Evidence map›Paper›PMID 17630324›Full record

ArticleRNA (New York, N.Y.)2007

C. elegans sequences that control trans-splicing and operon pre-mRNA processing.

Joel H Graber, Jesse Salisbury, Lucie N Hutchins, Thomas Blumenthal

Open access · bronzeAbstract read
In one paragraph

Article in RNA (New York, N.Y.), 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

27 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Trans-splicing of theDevelopment (Cambridge, England) · 2019
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Transcriptional regulation of gene expression in C. elegans.WormBook : the online review of C. elegans biology · 2013
    Review
  13. Trans-splicing and operons in C. elegans.WormBook : the online review of C. elegans biology · 2012
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Functional analysis of putative operons in Brugia malayi.International journal for parasitology · 2010
    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

4 authors at 3 institutions in 1 country.

Joel H GraberThe Jackson Laboratory, Bar Harbor, ME 04609, USA. joel.graber@jax.org
Jesse Salisbury
Lucie N Hutchins
Thomas Blumenthal
Jackson Laboratory · USUniversity of Colorado Boulder · USUniversity of Maine · US

Funding

WNT SIGNALING IN THE DEVELOPING GASTROINTESTINAL TRACTP20RR016463 · NCRR · MOUNT DESERT ISLAND BIOLOGICAL LAB · PI WRAY, CHRISTOPHER C · 2001 to 2011
$41.0M
TRANS-SPLICING IN C ELEGANSR01GM042432 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI BLUMENTHAL, THOMAS · 1992 to 2011
$3.9M
Translation and Transposons in Mammalian DevelopmentR01HD037102 · NICHD · JACKSON LABORATORY · PI KNOWLES, BARBARA B · 1999 to 2008
$2.9M
Integrated Studies of 3'-UTR Mediated Gene RegulationR01GM072706 · NIGMS · JACKSON LABORATORY · PI GRABER, JOEL H · 2006 to 2009
$986k
Trans-splicing in C. ElegansR56GM042432 · NIGMS · UNIVERSITY OF COLORADO · PI BLUMENTHAL, THOMAS · 2007 to 2007
$360k
NCRR NIH HHS P20 RR016463NCRR NIH HHS P20 RR16463NICHD NIH HHS HD037102NICHD NIH HHS R01 HD037102NIGMS NIH HHS GM072706NIGMS NIH HHS GM42432NIGMS NIH HHS R01 GM042432NIGMS NIH HHS R01 GM072706NIGMS NIH HHS R56 GM042432
6 · The paper itself

Abstract

Many mRNAs in Caenorhabditis elegans are generated through a trans-splicing reaction that adds one of two classes of spliced leader RNA to an independently transcribed pre-mRNA. SL1 leaders are spliced mostly to pre-mRNAs from genes with outrons, intron-like sequences at the 5'-ends of the pre-mRNAs. In contrast, SL2 leaders are nearly exclusively trans-spliced to genes that occur downstream in polycistronic pre-mRNAs produced from operons. Operon pre-mRNA processing requires separation into individual transcripts, which is accomplished by 3'-processing of upstream genes and spliced leader trans-splicing to the downstream genes. We used a novel computational analysis, based on nonnegative matrix factorization, to identify and characterize significant differences in the cis-acting sequence elements that differentiate various types of functional site, including internal versus terminal 3'-processing sites, and SL1 versus SL2 trans-splicing sites. We describe several key elements, including the U-rich (Ur) element that couples 3'-processing with SL2 trans-splicing, and a novel outron (Ou) element that occurs upstream of SL1 trans-splicing sites. Finally, we present models of the distinct classes of trans-splicing reaction, including SL1 trans-splicing at the outron, SL2 trans-splicing in standard operons, competitive SL1-SL2 trans-splicing in operons with large intergenic separation, and SL1 trans-splicing in SL1-type operons, which have no intergenic separation.

Indexed as

AnimalsCaenorhabditis elegansModels, GeneticOperonRNA, HelminthRNA PrecursorsRNA Processing, Post-TranscriptionalRNA, Spliced LeaderRNA Splice SitesTrans-SplicingRNA, HelminthRNA PrecursorsRNA, Spliced LeaderRNA Splice Sites

Identifiers

PMID17630324
PMCPMC1950753
OpenAlexW2148396765

What OpenQuestion holds

Textmetadata
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.