Ribonucleoprotein localization in mouse oocytes
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't, Review
PubMed
20708690
DOI
10.1016/j.ymeth.2010.08.005
PII: S1046-2023(10)00206-9
Knihovny.cz E-resources
- MeSH
- Embryo, Mammalian chemistry pathology MeSH
- In Situ Hybridization, Fluorescence methods MeSH
- Immunohistochemistry methods MeSH
- Mice MeSH
- Oocytes chemistry pathology MeSH
- Ribonucleoproteins analysis MeSH
- Animals MeSH
- Check Tag
- Mice MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Review MeSH
- Names of Substances
- Ribonucleoproteins MeSH
RNA molecules rarely function alone in cells. For most RNAs, their function requires formation of various ribonucleoprotein (RNP) complexes. For example, mRNP composition can determine mRNA localization, translational repression, level of translation or mRNA stability. RNPs are usually studied by biochemical methods. However, biochemical approaches are unsuitable for some model systems, such as mammalian oocytes and early embryos, due to the small amounts that can be obtained for experimental analysis. In such cases, microscopic techniques are often used to learn about RNPs. Here, we present a review of immunostaining, fluorescence in situ hybridization with subcellular resolution and a combination of both, with emphasis on the mouse oocyte and early embryos models. Application of these techniques to whole-mount fixed oocytes and early embryos can provide information about RNP composition and localization with three-dimensional resolution.
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