Home LiteratureArticle Details
PMID: 2458285 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Changes in state of adenylation and time course of degradation of maternal mRNAs during oocyte maturation and early embryonic development in the mouse.

Developmental biology ·Vol. 129 ·No. 2 ·1988-10-00 ·Pages 304-14

Paynton BV, Rempel R, Bachvarova R

Abstract

Previous work has shown that more than 50% or about 50 pg of polyadenylated RNA found in the full-grown mouse oocyte is deadenylated or degraded during meiotic maturation. Here we show that rRNA declines by 60 pg during this period, accounting for most of the 80-pg decline in total RNA and indicating that a significant amount of mRNA is deadenylated but not degraded during maturation. Actin mRNA is deadenylated at about 7 hr of in vitro maturation, following the decline in its translation. The poly(A) tail on hypoxanthine phosphoribosyltransferase (HPRT) mRNA is elongated at 7 hr of maturation, preceding an increase in HPRT activity. Actin mRNA is partially degraded in the one-cell embryo and falls to near the limit of detection in the late two-cell stage, while HPRT mRNA shows no change in early two-cell embryos, but is deadenylated and declines greatly during the two-cell stage. In aging unfertilized eggs, most of these changes occur on a delayed schedule. The various species of alpha-tubulin mRNA are largely deadenylated and more than half are degraded during maturation. Taken together with other published results, we conclude that each mRNA has its own pattern of changes in the length of the poly(A) tail (correlated with translation) and degradation during the period of maternal control of protein synthesis, and, for those examined, the maternal mRNAs remaining in the early two-cell embryo are degraded to low levels by the late two-cell stage.

MeSH Terms
Animals Embryonic and Fetal Development Endoribonucleases/metabolism Female Hypoxanthine Phosphoribosyltransferase/genetics Mice Oocytes/growth & development Poly A/metabolism Pregnancy RNA/metabolism RNA, Messenger/metabolism RNA, Ribosomal/analysis Ribonuclease H Time Factors
Chemicals
RNA, Messenger RNA, Ribosomal Poly A RNA Hypoxanthine Phosphoribosyltransferase Endoribonucleases Ribonuclease H
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Paynton B V
Department of Cell Biology and Anatomy, Cornell University Medical College, New York, New York 10021.
Rempel R
Bachvarova R
Article Info
Journal
Developmental biology
Abbr.
Dev Biol
ISSN
0012-1606
Published
1988-10-00
Pages
304-14
Language
English
Region
United States
NLM ID
0372762
Subset
IM
Grants
NICHD NIH HHS · HD 06910 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]