Evidence map›Paper›PMID 27365210›Full record

ArticleRNA (New York, N.Y.)2016

The fission yeast MTREC and EJC orthologs ensure the maturation of meiotic transcripts during meiosis.

Bahjat Fadi Marayati, Victoria Hoskins, Robert W Boger, James F Tucker, Emily S Fishman, Andrew S Bray, Ke Zhang

Open access · bronzeAbstract read
In one paragraph

Article in RNA (New York, N.Y.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-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

7 citing papers in PubMed, 9 citations in OpenAlex.

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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

7 authors at 2 institutions in 1 country.

Bahjat Fadi MarayatiDepartment of Biology and Center for Molecular Communication and Signaling, Wake Forest University, Winston-Salem, North Carolina 27106, USA.
Victoria HoskinsProgram of Human Genetics, Johns Hopkins School of Medicine, Baltimore, Maryland 21205, USA.
Robert W BogerDepartment of Biology and Center for Molecular Communication and Signaling, Wake Forest University, Winston-Salem, North Carolina 27106, USA.
James F TuckerDepartment of Biology and Center for Molecular Communication and Signaling, Wake Forest University, Winston-Salem, North Carolina 27106, USA.
Emily S FishmanDepartment of Biology and Center for Molecular Communication and Signaling, Wake Forest University, Winston-Salem, North Carolina 27106, USA.
Andrew S BrayDepartment of Biology and Center for Molecular Communication and Signaling, Wake Forest University, Winston-Salem, North Carolina 27106, USA.
Ke ZhangDepartment of Biology and Center for Molecular Communication and Signaling, Wake Forest University, Winston-Salem, North Carolina 27106, USA.
Wake Forest University · USJohns Hopkins University · US

Funding

Determination of a Novel Epigenetic Silencing MechanismR15GM119105 · NIGMS · WAKE FOREST UNIVERSITY · PI REID, KE ZHANG · 2016 to 2016
$420k
NIGMS NIH HHS R15 GM119105
6 · The paper itself

Abstract

Meiosis is a highly regulated process by which genetic information is transmitted through sexual reproduction. It encompasses unique mechanisms that do not occur in vegetative cells, producing a distinct, well-regulated meiotic transcriptome. During vegetative growth, many meiotic genes are constitutively transcribed, but most of the resulting mRNAs are rapidly eliminated by the Mmi1-MTREC (Mtl1-Red1 core) complex. While Mmi1-MTREC targets premature meiotic RNAs for degradation by the nuclear 3'-5' exoribonuclease exosome during mitotic growth, its role in meiotic gene expression during meiosis is not known. Here, we report that Red5, an essential MTREC component, interacts with pFal1, an ortholog of eukaryotic translation initiation factor eIF4aIII in the fission yeast Schizosaccharomyces pombe In mammals, together with MAGO (Mnh1), Rnps1, and Y14, elF4AIII (pFal1) forms the core of the exon junction complex (EJC), which is essential for transcriptional surveillance and localization of mature mRNAs. In fission yeast, two EJC orthologs, pFal1 and Mnh1, are functionally connected with MTREC, specifically in the process of meiotic gene expression during meiosis. Although pFal1 interacts with Mnh1, Y14, and Rnps1, its association with Mnh1 is not disrupted upon loss of Y14 or Rnps1. Mutations of Red1, Red5, pFal1, or Mnh1 produce severe meiotic defects; the abundance of meiotic transcripts during meiosis decreases; and mRNA maturation processes such as splicing are impaired. Since studying meiosis in mammalian germline cells is difficult, our findings in fission yeast may help to define the general mechanisms involved in accurate meiotic gene expression in higher eukaryotes.

Indexed as

MeiosisRNA SplicingCarrier ProteinsDEAD-box RNA HelicasesExonsExosome Multienzyme Ribonuclease ComplexExosomesIntronsmRNA Cleavage and Polyadenylation FactorsRNA, MessengerSchizosaccharomycesSchizosaccharomyces pombe ProteinsCarrier ProteinsDEAD-box RNA HelicasesExosome Multienzyme Ribonuclease ComplexMmi1 protein, S pombemRNA Cleavage and Polyadenylation FactorsMtl1 protein, S pombeRed5 protein, S pombeRNA, MessengerSchizosaccharomyces pombe ProteinselF4AIIIexon junction complexMAGOmeiosisMTRECsplicing

Identifiers

PMID27365210
PMCPMC4986891
OpenAlexW2462191533

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.