Evidence map›Paper›PMID 25866926›Full record

ArticleeLife2015

Assessing long-distance RNA sequence connectivity via RNA-templated DNA-DNA ligation.

Christian K Roy, Sara Olson, Brenton R Graveley, Phillip D Zamore, Melissa J Moore

Open access · goldAbstract read
In one paragraph

Article in eLife, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.0field-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

18 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Review
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  4. Review
  5. Article
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  7. Article
  8. Review
  9. Article
  10. Review
  11. Molecular roles and function of circular RNAs in eukaryotic cells.Cellular and molecular life sciences : CMLS · 2018
    Review
  12. Article
  13. The determinants of alternative RNA splicing in human cells.Molecular genetics and genomics : MGG · 2017
    Review
  14. Review
  15. Article
  16. Circular RNAs: analysis, expression and potential functions.Development (Cambridge, England) · 2016
    Review
  17. Article
  18. Splice and sequence.Nature methods · 2015
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 1 country.

Christian K RoyRNA Therapeutics Institute, Howard Hughes Medical Institute, University of Massachusetts Medical School, Worcester, United States.
Sara OlsonInstitute for Systems Genomics, Department of Genetics and Developmental Biology, University of Connecticut Health Center, Farmington, United States.
Brenton R GraveleyInstitute for Systems Genomics, Department of Genetics and Developmental Biology, University of Connecticut Health Center, Farmington, United States.
Phillip D ZamoreRNA Therapeutics Institute, Howard Hughes Medical Institute, University of Massachusetts Medical School, Worcester, United States.
Melissa J MooreRNA Therapeutics Institute, Howard Hughes Medical Institute, University of Massachusetts Medical School, Worcester, United States.
UConn Health · USUniversity of Massachusetts Chan Medical School · USHoward Hughes Medical Institute · US

Funding

Understanding the Mechanism of RNA InterferenceR37GM062862 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI ZAMORE, PHILLIP D · 2010 to 2019
$5.3M
Alternative Splicing of the Drosophilia Dscam Pre-mRNAR01GM067842 · NIGMS · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI GRAVELEY, BRENTON R. · 2003 to 2014
$3.6M
Understanding the Mechanism of RNA Interference (RNAi)R01GM062862 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI ZAMORE, PHILLIP D · 2001 to 2009
$3.2M
NIGMS NIH HHS GM62862NIGMS NIH HHS R01 GM062862NIGMS NIH HHS R01 GM067842NIGMS NIH HHS R37 GM062862
6 · The paper itself

Abstract

Many RNAs, including pre-mRNAs and long non-coding RNAs, can be thousands of nucleotides long and undergo complex post-transcriptional processing. Multiple sites of alternative splicing within a single gene exponentially increase the number of possible spliced isoforms, with most human genes currently estimated to express at least ten. To understand the mechanisms underlying these complex isoform expression patterns, methods are needed that faithfully maintain long-range exon connectivity information in individual RNA molecules. In this study, we describe SeqZip, a methodology that uses RNA-templated DNA-DNA ligation to retain and compress connectivity between distant sequences within single RNA molecules. Using this assay, we test proposed coordination between distant sites of alternative exon utilization in mouse Fn1, and we characterize the extraordinary exon diversity of Drosophila melanogaster Dscam1.

Indexed as

Alternative SplicingBiological AssayRNA EditingAnimalsCell Adhesion MoleculesDNADrosophila melanogasterDrosophila ProteinsEmbryo, NonmammalianExonsFibronectinsGenetic VariationHumansMiceNeural Cell Adhesion MoleculesNucleic Acid HybridizationCell Adhesion MoleculesDNADrosophila ProteinsDscam1 protein, DrosophilaFibronectinsNeural Cell Adhesion MoleculesProtein IsoformsRNA, Long NoncodingRNA Precursorsalternative splicingchromosomesD. melanogasterDscam1fibronectingenesisoformligationmouseRNA-templated

Identifiers

PMID25866926
PMCPMC4442144
OpenAlexW2124665661

What OpenQuestion holds

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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.