oncogene homolog) during CHX arrest. We found that treatment of CHX-arrested oocytes with the actin filament-stabilizing agent Jasplakinolide (Jasp) delayed GVBD following release from CHX arrest and that this was correlated with reduced maturation-promoting factor (MPF) activity. These results suggest that CCNB1 mRNAs released from actin filaments during CHX arrest increase CCNB1 transcripts available for translation after release from CHX arrest, leading to the precocious activation of MPF and accelerated meiotic progression.
first_indexed 2025-11-14T19:31:15Z
format Article
id nottingham-37068
institution University of Nottingham Malaysia Campus
institution_category Local University
last_indexed 2025-11-14T19:31:15Z
publishDate 2015
publisher Society for the Study of Reproduction
recordtype eprints
repository_type Digital Repository
spelling nottingham-370682020-05-04T17:04:29Z https://eprints.nottingham.ac.uk/37068/ Actin depolymerization is associated with meiotic acceleration in cycloheximide-treated ovine oocytes German, Sergio D. Lee, Joon-Hee Campbell, Keith H. Sweetman, Dylan Alberio, Ramiro Oocytes treated with the protein synthesis inhibitor cycloheximide (CHX) arrest at the germinal vesicle (GV) stage and undergo accelerated GV breakdown (GVBD) after CHX is removed. However, little is known about the underlying mechanism of accelerated meiotic maturation. Here, we investigated this mechanism and found that oocytes released from CHX arrest have higher amounts of cyclin B1 (CCNB1) and phosphorylated mitogen-activated protein kinase (pMAPK) proteins. Increased levels of these factors were not associated with mRNA polyadenylation or increased transcription rates of CCNB1 and MOS (Moloney murine sarcoma viral oncogene homolog) during CHX arrest. We found that treatment of CHX-arrested oocytes with the actin filament-stabilizing agent Jasplakinolide (Jasp) delayed GVBD following release from CHX arrest and that this was correlated with reduced maturation-promoting factor (MPF) activity. These results suggest that CCNB1 mRNAs released from actin filaments during CHX arrest increase CCNB1 transcripts available for translation after release from CHX arrest, leading to the precocious activation of MPF and accelerated meiotic progression. Society for the Study of Reproduction 2015-03-18 Article PeerReviewed German, Sergio D., Lee, Joon-Hee, Campbell, Keith H., Sweetman, Dylan and Alberio, Ramiro (2015) Actin depolymerization is associated with meiotic acceleration in cycloheximide-treated ovine oocytes. Biology of Reproduction, 92 (4). 103-1-103-9. ISSN 1529-7268 actin depolymerization cyclin B1 cycloheximide cytoskeleton GVBD IVM meiotic arrest meiotic maturation oocyte maturation polyadenylation protein kinases RNA granules http://www.biolreprod.org/content/92/4/103 doi:10.1095/biolreprod.114.122341 doi:10.1095/biolreprod.114.122341
spellingShingle actin depolymerization
cyclin B1
cycloheximide
cytoskeleton
GVBD
IVM
meiotic arrest
meiotic maturation
oocyte maturation
polyadenylation
protein kinases
RNA granules
German, Sergio D.
Lee, Joon-Hee
Campbell, Keith H.
Sweetman, Dylan
Alberio, Ramiro
Actin depolymerization is associated with meiotic acceleration in cycloheximide-treated ovine oocytes
title Actin depolymerization is associated with meiotic acceleration in cycloheximide-treated ovine oocytes
title_full Actin depolymerization is associated with meiotic acceleration in cycloheximide-treated ovine oocytes
title_fullStr Actin depolymerization is associated with meiotic acceleration in cycloheximide-treated ovine oocytes
title_full_unstemmed Actin depolymerization is associated with meiotic acceleration in cycloheximide-treated ovine oocytes
title_short Actin depolymerization is associated with meiotic acceleration in cycloheximide-treated ovine oocytes
title_sort actin depolymerization is associated with meiotic acceleration in cycloheximide-treated ovine oocytes
topic actin depolymerization
cyclin B1
cycloheximide
cytoskeleton
GVBD
IVM
meiotic arrest
meiotic maturation
oocyte maturation
polyadenylation
protein kinases
RNA granules
url https://eprints.nottingham.ac.uk/37068/
https://eprints.nottingham.ac.uk/37068/
https://eprints.nottingham.ac.uk/37068/