Evidence map›Paper›PMID 31978041›Full record

ArticlePLoS genetics2020

Makorin 1 controls embryonic patterning by alleviating Bruno1-mediated repression of oskar translation.

Annabelle Dold, Hong Han, Niankun Liu, Andrea Hildebrandt, Mirko Brüggemann, Cornelia Rücklé, Heike Hänel, Anke Busch, Petra Beli, Kathi Zarnack and 3 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

12 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Deciphering the RNA-binding protein network during endosomal mRNA transport.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Makorin RING finger protein 3 and central precocious puberty.Current opinion in endocrine and metabolic research · 2020
    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 4 institutions in 4 countries.

Annabelle DoldRNA Epigenetics, Institute of Molecular Biology, Mainz, Germany.
Hong HanDepartment of Biology, McGill University, Montréal, Québec, Canada.
Niankun LiuDepartment of Biology, McGill University, Montréal, Québec, Canada.
Andrea HildebrandtChromatin Biology and Proteomics, Institute of Molecular Biology, Mainz, Germany.
Mirko BrüggemannBuchmann Institute for Molecular Life Sciences, Goethe University Frankfurt, Frankfurt, Germany.
Cornelia RückléGenomic Views of Splicing Regulation, Institute of Molecular Biology, Mainz, Germany.
Heike HänelGenomic Views of Splicing Regulation, Institute of Molecular Biology, Mainz, Germany.
Anke BuschBioinformatics Core Facility, Institute of Molecular Biology, Mainz, Germany.
Petra BeliChromatin Biology and Proteomics, Institute of Molecular Biology, Mainz, Germany.
Kathi ZarnackBuchmann Institute for Molecular Life Sciences, Goethe University Frankfurt, Frankfurt, Germany.ORCID 0000-0003-3527-3378
Julian KönigGenomic Views of Splicing Regulation, Institute of Molecular Biology, Mainz, Germany.
Jean-Yves RoignantRNA Epigenetics, Institute of Molecular Biology, Mainz, Germany.ORCID 0000-0003-1395-2150
Paul LaskoDepartment of Biology, McGill University, Montréal, Québec, Canada.ORCID 0000-0002-4037-3501
Institute of Molecular Biology · DEGoethe University Frankfurt · DEMcGill University · CARadboud University Nijmegen · NL

Funding

CIHR IOP-107945CIHR MOP-44050
6 · The paper itself

Abstract

Makorins are evolutionary conserved proteins that contain C3H-type zinc finger modules and a RING E3 ubiquitin ligase domain. In Drosophila, maternal Makorin 1 (Mkrn1) has been linked to embryonic patterning but the mechanism remained unsolved. Here, we show that Mkrn1 is essential for axis specification and pole plasm assembly by translational activation of oskar (osk). We demonstrate that Mkrn1 interacts with poly(A) binding protein (pAbp) and binds specifically to osk 3' UTR in a region adjacent to A-rich sequences. Using Drosophila S2R+ cultured cells we show that this binding site overlaps with a Bruno1 (Bru1) responsive element (BREs) that regulates osk translation. We observe increased association of the translational repressor Bru1 with osk mRNA upon depletion of Mkrn1, indicating that both proteins compete for osk binding. Consistently, reducing Bru1 dosage partially rescues viability and Osk protein level in ovaries from Mkrn1 females. We conclude that Mkrn1 controls embryonic patterning and germ cell formation by specifically activating osk translation, most likely by competing with Bru1 to bind to osk 3' UTR.

Indexed as

Body Patterning3' Untranslated RegionsAnimalsCell LineDrosophila melanogasterDrosophila ProteinsFemaleGene Expression Regulation, DevelopmentalHumansIntracellular Signaling Peptides and ProteinsOvaryProtein BindingRNA-Binding Proteins3' Untranslated Regionsbru1 protein, DrosophilaDrosophila ProteinsIntracellular Signaling Peptides and ProteinsMkrn1 protein, Drosophilaosk protein, DrosophilaRNA-Binding Proteins

Identifiers

PMID31978041
PMCPMC7001992
OpenAlexW3002261826

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.