Evidence map›Paper›PMID 24583175›Full record

ArticleGene2014

U1 small nuclear RNA variants differentially form ribonucleoprotein particles in vitro.

Jason A Somarelli, Annia Mesa, Carol E Rodriguez, Shalini Sharma, Rene J Herrera

Abstract read
In one paragraph

Article in Gene, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. 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.

Jason A Somarelli *Center for RNA Biology and Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC.
Annia Mesa *Department of Biological Sciences, Florida International University, Miami, FL.
Carol E RodriguezDepartment of Biological Sciences, Florida International University, Miami, FL.
Shalini SharmaDepartment of Basic Medical Sciences, University of Arizona, College of Medicine- Phoenix, Phoenix, AZ.
Rene J HerreraHuman and Molecular Genetics, College of Medicine, Florida International University, Miami, FL.

Funding

Theaflavins and Gallic Acid in TeaS06GM008205 · NIGMS · FLORIDA INTERNATIONAL UNIVERSITY · PI BIGGER, CHARLES H · 1989 to 2008
$17.6M
MBRS RESEARCH INITIATIVE FOR SCIENTIFIC ENHANCEMENTR25GM061347 · NIGMS · FLORIDA INTERNATIONAL UNIVERSITY · PI LICKLITER, ROBERT E · 2000 to 2016
$14.7M
Examining role of splicing factor mutations in myelodysplastic syndrome (PQ11)R21CA170786 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SHARMA, SHALINI · 2012 to 2013
$366k
NCI NIH HHS R21 CA170786NIGMS NIH HHS R25 GM061347NIGMS NIH HHS S06 GM008205NIGMS NIH HHS S06 GM08205
6 · The paper itself

Abstract

The U1 small nuclear (sn)RNA participates in splicing of pre-mRNAs by recognizing and binding to 5' splice sites at exon/intron boundaries. U1 snRNAs associate with 5' splice sites in the form of ribonucleoprotein particles (snRNPs) that are comprised of the U1 snRNA and 10 core components, including U1A, U1-70K, U1C and the 'Smith antigen', or Sm, heptamer. The U1 snRNA is highly conserved across a wide range of taxa; however, a number of reports have identified the presence of expressed U1-like snRNAs in multiple species, including humans. While numerous U1-like molecules have been shown to be expressed, it is unclear whether these variant snRNAs have the capacity to form snRNPs and participate in splicing. The purpose of the present study was to further characterize biochemically the ability of previously identified human U1-like variants to form snRNPs and bind to U1 snRNP proteins. A bioinformatics analysis provided support for the existence of multiple expressed variants. In vitro gel shift assays, competition assays, and immunoprecipitations (IPs) revealed that the variants formed high molecular weight assemblies to varying degrees and associated with core U1 snRNP proteins to a lesser extent than the canonical U1 snRNA. Together, these data suggest that the human U1 snRNA variants analyzed here are unable to efficiently bind U1 snRNP proteins. The current work provides additional biochemical insights into the ability of the variants to assemble into snRNPs.

Indexed as

Expressed Sequence TagsGenetic VariationHumansProtein BindingRibonucleoprotein, U1 Small NuclearRNA, Small NuclearRibonucleoprotein, U1 Small NuclearRNA, Small NuclearSNRNP70 protein, humanU1A proteinU1 small nuclear RNASm proteinsSpliceosomeSplicingU1-70K proteinU1A protein

Identifiers

PMID24583175
PMCPMC3997572

What OpenQuestion holds

Textmetadata
LicenceTDM
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.