Nucleoli in embryos: a central structural platform for embryonic chromatin remodeling?
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem, přehledy
PubMed
30406864
DOI
10.1007/s10577-018-9590-3
PII: 10.1007/s10577-018-9590-3
Knihovny.cz E-zdroje
- Klíčová slova
- Oocyte, chromatin remodeling, embryo, nucleolus, ribosome,
- MeSH
- buněčné jadérko genetika metabolismus MeSH
- chromatin genetika metabolismus MeSH
- embryonální vývoj genetika MeSH
- lidé MeSH
- restrukturace chromatinu * MeSH
- ribozomy genetika metabolismus MeSH
- zárodečné buňky metabolismus MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- přehledy MeSH
- Názvy látek
- chromatin MeSH
Nucleoli are the site of ribosomal RNA production and subunit assembly. In contrast to active nucleoli in somatic cells, where three basic sub-compartments can be observed, mammalian oocytes and early embryos contain atypical nucleoli termed "nucleolus-like bodies" or "nucleolus precursor bodies", respectively. Unlike their somatic counterparts, these structures are composed of dense homogenous fibrillar material and exhibit no polymerase activity. Irrespective of these unusual properties, they have been shown to be absolutely essential for embryonic development, as their microsurgical removal results in developmental arrest. Historically, nucleolus-like and nucleolus precursor bodies have been perceived as passive storage sites of nucleolar material, which is gradually utilized by embryos to construct fully functional nucleoli once they have activated their genome and have started to produce ribosomes. For decades, researchers have been trying to elucidate the composition of these organelles and provide the evidence for their repository role. However, only recently has it become clear that the function of these atypical nucleoli is altogether different, and rather than being involved in ribosome biogenesis, they participate in parental chromatin remodeling, and strikingly, the artificial introduction of a single NPB component is sufficient to rescue the developmental arrest elicited by the NPB removal. In this review, we will describe and summarize the experiments that led to the change in our understanding of these unique structures.
GENNET s r o 170 00 Prague 7 Czech Republic
Institute of Animal Science v v i 104 00 Prague 10 Czech Republic
Institute of Experimental Medicine ASCR v v i 142 20 Prague 4 Czech Republic
Institute of Molecular Genetics ASCR v v i 142 20 Prague 4 Czech Republic
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