Evidence map›Paper›PMID 31956907›Full record

ArticleNucleic acids research2020

The most abundant maternal lncRNA Sirena1 acts post-transcriptionally and impacts mitochondrial distribution.

Sravya Ganesh, Filip Horvat, David Drutovic, Michaela Efenberkova, Dominik Pinkas, Anna Jindrova, Josef Pasulka, Rajan Iyyappan, Radek Malik, Andrej Susor and 3 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.7field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
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  12. microPublication biology · 2022
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  17. Oocyte specific lncRNA variantNon-coding RNA research · 2021
    Article
  18. Review
  19. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 2 countries.

Sravya GaneshInstitute of Molecular Genetics of the Czech Academy of Sciences, Prague, Czech Republic.
Filip HorvatInstitute of Molecular Genetics of the Czech Academy of Sciences, Prague, Czech Republic.
David DrutovicInstitute of Animal Physiology and Genetics of the Czech Academy of Sciences, Libechov, Czech Republic.
Michaela EfenberkovaInstitute of Molecular Genetics of the Czech Academy of Sciences, Prague, Czech Republic.
Dominik PinkasInstitute of Molecular Genetics of the Czech Academy of Sciences, Prague, Czech Republic.
Anna JindrovaInstitute of Animal Physiology and Genetics of the Czech Academy of Sciences, Libechov, Czech Republic.
Josef PasulkaInstitute of Molecular Genetics of the Czech Academy of Sciences, Prague, Czech Republic.
Rajan IyyappanInstitute of Animal Physiology and Genetics of the Czech Academy of Sciences, Libechov, Czech Republic.
Radek MalikInstitute of Molecular Genetics of the Czech Academy of Sciences, Prague, Czech Republic.
Andrej SusorInstitute of Animal Physiology and Genetics of the Czech Academy of Sciences, Libechov, Czech Republic.
Kristian VlahovicekBioinformatics Group, Division of Molecular Biology, Department of Biology, Faculty of Science, University of Zagreb, Croatia.
Petr SolcInstitute of Animal Physiology and Genetics of the Czech Academy of Sciences, Libechov, Czech Republic.
Petr SvobodaInstitute of Molecular Genetics of the Czech Academy of Sciences, Prague, Czech Republic.
Czech Academy of Sciences, Institute of Molecular Genetics · CZCzech Academy of Sciences, Institute of Animal Physiology and Genetics · CZUniversity of Zagreb · HR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

AnimalsGene Knockout TechniquesMiceMitochondriaOocytesPolyadenylationRatsRNA, Long NoncodingRNA, MessengerRNA, MitochondrialTranscriptomemitochondrial messenger RNARNA, Long NoncodingRNA, MessengerRNA, Mitochondrial

Identifiers

PMID31956907
PMCPMC7102984
OpenAlexW3003114853

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.