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The role of miRNAs and endogenous siRNAs in maternal-to-zygotic reprogramming and the establishment of pluripotency
P. Svoboda, M. Flemr,
Language English Country England, Great Britain
Document type Journal Article, Research Support, Non-U.S. Gov't, Review
NLK
Free Medical Journals
from 2000 to 1 year ago
PubMed Central
from 2000
Europe PubMed Central
from 2000 to 1 year ago
ProQuest Central
from 2000-07-15 to 2013-11-30
Open Access Digital Library
from 2000-07-01
Medline Complete (EBSCOhost)
from 2000-07-01 to 1 year ago
Health & Medicine (ProQuest)
from 2000-07-15 to 2013-11-30
Public Health Database (ProQuest)
from 2000-07-15 to 2013-11-30
Wiley Free Content
from 2000 to 1 year ago
- MeSH
- Phylogeny MeSH
- Humans MeSH
- RNA, Small Interfering genetics metabolism MeSH
- MicroRNAs classification genetics metabolism MeSH
- Molecular Sequence Data MeSH
- Oocytes cytology physiology MeSH
- Pluripotent Stem Cells cytology physiology MeSH
- RNA Interference MeSH
- Base Sequence MeSH
- Sequence Alignment MeSH
- Animals MeSH
- Zygote cytology physiology MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Review MeSH
RNA silencing is a complex of mechanisms that regulate gene expression through small RNA molecules. The microRNA (miRNA) pathway is the most common of these in mammals. Genome-encoded miRNAs suppress translation in a sequence-specific manner and facilitate shifts in gene expression during developmental transitions. Here, we discuss the role of miRNAs in oocyte-to-zygote transition and in the control of pluripotency. Existing data suggest a common principle involving miRNAs in defining pluripotent and differentiated cells. RNA silencing pathways also rapidly evolve, resulting in many unique features of RNA silencing in different taxonomic groups. This is exemplified in the mouse model of oocyte-to-zygote transition, in which the endogenous RNA interference pathway has acquired a novel role in regulating protein-coding genes, while the miRNA pathway has become transiently suppressed.
References provided by Crossref.org
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