The most abundant maternal lncRNA Sirena1 acts post-transcriptionally and impacts mitochondrial distribution
Jazyk angličtina Země Anglie, Velká Británie Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
31956907
PubMed Central
PMC7102984
DOI
10.1093/nar/gkz1239
PII: 5709715
Knihovny.cz E-zdroje
- MeSH
- genový knockout MeSH
- krysa rodu Rattus MeSH
- messenger RNA genetika MeSH
- mitochondrie genetika ultrastruktura MeSH
- myši MeSH
- oocyty růst a vývoj metabolismus ultrastruktura MeSH
- polyadenylace genetika MeSH
- RNA dlouhá nekódující genetika MeSH
- RNA mitochondriální genetika MeSH
- transkriptom genetika MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- messenger RNA MeSH
- mitochondrial messenger RNA MeSH Prohlížeč
- RNA dlouhá nekódující MeSH
- RNA mitochondriální MeSH
Tens of thousands of rapidly evolving long non-coding RNA (lncRNA) genes have been identified, but functions were assigned to relatively few of them. The lncRNA contribution to the mouse oocyte physiology remains unknown. We report the evolutionary history and functional analysis of Sirena1, the most expressed lncRNA and the 10th most abundant poly(A) transcript in mouse oocytes. Sirena1 appeared in the common ancestor of mouse and rat and became engaged in two different post-transcriptional regulations. First, antisense oriented Elob pseudogene insertion into Sirena1 exon 1 is a source of small RNAs targeting Elob mRNA via RNA interference. Second, Sirena1 evolved functional cytoplasmic polyadenylation elements, an unexpected feature borrowed from translation control of specific maternal mRNAs. Sirena1 knock-out does not affect fertility, but causes minor dysregulation of the maternal transcriptome. This includes increased levels of Elob and mitochondrial mRNAs. Mitochondria in Sirena1-/- oocytes disperse from the perinuclear compartment, but do not change in number or ultrastructure. Taken together, Sirena1 contributes to RNA interference and mitochondrial aggregation in mouse oocytes. Sirena1 exemplifies how lncRNAs stochastically engage or even repurpose molecular mechanisms during evolution. Simultaneously, Sirena1 expression levels and unique functional features contrast with the lack of functional importance assessed under laboratory conditions.
Institute of Animal Physiology and Genetics of the Czech Academy of Sciences Libechov Czech Republic
Institute of Molecular Genetics of the Czech Academy of Sciences Prague Czech Republic
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