Evidence map›Paper›PMID 26308709›Full record

ArticlePLoS genetics2015

SmD1 Modulates the miRNA Pathway Independently of Its Pre-mRNA Splicing Function.

Xiao-Peng Xiong, Georg Vogler, Krishna Kurthkoti, Anastasia Samsonova, Rui Zhou

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

17 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
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  6. NCells · 2020
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  15. Probing Long Non-coding RNA-Protein Interactions.Frontiers in molecular biosciences · 2017
    Review
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  17. 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

5 authors at 2 institutions in 2 countries.

Xiao-Peng XiongTumor Initiation and Maintenance Program, Sanford-Burnham Medical Research Institute, La Jolla, California, United States of America; Development, Aging and Regeneration Program, Sanford-Burnham Medical Research Institute, La Jolla, California, United States of America.
Georg VoglerDevelopment, Aging and Regeneration Program, Sanford-Burnham Medical Research Institute, La Jolla, California, United States of America.
Krishna KurthkotiTumor Initiation and Maintenance Program, Sanford-Burnham Medical Research Institute, La Jolla, California, United States of America; Development, Aging and Regeneration Program, Sanford-Burnham Medical Research Institute, La Jolla, California, United States of America.
Anastasia SamsonovaDepartment of Oncology, University of Oxford, Oxford, United Kingdom.
Rui ZhouTumor Initiation and Maintenance Program, Sanford-Burnham Medical Research Institute, La Jolla, California, United States of America; Development, Aging and Regeneration Program, Sanford-Burnham Medical Research Institute, La Jolla, California, United States of America.
Sanford Burnham Prebys Medical Discovery Institute · USUniversity of Oxford · GB

Funding

Comprehensive characterization of the Drosophila transcriptomeU01HG004271 · NHGRI · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI CELNIKER, SUSAN E · 2007 to 2011
$18.4M
The Role of microRNAs in Modulating Innate Immunity Signaling and Gut HomeostasisR21AI105797 · NIAID · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI ZHOU, RUI · 2014 to 2015
$536k
NHGRI NIH HHS U01 HG004271NIAID NIH HHS R21 AI105797
6 · The paper itself

Abstract

microRNAs (miRNAs) are a class of endogenous regulatory RNAs that play a key role in myriad biological processes. Upon transcription, primary miRNA transcripts are sequentially processed by Drosha and Dicer ribonucleases into ~22-24 nt miRNAs. Subsequently, miRNAs are incorporated into the RNA-induced silencing complexes (RISCs) that contain Argonaute (AGO) family proteins and guide RISC to target RNAs via complementary base pairing, leading to post-transcriptional gene silencing by a combination of translation inhibition and mRNA destabilization. Select pre-mRNA splicing factors have been implicated in small RNA-mediated gene silencing pathways in fission yeast, worms, flies and mammals, but the underlying molecular mechanisms are not well understood. Here, we show that SmD1, a core component of the Drosophila small nuclear ribonucleoprotein particle (snRNP) implicated in splicing, is required for miRNA biogenesis and function. SmD1 interacts with both the microprocessor component Pasha and pri-miRNAs, and is indispensable for optimal miRNA biogenesis. Depletion of SmD1 impairs the assembly and function of the miRISC without significantly affecting the expression of major canonical miRNA pathway components. Moreover, SmD1 physically and functionally associates with components of the miRISC, including AGO1 and GW182. Notably, miRNA defects resulting from SmD1 silencing can be uncoupled from defects in pre-mRNA splicing, and the miRNA and splicing machineries are physically and functionally distinct entities. Finally, photoactivatable-ribonucleoside-enhanced crosslinking and immunoprecipitation (PAR-CLIP) analysis identifies numerous SmD1-binding events across the transcriptome and reveals direct SmD1-miRNA interactions. Our study suggests that SmD1 plays a direct role in miRNA-mediated gene silencing independently of its pre-mRNA splicing activity and indicates that the dual roles of splicing factors in post-transcriptional gene regulation may be evolutionarily widespread.

Indexed as

AnimalsArgonaute ProteinsBase SequenceCell LineDrosophila melanogasterDrosophila ProteinsGene Expression RegulationGene SilencingInsect ProteinsMicroRNAsRNA-Binding ProteinsRNA-Induced Silencing ComplexRNA, MessengerRNA Processing, Post-TranscriptionalRNA SplicingSequence Analysis, RNAAGO1 protein, DrosophilaArgonaute ProteinsDrosophila ProteinsGw protein, DrosophilaInsect ProteinsMicroRNAsPasha protein, DrosophilaRNA-Binding ProteinsRNA-Induced Silencing ComplexRNA, MessengerSmd1 protein, insect

Identifiers

PMID26308709
PMCPMC4550278
OpenAlexW1866134757

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.