Selective degradation of transcripts during meiotic maturation of mouse oocytes.

Title of Paper:Selective degradation of transcripts during meiotic maturation of mouse oocytes.

Journal:Dev Biol

Place of Publication:USA

Key Words:Oocyte maturation, Metaphase II, Transcriptome, Polyadenylation, Mouse

Summary:There is massive destruction of transcripts during the maturation of mouse oocytes. The objective of this project was to identify and characterize the transcripts that are degraded versus those that are stable during the transcriptionally silent germinal vesicle (GV)-stage to metaphase II (MII)-stage transition using a microarray approach. A system for oocyte transcript amplification using both internal and 3'-poly(A) priming was utilized to minimize the impact of complex variations in transcript polyadenylation prevalent during this transition. Transcripts were identified and quantified using the Affymetrix Mouse Genome 430 v2.0 GeneChip. The significantly changed and stable transcripts were analyzed using Ingenuity Pathways Analysis and GenMAPP/MAPPFinder to characterize the biological themes underlying global changes in oocyte transcripts during maturation. It was concluded that the destruction of transcripts during the GV to MII transition is a selective rather than promiscuous process in mouse oocytes. In general, transcripts involved in processes that are associated with meiotic arrest at the GV-stage and the progression of oocyte maturation, such as oxidative phosphorylation, energy production, and protein synthesis and metabolism, were dramatically degraded. In contrast, transcripts encoding participants in signaling pathways essential for maintaining the unique characteristics of the MII-arrested oocyte, such as those involved in protein kinase pathways, were the most prominent among the stable transcripts.

First Author:You-Qiang Su

Correspondence Author:John J Eppig

All the Authors: Jason Affourtit, Sonya Kamdar, Karen Wigglesworth, Yong Woo,Koji Sugiura

Document Code:10.1016/j.ydbio.2006.09.008

Volume:302

Issue:1

Page Number:104-117

ISSN:0012-1606

Translation or Not:No

Date of Publication:2007-02

Release Time:2025-04-30